Reagents, compositions and methods for improving viability and function of cells, tissues and organs
12419849 ยท 2025-09-23
Assignee
Inventors
Cpc classification
A01N1/126
HUMAN NECESSITIES
A01N1/125
HUMAN NECESSITIES
A61K31/164
HUMAN NECESSITIES
A01N1/128
HUMAN NECESSITIES
International classification
A01N1/125
HUMAN NECESSITIES
A01N1/126
HUMAN NECESSITIES
A01N1/128
HUMAN NECESSITIES
A61K31/164
HUMAN NECESSITIES
Abstract
Compounds, compositions and methods for improving the viability and/or function of cells or for the in vitro, ex vivo or in vivo protection of cells, tissue, graft or organs from various damages are described. The reagents and composition are based on activation of the heat shock response and/or the antioxidant response and include for example, HSP90 co-factor inhibitor such as Celastrol or Celastrol analogs used alone or in combination with an adjunct agent (e.g., a NRF-2 activator, antioxidant, etc.). Therapeutic enhancement may also include increase in paracrine effector production and signaling. Methods for improving the resistance of cells, tissue, grafts or organs to damages or stress, such as hypoxic or oxidative stress-induced cell death, and/or for improving the viability and retention of transplanted or transfused cells are also described. Therapeutic treatment or prevention of ischemic injury (e.g. myocardial infarct, ischemia/reperfusion injury) and related stressors (hypoxia, oxidative stress, inflammation, sepsis/shock, etc) are also provided.
Claims
1. An in vitro or ex vivo method of modulating the state of a cell, a cell preparation, a tissue, a graft or an organ so as to increase resistance to hypoxia reoxygenation stress the method comprising: contacting the cell, the cell preparation, the tissue, the graft or the organ with: a) a composition comprising one or more of the following compounds: ##STR00003## or a pharmaceutically acceptable salt, a stereoisomer, or a tautomer thereof, b) a secretome of: a distinct cell preparation that has been contacted with a composition comprising the one or more of the Analog 1, the Analog 2, the Analog 3, and the Analog 4, or a pharmaceutically acceptable salt, a stereoisomer, or a tautomer thereof or with the combination thereof, wherein the cell or cell preparation is non-cancerous.
2. The method of claim 1, wherein the compound is Analog 1: ##STR00004##
3. The method of claim 1, wherein the compound is Analog 2: ##STR00005##
4. The method of claim 1, wherein the compound is Analog 3: ##STR00006##
5. The method of claim 1, wherein the compound is Analog 4: ##STR00007##
6. The method of claim 1, further comprising contacting the cell, the cell preparation, the tissue, the graft or the organ with: one or more adjunct agent selected from: of tert-butylhydroquinone (tBHQA), bis(2-hydroxybenzylidene) acetone (2HBA), epigallocatechin gallate (EGCG), carnosol, curcumin, ascorbic acid, melatonin, edaravone and andrographolide.
7. The method of claim 1, wherein the cell, tissue, graft or organ is suitable for transplantation in a mammal.
8. The method of claim 7, wherein the mammal suffers from or is susceptible of suffering from an ischemic disease or degenerative disease.
9. The method of claim 8, wherein the ischemic disease is stroke, myocardial infarction (MI), peripheral arterial disease (PAD), transient ischemic attack, microangiopathy, brain ischemia, bowel ischemia, liver ischemia, pulmonary ischemia, renal ischemia, or vascular dementia.
10. The method of claim 1, wherein the method is performed in vitro on cells prior to freezing or during conditioning.
11. The method of claim 1, wherein the cells or the cell preparation comprises stem cells.
12. The method of claim 11, wherein the stem cells are mesenchymal stem cells, CD34+ cells, CD133+ cells, pluripotent, induced pluripotent stem cells, hematopoietic stem cells or progenitor cells.
13. The method of claim 11, wherein the stem cells are autologous stem cells isolated from a mammal in need.
14. The method of claim 11, wherein the stem cells are allogenic stem cells isolated from a mammal donor.
15. The method of claim 14, wherein the allogenic stem cells from the mammal donor is HLA-typed matched, immune-privileged, hypoimmunogenic or immune-evasive with the a mammal in need.
16. The method of claim 1, wherein the method is performed in vitro.
17. The method of claim 16, wherein the method is performed during ex vivo organ perfusion.
18. The method of claim 17, wherein the organ is a heart, kidney, liver or lung.
19. The method of claim 1, wherein the method further comprises transplanting the cell, cell preparation, tissue, graft or organ into a subject in need thereof.
20. A method of transplanting cells, a tissue, a graft or an organ, the method comprising: contacting the cells, tissue, graft or organ with: a) a composition comprising one or more of the following compounds: ##STR00008## or a pharmaceutically acceptable salt, a stereoisomer, or a tautomer thereof, b) a secretome of a distinct cell preparation that has been contacted with a composition comprising the one or more of the Analog 1, the Analog 2, the Analog 3, the Analog 4, or a pharmaceutically acceptable salt, a stereoisomer, or a tautomer or a pro drug thereof or with the combination thereof, wherein the cells, tissue, graft or organ are contacted with the composition in vitro or ex vivo prior to or during a transplant procedure; and wherein the cells are non-cancerous.
21. The method of claim 1, wherein the compound is contacted at a concentration of 10.sup.6 to 10.sup.10 M, and/or wherein the method further comprises washing the cell, cell preparation, tissue, graft or organ after contacting to remove the compound.
22. The method of claim 20, wherein the compound is contacted at a concentration of 10.sup.6 to 10.sup.10 M, and/or wherein the method further comprises washing the stem cells, tissue, graft or organ after contacting to remove the compound.
23. The method of claim 1, wherein the method further comprises washing the cell, the cell preparation, the tissue, the graft or the organ and recuperating the cell, the cell preparation, the tissue, the graft or the organ for up to 24 hours after contacting the cell, the cell preparation, the tissue, the graft or the organ with the composition.
24. The method of claim 21, wherein the method further comprises, adding a long-term storage medium, optionally a cryopreservation media.
25. The method of claim 1, wherein the composition is contacted for between 5 minutes to 4 hours.
26. An in vitro or ex vivo method of modulating the state of a cell, a cell preparation, a tissue, a graft or an organ so as to increase resistance to hypoxic stress the method comprising contacting the cell, the cell preparation, the tissue, the graft or the organ with: a) a composition comprising one or more of the following compounds: ##STR00009## or a pharmaceutically acceptable salt, a stereoisomer, or a tautomer thereof, b) a secretome of: a distinct cell preparation that has been contacted with a composition comprising the one or more of the Analog 1, the Analog 2, and the Analog 3, or a pharmaceutically acceptable salt, a stereoisomer, or a tautomer thereof or with the combination thereof, wherein the cell or cell preparation is non-cancerous.
27. The method of claim 26, further comprising contacting the cell, the cell preparation, the tissue, the graft or the organ with: one or more adjunct agent selected from: of tert-butylhydroquinone (tBHQ), bis(2-hydroxybenzylidene) acetone (2HBA), epigallocatechin gallate (EGCG), carnosol, curcumin, ascorbic acid, melatonin, edaravone and andrographolide and/or wherein the cell, tissue, graft or organ is suitable for transplantation in a mammal.
28. The method of claim 27, wherein the mammal suffers from or is susceptible of suffering from an ischemic disease or degenerative disease.
29. The method of claim 28, wherein the ischemic disease is stroke, myocardial infarction (MI), peripheral arterial disease (PAD), transient ischemic attack, microangiopathy, brain ischemia, bowel ischemia, liver ischemia, pulmonary ischemia, renal ischemia, or vascular dementia.
30. The method of claim 26, wherein the method is performed in vitro on cells prior to freezing or during conditioning and/or wherein the cells or the cell preparation comprises stem cells.
31. The method of claim 30, wherein the stem cells are mesenchymal stem cells, CD34+ cells, CD133+ cells, pluripotent, induced pluripotent stem cells, hematopoietic stem cells or progenitor cells, wherein the stem cells are autologous stem cells isolated from a mammal in need, or wherein the stem cells are allogenic stem cells isolated from a mammal donor.
32. The method of claim 31, wherein the allogenic stem cells from the mammal donor is HLA-typed matched, immune-privileged, hypoimmunogenic or immune-evasive with the a mammal in need.
33. The method of claim 26, wherein the method is performed in vitro or performed during ex vivo organ perfusion and/or wherein the organ is a heart, kidney, liver or lung.
34. The method of claim 26, wherein the method further comprises transplanting the cell, cell preparation, tissue, graft or organ into a subject in need thereof and/or wherein the composition is contacted for between 5 minutes to 4 hours.
Description
BRIEF DESCRIPTION OF DRAWINGS
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DISCLOSURE OF INVENTION
(46) In the present application, the Applicant showed that Celastrol may be useful to protect cells and tissue from different kinds of damages and may increase the survival of cells that are part of complex tissues, such as grafts and organs. For example, stems cells pre-conditioned with Celastrol alone or in combination with an adjunct agent protect cells from stress and/or damages and stimulate secretion of paracrine mediators and growth factors that enhance the therapeutic profile of cells.
(47) The Applicant also identified Celastol analogues having similar or increased cytoprotective effect and identified several therapeutic combinations having synergistic or additive cytoprotective effects with Celastrol and/or with Celastrol analogues.
(48) Celastrol's mechanisms of Induction of HSR and anti-oxidant response, leading to upregulation of cytoprotective HPSs is schematized in
(49) More particularly, Celastrol mechanism of action includes 1) activation of the rapid and transient cellular defense mechanism. More particularly, Celastrol modulates activity of KEAP1, the repressor of the transcription factor Nuclear Factor Erythroid 2-Related Factor 2 (NRF2), thereby allowing translocation of NRF2 to the nucleus and binding to ARE (Antioxidant Response Element) which activates transcription of protective antioxidant mediators and enzymes including HO1 (HSP32).
(50) Celastrol mechanism of action also includes 2) activation of the cellular pathway ensuring extended protection and survival: Celastrol antagonises the essential co-chaperones of HSP90, namely Cdc37, which results in dissociation of the HSF1 from its chaperone repressor HSP90. This leads to HSF1 phosphorylation, trimerization, nuclear translocation and binding to HSE (Heat Shock Element) thereby inducing de novo transcription of cytoprotective Heat Shock Proteins (HSP) including HSP27, HSP32 and HSP70.
(51) Celastrol mechanism of action may further include 3) induction/amplification of protective signaling: Celastrol by stimulating ROS production may activate above described mechanisms thereby leading to activation of protective signaling pathways.
(52) The use of the terms a and an and the and similar referents in the context of describing the invention (especially in the context of the claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context.
(53) The terms comprising, having, including, and containing are to be construed as open-ended terms (i.e., meaning including, but not limited to) unless otherwise noted.
(54) Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if It were individually recited herein. All subsets of values within the ranges are also incorporated into the specification as if they were individually recited herein.
(55) Similarly, herein a general chemical structure with various substituents and various radicals enumerated for these substituents is intended to serve as a shorthand method of referring individually to each and every molecule obtained by the combination of any of the radicals for any of the substituents. Each individual molecule is incorporated into the specification as if it were Individually recited herein. Further, all subsets of molecules within the general chemical structures and all structures/molecules belonging to the same compound family are also incorporated into the specification as if they were individually recited herein.
(56) Any and all combinations and subcombinations of the embodiments and features disclosed herein are encompassed by the present invention.
(57) Herein, the term about has its ordinary meaning. The term about is used to indicate that a value includes an inherent variation of error for the device or the method being employed to determine the value, or encompass values close to the recited values, for example within 10% or 5% of the recited values (or range of values).
(58) All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context.
(59) The use of any and all examples, or exemplary language (e.g., such as) provided herein, is intended merely to better illustrate the invention and does not pose a limitation on the scope of the invention unless otherwise claimed.
(60) Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.
(61) The present invention provides a method of Improving the resistance of cells to cell death (e.g., resistance to oxidative and/or hypoxic stress induced death, other physical or chemical or mechanical stressors including heat, oxidation, H.sub.2O.sub.2, hypoxia, encapsulation, etc.), said method comprising contacting the cells with an effective amount of one or more compounds that activate the HSF1 pathway and the NRF2 pathway. The present invention provides the use one or more compounds that activate the HSF1 pathway and the NRF2 pathway for improving the resistance of cells to cell death and improving cellular functionality.
(62) The present invention also provides a method of improving the viability and retention of transplanted or transfused cells, said method comprising contacting the cells with an effective amount of one or more compounds that activate the HSF1 pathway and the NRF2 pathway prior to and/or after transplantation or transfusion.
(63) The present Invention also provides a method of improving the therapeutic profile and functionality of stem cells (activation of beneficial proteins including growth factors, antioxidant enzymes, heat shock proteins, chemokines and anti-inflammatory cytokines for paracrine amelioration of transplant microenvironment), said method comprising contacting the stem cells with an effective amount of one or more compounds that activate the HSF1 pathway and the NRF2 pathway.
(64) The present invention also provides a method of Identifying one or more compounds that may be useful for improving the resistance of cells to cell death (e.g., hypoxic and/or oxidative and/or hypoxia/reoxygenation stress-induced cell death) and/or improving the viability and retention of transplanted or transfused cells, said method comprising (i) contacting a cell with said one or more compounds; (H) determining whether the HSF1 pathway and the NRF2 pathway are activated in said cell, wherein activation of said pathway is indicative that said one or more compounds may be useful for improving the resistance of cells to cell death and/or improving the viability and retention of transplanted or transfused cells.
(65) The present invention also provides a method of treating a subject in need of cell transplantation or transfusion, said method comprising (a) contacting the cells to be transplanted with an effective amount of one or more compounds that activate the HSF1 pathway and the NRF2 pathway; and (b) transplanting or transfusing the cells of (a) in said subject.
(66) The expression compound that activates the Heat shock factor protein 1 (HSF1) pathway refers to any agent (small molecules, peptides, proteins, antibodies, oligomers, etc.) capable of directly or indirectly increasing the release of HSF1 from the chaperone repressor HSP90 complex and/or activating its translocation to the nucleus or increasing its cellular content, thus increasing HSF1-mediated transcription. It includes agents that antagonizes the co-chaperone(s) of HSP90, such as Cdc37 and p23, which results in dissociation/activation of HSF1 or HSF1 protein itself.
(67) The expression compound that activates the Nuclear factor (erythroid-derived 2)-like 2 (NRF2) pathway refers to any agent (small molecules, peptides, antibodies, oligomers, etc.) capable of directly or indirectly increasing the release of NRF2 from the repressor Kelch-like ECH-associated protein 1 (KEAP1) and/or activating its translocation to the nucleus or increasing its cellular content, thus increasing NRF2-mediated transcription. KEAP1 comprises six Kelch repeats (residues 327-372, 373-423, 424-470, 471-517, 518-564 and 565-611) that mediate Interaction with NRF2. Residues 69-84, and more particularly residues 76-84, of NRF2 (which encompass the conserved ETGE motif), are involved in the interaction with KEAP1. Examples of compounds that activate the NRF2 pathway include Celastrol, tBHQ, CDDO, Camosol, Andrographolide, Cafestol, Sulforaphane, Curcumin, EGCG, Pyrithione, Resveratrol, Gedunin, Quercetin, bis(2-hydroxybenzylidene)acetone (2-HBA) or HBB2, 1,2-dithiole-3-thione (D3T), acetylenic tricyclic bis(cyano enone) (TBE31), Anthothecol, Whitanolides, and analogs thereof or members of alkaloid, quinones and quinone methide, gambogic acid, limonoids, rotenoids, terpenoids, furanoids, cathechins, alkenyls, carbohydrates, flavonoids, or aromatic families.
(68) In an embodiment, the method comprises the use of one compound that activates both the HSF1 pathway and the NRF2 pathway. In another embodiment, the method comprises the use of two or more molecules that activate the HSF1 pathway and the NRF2 pathway, e.g. a first compound that activates the HSF1 pathway and a second compound that activates the NRF2 pathway, or a first compound that activates the HSF1 and NRF2 pathways and a second compound that activates only the NRF2 pathway, etc.
(69) In an embodiment, the one or more compounds comprises Celastrol or an analog thereof, a compound of the withanolide family (e.g. Withanolide A, Withaferin A) or an analog thereof, a compound of the limonoid family (e.g., Gedunin) or an analog thereof, a curcuminoid (e.g., Curcumin) or an analog thereof, Sulforaphane or an analog thereof, sulphoxythiocarbamate alkyne (STCA) or an analog thereof, Novobiocin or an analog thereof, Lonidamine or an analog thereof, Gamendazole or an analog thereof, a Bardoxolone/CDDO compound (e.g. CDDO-Im) or an analog thereof, tert-Butylhydroquinone (tBHQ) or an analog thereof, (1E,4E)-1,5-Bis(2-Hydroxyphenyl)-1,4-pentadien-3-one (HBB2) or an analog thereof, acetylenic tricyclic bis(cyano enone) (TBE-31) or an analog thereof, epigallocatechin gallate (EGCG) or an analog thereof, or any combination thereof. The term analog as used herein refers to a compound having the basic or backbone structure of the reference compound, but comprising one or more modifications (e.g., bond order, absence or presence of one or more atoms and/or groups of atoms, and combinations thereof) that do not abolish the biological activity on the HSF1 pathway and/or the NRF2 pathway. For example, Celastrol analogs (pentacyclic triterpene compounds) are described in Klaic et al., ACS Chem Biol. 2012 May 18; 7(5): 928-937 and PCT publication No. WO2015/148802.
(70) In an embodiment, at least one of the one or more compounds is an HSP90 inhibitor, an HSP90 N or C-terminal Inhibitor, preferably an HSP90 co-factor Inhibitor.
(71) In an embodiment, at least one of the one or more compounds has NRF2 inducing activity.
(72) In an embodiment, a combination of compounds having improved (e.g., synergistic) activity relative to activity of the compounds used alone are used. Examples of combinations of compounds include (i) (a) Celastrol or an analog thereof; and (b) EGCG or an analog thereof; (ii) (a) Celastrol or an analog thereof; and (b) tBHQ or an analog thereof; (Iii) (a) Gedunin or an analog thereof; and (b) EGCG or an analog thereof; (iv) (a) Gedunin or an analog thereof; and (b) tBHQ or an analog thereof; (v) (a) Celastrol or an analog thereof; and (b) 2HBA or an analog thereof; (vi) (a) Celastrol or an analog thereof; and (b) Curcumin or an analog thereof; or (vii) a) Celastrol or an analog thereof; and (b) Camosol or an analog thereof.
(73) As used herein the term adjunct agent refers an agent that may increase cell survival, viability or resistance to stress or damages. An adjunct agent may be capable of modulating for example cell phenotype and may Include antioxidants and NRF2 activators. Adjunct agents include for example, 2HBA, andrographolide, ascorbic acid, cafestol, camosolbardoxolone-imidazole (CDDO-im), chalcone, N6-[2-[[4-(2,4-dichlorophenyl)-5-(1H-imidazol-2-yl)-2-pyrimidinyl]amino]ethyl]-3-nitro-2,6-pyridinediamine (CHIR98014), conglobatin, curcumin, cycloastragenol, 1,2-dithiole-3-thione (D3T), doramapimod, edaravone, EGCG, gambogic acid, ganetespib, gedunin, IQ-1, limonin, lonidamide, melatonin, benzamide tetrahydroindolones, N886, alkylamino biphenylamides, novobiocin, pyridoxal 5-phosphate (P5-P), pyrithione, quercetin, radicicol, resveratrol, N-(2-cyano-3,12-dioxo-28-noroleana-1,9(11)-dien-17-yl)-2,2-difluoro-propanamide or omaveloxolone (RTA-408), 4-(4-Fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)-1H-imidazole (SB202190), 3-(2,4-Dichlorophenyl)-4-(1-methyl-1H-indol-3-yl)-1H-pyrrole-2,5-dione (SB216763), SNX-5422 (PF-04929113), sodium Butyrate, sulforane, tetrabromobenzotriazole (TBB), tert-butylhydroquinone (tBHQ), valporic acid, withaferin A, ergosterols, lupenones and analogs of any such adjunct agents.
(74) As used herein the term secretome refers to secreted organic molecules and/or inorganic elements by biological cells, tissues, organs, and organisms.
(75) As used herein the expression modulating the state of a cell means a change in the cellular phenotype, in the pattern of expression of certain genes or in the pattern of secretion of certain proteins.
(76) The expression straight alkyl group of 1 to 6 carbon atoms (i.e., C1-C6 alkyl) as used herein means saturated monovalent hydrocarbon radicals having straight or branched moieties and containing from 1 to 6 carbon atoms. The term branched alkyl group refers to alkyl group that include one or more tertiary or quaternary carbon atoms.
(77) The alkyl group may be substituted (OH, NH2, I, F, Cl, Br, CN) unsubstituted. Examples of such groups include, but are not limited to, methyl, ethyl, propyl, iso-propyl, n-butyl, iso-butyl, and tert-butyl.
(78) As used herein, the term substituted refers to a group in which one or more hydrogen atoms in the group are, independently, replaced with a substituent selected from methyl, ethyl, n-propyl, isopropyl, hydroxy, methoxy, ethoxy, fluorine, chlorine, bromine, iodine, cyano, nitro, amino, alkylamino, dialkylamino, carboxy, chloromethyl, trichloromethyl, trifluoromethyl, methoxyethyl and the like.
(79) As used herein the term lower alkyl group of 1 to 3 carbon atoms refers to methyl, ethyl, propyl.
(80) In an embodiment, the one or more compounds are present in a pharmaceutical composition that further comprises one or more pharmaceutically acceptable carriers, excipient, and/or diluents. As used herein, pharmaceutically acceptable (or biologically acceptable) refers to materials characterized by the absence of (or limited) toxic or adverse biological effects in vivo. It refers to those compounds, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the biological fluids and/or tissues and/or organs of a subject (e.g., human, animal) without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.
(81) The term pharmaceutically acceptable carriers, excipient, and/or diluents refers to additives commonly used in the preparation of pharmaceutical compositions and includes, for example, solvents, dispersion media, saline solutions, surfactants, solubilizing agents, lubricants, emulsifiers, coatings, antibacterial and antifungal agents, chelating agents, pH-modifiers, soothing agents, buffers, reducing agents, antioxidants, isotonic agents, absorption delaying agents or the like (see, e.g., Rowe et al., Handbook of Pharmaceutical Excipients, Pharmaceutical Press; 6.sup.th edition, 2009).
(82) In an embodiment, the one or more compounds may be combined/mixed with scaffold materials for cell transplantation/tissue engineering, e.g., biomaterials, polymers and/or matrixes commonly used as scaffold for stem cells.
(83) The one or more compounds may be formulated for administration via any conventional route, such as intravenous, oral, transdermal, intraperitoneal, subcutaneous, mucosal, Intramuscular, Intranasal, Intrapulmonary, parenteral or topical administration. The preparation of such formulations is well known in the art (see, e.g., Remington: The Science and Practice of Pharmacy, Lippincott Williams & Wilkins; 21.sup.st edition, 2005).
(84) Also, as shown in the Examples below, the medium (e.g., secretome) from cells treated with the one or more compounds was able to confer protection against death, and thus in an embodiment the methods described herein comprises culturing a population of cells (e.g., mesenchymal stem cells, CD133.sup.+ cells, pancreatic cells, renal cells, epithelial and endothelial cells) In the presence of the one or more compounds, collecting the medium or supernatant from said culture; and contacting cells in the presence of said medium or supernatant.
(85) In an embodiment, the cell is a stem/pluripotent/progenitor cell or differentiated cell, for example an hematopoietic stem cell (HSC), an hematopoletic progenitor cells (HPCs), a multipotent progenitor cell (MPP), a lymphoid progenitor cell, a myeloid progenitor cell, a mesenchymal stem cell (MSC), an adipose derived stem cell (ADSC), etc. In another embodiment, the cell is a differentiated cell.
(86) The starting population of cells may be obtained from the body or an organ of the body containing suitable cells. The cells collected can be enriched for cells having certain characteristics in ways known to those of skill in the art, for example based on expression of certain markers (e.g., CD34.sup.+, CD133.sup.+). Moreover, the starting cell population may be used directly or frozen and stored for use at a later point in time. Thus, the cell population may first be subjected to enrichment or purification steps, including adhesion to plasticware or negative and/or positive selection of cells based on specific cellular markers in order to provide the starting cell population, for example to provide a starting cell population enriched in MSCs. Methods for isolating said starting cell population based on specific cellular markers may use fluorescent-activated cell sorting (FACS) technology or solid or insoluble substrate to which Is bound antibodies or ligands that interact with specific call surface markers. For example, cells may be contacted with a solid substrate (e.g., column of beads, flasks, magnetic particles) containing the antibodies and any unbound cells are removed. When a solid substrate comprising magnetic or paramagnetic beads is used, cells bound to the beads can be readily isolated by a magnetic separator (e.g. magnetic cell sorting, MACS, CliniMacs product line by Miltenyi Biotec).
(87) The cells may be cultured in media suitable for the maintenance, growth, or proliferation of the cells either in normal culture conditions of bioreactors for large scale manufacturing for example. The culture conditions of the population of cells will vary depending on different factors, notably, the starting cell population. Suitable culture media and conditions are well known in the art. The method of the present invention may be carried out in natural medium, a semi-synthetic medium or a synthetic medium in terms of composition, and may be a solid medium, a semisolid medium or a liquid medium in terms of shape, and any nutrient medium or defined medium used for cell culture, which may be supplemented with one or more suitable factors. Such medium typically comprises sodium, potassium, calcium, magnesium, phosphorus, chlorine, amino acids, vitamins, cytokines, hormones, antibiotics, serum, fatty acids, saccharides or the like. In the culture, other chemical components or biological components may be incorporated singly or in combination, as the case requires. Such components to be incorporated in the medium may be fetal calf serum, human serum, horse serum, insulin, transferrin, lactoferrin, cholesterol, ethanolamine, sodium selenite, monothioglycerol, 2-mercaptoethanol, bovine serum albumin, sodium pyruvate, polyethylene glycol, various vitamins, various amino acids, agar, agarose, collagen, methylcellulose, various cytokines, various growth factors or the like. The media may be chemically defined, serum-free and/or xeno-free.
(88) During or following treatment with the one or more compounds, the cells may be cultured under conditions suitable for their maintenance, growth and/or proliferation.
(89) The amount of the one or more compounds used to mediate the above-noted effects may be determined by the skilled person. In an embodiment, the concentration is about 1 nM to about 1 mM, about 10 nM to 100 M, or about 100 nM to about 10 M.
(90) Concentrations of 10.sup.5 M to 10.sup.10 M (including individually, from 1 uM to 10 uM, from 5 uM to 10 mM) are also encompassed by the present Invention.
(91) In an embodiment, the above-noted contacting comprises the addition of a single dose or multiple doses of the one or more compounds in the culture medium.
(92) The treatments with compounds may be administered in vivo, in the patient and cells, tissues, organs, and then may be collected as described above
(93) The cell population may then be washed to remove the one or more compounds and/or any other component of the cell culture and resuspended in an appropriate cell suspension medium, either washed off or left in contact for short term use or in a long-term storage medium, for example a medium suitable for cryopreservation.
(94) Subjects that may benefit from transplantation/transfusion of cells, and more particularly stem cells, include subjects suffering from heart failure, stenocardia, cardiac infarction (e.g., heart/cardiac ischemia), arrhythmia, valvular heart diseases, myocardial/pericardial diseases, congenital heart diseases (e.g., atrial septal defect, ventricular septal defect, arterial duct patency, tetralogy of Fallot), arterial diseases (e.g., arterial sclerosis, aneurysm, etc.). venous diseases (e.g., phlebeurysm), critical limb or organ ischemia (hepatic ischemia, etc.), degenerative joint disease, osteoarthritis, rheumatoid arthritis, bone disorders (e.g., osteitis, osteoporosis, osteoarthritis, osteosarcoma), skin disorders (e.g., psoriasis, eczema, skin cancer), corneal diseases (e.g., keratoconus, keratitis), liver diseases (e.g., acute and chronic liver failure, hepatitis, genetic deficiency including urea cycle disorder), lung diseases (e.g., COPD, ARDS, pneumonitis), kidney diseases (e.g., CKD), musculoskeletal injuries, tendinitis, systemic disease (e.g. sepsis), cancer, disorders, degenerative diseases including CNS diseases (e.g. Alzheimers, Parkinsons, Dementia, ALS) and spinal injuries.
(95) The one or more compounds may be used in combination with other therapies/drugs used for the treatment of the above-mentioned diseases/disorders/conditions. The one or more compounds may be administered or co-administered (e.g., consecutively, simultaneously, at different times) in any conventional dosage form. Co-administration in the context of the present invention refers to the administration of more than one therapeutic in the course of a coordinated treatment to achieve an improved clinical outcome. Such co-administration may also be coextensive, that is, occurring during overlapping periods of time. For example, the one or more compounds may be administered to the subject before, concomitantly, before and after, or after the additional active agent or therapy is administered. The active agents (e.g., the one or more compounds and the additional active agent) may in an embodiment be combined/formulated in a single composition and thus administered at the same time.
(96) Any suitable amount of the one or more compounds or pharmaceutical composition comprising same may be administered to a subject. The dosages and frequency of administration will depend on many factors including the mode of administration. For the prevention, treatment or reduction in the severity of a given disease or condition, the appropriate dosage of the one or more compounds/composition will depend on the type of disease or condition to be treated, the severity and course of the disease or condition, whether the compound/composition is administered for preventive or therapeutic purposes, previous therapy, the patient's clinical history and response to the compound/composition, and the discretion of the attending physician. The compound/composition is suitably administered to the patient at one time or over a series of treatments. Preferably, it is desirable to determine the dose-response curve in vitro, and then in useful animal models prior to testing in humans. The present invention provides dosages for the compounds and compositions comprising same. For example, depending on the type and severity of the disease, about 1 g/kg to to 1000 mg per kg (mg/kg) of body weight per day. Further, the effective dose may be about 0.1 mg/kg, 0.2 mg/kg, 0.3 mg/kg, 0.4 mg/kg, 0.5 mg/kg, 1 mg/kg, 5 mg/kg, 10 mg/kg, 15 mg/kg, 20 mg/kg/25 mg/kg, 30 mg/kg, 35 mg/kg, 40 mg/kg, 45 mg/kg, 50 mg/kg, 55 mg/kg, 60 mg/kg, 70 mg/kg, 75 mg/kg, 80 mg/kg, 90 mg/kg, 100 mg/kg, 125 mg/kg, 150 mg/kg, 175 mg/kg or 200 mg/kg, and may Increase by 25 mg/kg increments up to 1000 mg/kg, or may range between any two of the foregoing values. A typical daily dosage might range from about 1 g/kg to 100 mg/kg or more, depending on the factors mentioned above. For repeated administrations over several days or longer, depending on the condition, the treatment is sustained until a desired suppression of disease symptoms, or clinical endpoint, occurs. The one or more compounds may be administered at the appropriate frequency, e.g., once, once-a-day, twice weekly, weekly, every two weeks, every month However, other dosage regimens may be useful. The progress of this therapy is easily monitored by conventional techniques and assays. These are simply guidelines since the actual dose must be carefully selected and titrated by the attending physician based upon clinical factors unique to each patient. The optimal dose will be determined by methods known in the art and will be Influenced by factors such as the age of the patient and other clinically relevant factors. In addition, patients may be taking medications for other diseases or conditions.
(97) Similarly, when pre-conditioned cells are administered to a patient, the number of cells transfused will take into consideration factors such as sex, age, weight, the types of disease or disorder, stage of the disorder, the percentage of the desired cells in the cell population and the amount of cells needed to produce a therapeutic benefit. In one particular embodiment, the composition is administered by intravenous infusion and comprises at least about 110.sup.4 cells/kg or at least about 110.sup.5 cells/kg, for example from about 110.sup.4 cells/kg to about 110.sup.8 cells/kg or from about 110.sup.4 cells/kg to about 110.sup.7 cells/kg.
(98) The subjects that may be treated using the methods described herein are mammals, including, but not limited to, cows, sheep, goats, horses, dogs, cats, guinea pigs, rats, monkeys or other bovine, ovine, equine, canine, feline, rodent or murine species, primates, and preferably a human being, male or female.
(99) Other applications of the methods described herein Include, for example, preservation of tissues, grafts (e.g., vascular grafts) and ex vivo organ perfusions (e.g. lung perfusion (EVLP)).
MODE(S) FOR CARRYING OUT THE INVENTION
(100) The present invention is illustrated in further details by the following non-limiting examples.
Example 1: HSP90-Cochaperone Inhibitors as Cell Conditioning Agents
(101) In an attempt to identify conditioning compounds that are able to ensure in vivo cellular viability, based on preliminary evidence using Celastrol, over a dozen compounds with structural similarities identified through literature and the Sigma-Aldrich Structure Search online tool, were screened. The compounds' capacity to improve viability of human MSCs challenged to hypoxic stress was measured. The molecules that were screened, most of which are natural compounds, can be classified as triterpenoids, limonoids, with anolides, sterols, isoprenoides/diterpenes and flavonoids. Classical HSP90 inhibitors were also added to the screen, such as Radicicol that directly target the ATP binding pocket at the NT region of HSP90.sup.9 (NT inhibitor). The screens have shown variable efficacy of compounds in enhancing viability of cells during hypoxic stress (
Example 2: Celastrol Enhances Transplanted Cell Retention In Vivo and Enhances Paracrine Secretion
(102) The results described below show that Celastrol Increases in vivo viability and retention of transplanted cells. Briefly, rat MSCs were treated in suspension with conditioning compounds for 60 minutes. Cells were then washed, labeled with fluorescent cell tracker and injected at t=0 in rat left ischemic hindlimb. Transplanted cells were imaged in vivo until day 9 using Optix MX3 Molecular Imaging System from ART (
(103) Briefly, rat MSCs were incubated with low serum media (MEM 1X, 1% (Fetal Bovine Serum (FBS), 1% Penicillin-Streptomycin (P-S)) containing either Celastrol (10E-6M-10E-8M) or Vehicle (Dimethyl sulfoxide (DMSO)) for one hour. The media is then aspirated, cells are washed with 3 changes of media (MEM 1X, 1% FBS, 1% P-S). Cells are trypsinated and stained with Vybrant CFDA (Thermo Fisher Scientific) according to the manufacturer's protocol that allows detection in fluorescent imaging (Optix MX2). Cells are then counted using the Countess II FL automated cell counter (Thermo Fisher Scientific) and 3 million viable MSC'c are injected in the ischemic rat hindlimb model, using a 26G needle and syringe at 5 different points in 200 ul total volume.
(104) Sprague-Dawley rats (CD CRL: Charles River) are anesthetized (isoflurane 2.5-3.0% (Abbott Laboratories, Abbott Park, IL), 1 L/min oxygen) and bupivicaine is injected into the thigh (2 mg/kg sc qd) at the site of the Incision. The left common femoral artery Is cleared and the distal portion of the saphenous artery and all collateral branches and veins are dissected. The proximal and distal portion of the artery between the inguinal ligament and the knee is excised. Thus, none of the branches of the femoral artery can form collaterals. The lower right limb of each animal Is kept Intact and serves as a control. The wound Is closed using Vicryl 5-0. The animal receives buprenorphine hydrochloride (0.05 mg/kg s.c. bid 3 days) and is placed in its cage on Diamond soft litter. The day after the surgical procedure, PBS or MSCs pretreated with the vehicle or experimental compound are injected. The animals are anesthetized (isoflurane 2.5-3.0% (Abbott Laboratories, Abbott Park, IL), 1 L/min oxygen) and the cells are Injected directly into the quadriceps with a 26G needle and syringe at 5 different points.
(105) Transplanted cells were imaged in vivo until day 9 using Optix MX3 Molecular Imaging System from ART and in parallel, rats undergo Doppler scanning (Moor instruments) of the hindlimb which allows to study the recovery of the blood flow (below the knee) in a model of ischemia of the lower rat limb (n=3) after transplantation of conditioned rMSC.
(106) Celastrol conditioned cells increase viability and retention of stem cells implanted in the rat Ischemic hindlimb and ameliorate compared to vehicle treated cells the progressive recovery (as seen in a logarithmic pattern) the blood flow in the affected limb.
Example 3: Identification of Stem Cell Pharmaco-Optimizers
(107) Criteria for Identifying Stem Cell Pharmaco-Optimizers
(108) The criteria for identifying stem cell pharmaco-optimizers rely on the ability of the treatment to preferably satisfy two main conditions: 1. Treatment of cells would preferably confer an Increased in vivo viability and retention profile especially in the context of stem cell transplantation in hypoxic and/or oxidative microenvironments as observed in ischemic tissues; and 2. Treatment of cells would preferably allow maintenance of normal cellular phenotype and/or functionality as much as possible. However, highly desirable pharmaco-optimizers may also enhance cellular functions to promote a beneficial or therapeutic phenotype. In the case of stem cells, tissue repair involving paracrine activities, the pharmaco-optimizers may preferably enhance secretion of beneficial proteins and/or reduce production of deleterious proteins, thereby having a favourable balance and Impact on the transplant environment.
Methods to Test Candidate Stem Cell Pharmaco-Optimizers
(109) To test the first main condition, MSCs (either sourced from rat or humans) were treated with the candidate pharmaco-optimizers, washed and submitted to hypoxia/serum starvation (<1% O.sub.2 in hypoxia chamber in low serum media for 48-72 hours) or oxidative stress (incubation in media for 1 hour spiked with 0-2 mM H.sub.2O.sub.2), which mimic the major lethal stressors present in the ischemic transplant microenvironment. Viability status of cells are assessed using the LIVE/DEAD viability/cytotoxicity kit (Life Technologies) and results are quantified by Operetta high content screening (HCS) apparatus equipped with Harmony automated analysis software (Perkin Elmer).
(110) To test the second main condition, MSCs were treated with the candidate pharmaco-optimizers for 1 hour, followed by 3 hours washout period. Cell mRNA was extracted and expression of genes of interest was quantified by real time PCR. In additional MSC cultures, cells were treated for one hour, washed and cultured in low serum media for 24 hours. The media containing paracrine factors secreted by MSCs was then placed in contact with H9c2 cardiomyoblast cell line. H9c2 cells were then submitted to the hypoxia/serum starvation (<1% O.sub.2 in hypoxia chamber in low serum media for 48 hours) or oxidative stress (incubation in media for 1 hour spiked with 0-1 mM H.sub.2O.sub.2). Viability status of H9c2 cells was evaluated using the LIVE/DEAD assay as detailed above.
(111) In order to identify the mechanisms responsible for the protection of conditioned MSC and for the protection afforded to H9c2 via paracrine mechanism when incubated with conditioned MSC media, various molecules were selected as conditioning agents targeting two major cellular pathways, namely the heat shock pathway through HSP90 targeting (HSF1 activation) and/or the Nuclear factor (erythroid-derived 2)-like 2 (NRF2) pathway.
(112) Tested compounds (
(113) The results of these experiments, which are reported in
(114) Taken together, these results demonstrate that an optimal pharmaco-conditioning treatment for enhancement of cell viability combines the activity of an HSP90 co-factor inhibitor capable of HSF1 induction (resilience to hypoxia-induced death through direct and paracrine effect) and of an antioxidant NRF2 pathway inducer (resilience to oxidative stress-induced death through direct and paracrine effect). It was discovered that EGCG enhances Celastrol-stimulated cell protection.
(115) In addition to viability enhancement (first criteria for stem cell pharmaco-optimizer selection), the enhancement of the expression profile (second criteria for stem cell pharmaco-optimizer selection) through quantification of mRNA expression of HSPs, growth factors (GF), antioxidant proteins/enzymes and cytokines Implicated in inflammation was assessed. Mono and combination treatments were tested.
(116) Combination Treatments TestedFirst Experiment:
(117) Celastrol (1 M) or Gedunin (1 M)+EGCG (1 M, 10 M) or TBHQ (1 M, 5 M)
(118) The results of these experiments, which are reported in
(119) Expression of HSPs
(120) EGCG and tBHQ produce synergistic increase of Celastrol-induced HSP70 and HSP32 expression (
Expression of Growth Factors (GFs) EGCG synergistically enhances Celastrol stimulated expression of FGF2 and VEGF, whereas TBHQ increases and decreases both Celastrol and Gedunin expressions of FGF2 and VEGF respectively (
Expression of Antioxidant Factors EGCG synergistically enhances Celastrol stimulated expression of CAT, GPx, GR and SOD1 (
Expression of Inflammatory Cytokines. Celastrol and Gedunin downregulate IL1induced expression by EGCG and tBHQ (
(121) Together, these results show that EGCG synergistically potentiates Celastrol-stimulated expressions of favourable factors for stem cell function. Without wishing to be bound by theory, this may be due to the inhibition by EGCG of an unknown Celastrol functionality repressor or stabilization of HSP90 conformation for enhanced Celastrol effect. It cannot be excluded that the synergistic effect may also be secondary at least in part to activation of an NRF2 mediator and/or normalisation of the cell redox balance. Indeed, tBHQ, which has no HSP90 inhibiting activity, shows certain synergistic or additive effects on Celastrol stimulated expression in at least one rat line of MSCs. Finally. EGCG and tBHQ co-treatments with Celastrol or Gedunin further downregulate inflammatory cytokines.
(122) A compilation of the viability and expression results is presented in
(123) Interestingly, the Applicant found that, 2HBA, tBHQ and EGCG also produce synergistic increase when combined with Celastrol in increasing the viability of H9c2 cardiomyoblasts challenged by an oxidative stress (incubation in 1 mM H.sub.2O.sub.2 for 1 hour) (
Example 4: Identification of Celastrol Analogs as Stem Cell Pharmaco-Optimizers
(124) Using a similar approach to that described in Example 3, the Applicant tested several Celastrol analogs including those exemplified in
(125) The Applicant also tested several combination treatment of Celastrol or Celastrol analogs with potential adjunct agents (e.g., NRF-2 activators and/or antioxidants,
(126) In addition, 1-hour treatment of human mesenchymal stem cells (hMSC) with Celastrol combined with 2HBA, EGCG, tBHQ or Curcumin produce additive to synergistic increase in VEGF protein after 48 hours in normal culture whereas culturing the same cells for 48 hours in hypoxic condition as encountered in an infarct microenvironment produces even greater expression of VEGF protein (
Example 5: Celastrol Increases rMSC Viability Following Cryopreservation
(127) Proper cryopreservation is an important aspect for cell processing labs which are required to demonstrate that their cryopreservation protocol results in acceptable post-thaw viability (70%) before transplant. For example, studies have demonstrated that cryopreservation induces significant alterations of thawed hepatocytes and impairs their viability, attachment and function. The results presented in
(128) Mesenchymal stem cells (MSC) are Isolated from male rats (175-200 g) hindlimb bone marrow, and expanded as described. Briefly, bone marrow mononuclear cells (BMNCs) are isolated by Ficoll-Paque (Amersham) gradient centrifugation and cultured in Minimum Essential Medium alpha 1X (MEM 1X: Gibco 12571) with 10% FBS (Gibco) and 1% penicillin-streptomycin (P-S: Invitrogen 15140). After 48 h, nonadherent cells are discarded, and cells are washed with new medium. MSC are separated from hematopoletic cells based on preferential attachment to polystyrene surface. Multilineage potential of MSC is confirmed by in vitro adipogenic and osteogenic/chondrogenic differentiation assays with specific culture conditions and staining. Immunophenotyping is performed by multiparameter flow cytometry (FACScan; Becton Dickinson; Mountain View, CA, USA) with monoclonal antibodies directed against surface antigens such as CD29, CD34, CD45, CD90, CD105 (Coulter Immunology, Hialeah, FL, USA). For in vitro experiments, MSC will be used between 4.sup.th and 10.sup.th passage.
(129) Cell Viability Protocol (Freeze/Thaw Cycle)
(130) MSC are resuspended in 10% serum media (MEM 1X, 10% FBS, 1% P-S) and plated using a multichannel pipette in 96 well plates at a density of 4000 cells per well and incubated at 37 C. Each experimental and control conditions are plated in triplicate. The next day, the media is gently aspirated and replaced with low serum media (MEM 1X, 1% FBS, 1% P-S) containing either Celastrol (10E-6M) or Vehicle (DMSO) for one hour. The media is then aspirated, cells are washed with 3 changes of media (MEM 1X, 1% FBS, 1% P-S). Cells are trypsinated and counted using the Countess II FL automated cell counter (Thermo Fisher Scientific).
(131) Freezing cells: Following trypsination and counting steps as described above, cells are aliquoted at the desired density, DMSO is added (1:10 final dilution) to the cellular concentrate and transferred to pre-labelled cryovials. Cryovials are placed in freezing container and transfer to 80 C. overnight, and later transferred to 150 C.
(132) Thawing cells: Frozen cells are rewarmed by pouring pre-warmed culture medium on top of the frozen aliquot. Vials are centrifuged (200g; 3 min), supernatant is aspirated and cells are re-suspend in pre-warmed 10% serum media (MEM 1X, 10% FBS, 1% P-S). Trypan blue dilution is added to a cell aliquot and viability is measured using the Countess II FL automated cell counter (Thermo Fisher Scientific).
Example 6: Celastrol Increases Resistance to Oxidative Stress Induced Death In Vivo
(133) The results presented in
(134) Mesenchymal stem cells (MSC) are isolated as described in Example 5.
(135) In Vivo Conditioning
(136) Sprague-Dawley rats (CD CRL; Charles-River) receives 1 or 2 intraperitoneal injections of Celastrol (1 mg/kg) or Vehicle at 12 hours interval. Rats were then sacrificed and MSC were isolated as described above. MSC were placed in culture by resuspending in 10% serum media (MEM 1X, 10% FBS, 1% P-S) and plated using a multichannel pipette in 96 well plates at a density of 4000 cells per well and incubated at 37 C. Each experimental and control conditions are plated in triplicate.
(137) Cells are then challenged by incubation with 1% serum media containing 0 mM, 0.5 mM, 0.75 mM, or 1 mM hydrogen peroxide (ACP Chemicals, H7000) for 60 minutes. Cells are then gently washed twice with warm MEM 1X media stained with the LIVE/DEAD kit (Thermo Fischer Scientific) according to the manufacturer's protocol. Images are captured and analysed using a High content screening (HCS) system Operetta, running Harmony High-Content Imaging and Analysis software ver. 4.1 (Perkin Elmer, Waltham, MA). The results presented herein show that in vivo treatment of Sprague-Dawley rats with either one or two Injections of Celastrol, dose-dependently conditions bone marrow cells to withstand oxidative stress induced death.
Example 7: Celastrol Preserves Endothelial Layer Viability
(138) Pig carotid artery was harvested, dissected into closed rings and semi-circles open rings structures and placed overnight in Hank's Balanced Salt Solution (HBSS) or HBSS containing Celastrol at 10E-6M final concentration. Carotid rings were stained with the LIVE/DEAD kit (Thermo Fischer Scientific) according to the manufacturer's protocol. Tissues were imaged by confocal microscopy (Olympus, FV1000MPE/BK61WF) with 20X dipping objective. Z-stacks of carotid endothelial surface were also obtained.
Example 8: Celastrol Induces Cytoprotective Mediators
(139) Celastrol Induces cytoprotective mediators (survival kinases: pAkt/Akt, pERK/ERK; antioxidant HO1; Heat shock response proteins: HSF1, HSP70) and protein expression kinetics similarly in various cell types (times tested 5 to 120 min treatments for 10.sup.4M dose and either 0 to 24 hour recuperation following 1 hour treatment with 10.sup.4M Celastrol).
(140) More particularly INS-1 cells were cultured. In complete media (RPMI supplemented with filtered solutions: 1 mM Na pyruvate+50 M b mercaptoethanol, 10 mM Hepes Ultra pure, 2 mM L-Glutamine) containing 10% FBS. Cells are trypsinated (0.25% Trypsin-EDTA), centrifuged at 1500 RPM for 5 minutes and resuspended in complete INS media supplemented with 1% FBS. Cells are counted using a hemacytometer and 1-2 million cells are resuspended in Sarstedt tubes containing 9 mls of 1% FBS complete INS media and 2.5 ul or 5.0 ul of 1 mM Hsp90 inhibitor (Celastrol: Cayman Chemical 70950, Geldanamycin: Cayman Chemical 13355, or Radicicol: Cayman Chemical 13089) resuspended. In DMSO. Control samples are prepared similarly but by replacing Hsp90 inhibitor with either 2.5 ul or 5.0 ul of DMSO vehicle. The volume of cell suspensions are completed to a final volume of 10 ml with 1% FBS complete INS media. Suspensions are gently mixed by a few inversions and tubes are placed at 37 C for 30 minutes. Inversions are repeated after 15 minutes. Tubes are then centrifuged at 1500 RPM for 5 minutes, the media is gently aspirated, and the cells are washed with 12 mls of warm RPMI solution. The spin and wash cycle Is repeated twice more before resuspending cells with 2.5 ml or 5.0 ml of complete INS media containing 1% FBS, for the pellets containing 1 or 2 million cells respectively. Next, using a multichannel pipette, 100 ul aliquots of cell suspension containing 40,000 cells each are plated in 96 well plates. Each experimental and control conditions are plated. In quadruple and Incubated. In normoxic or hypoxic condition for 6 hours. Hypoxia (<1% oxygen) Is achieved by placing culture plates in an air tight hypoxia chamber (Billups-Rothenberg) and flushed for 10 minutes at a flow rate of 15-20 liters per min with a gas mixture of 5% CO.sub.2 balanced with 95% N.sub.2. After 6 hours of incubation, media from hypoxia-challenged and normoxic control cultures is replaced with 90 ul of 10% FBS complete INS media, and 10 ul of PrestoBlue reagent is added to each well. After 60 minutes of incubation, viability is quantified by fluorescence acquisition using a plate reader.
(141) These data show that short preconditioning of INS-1 cells with Celastrol protects cell viability when challenged by lethal hypoxic stress (
Example 9: Celastrol Rescue Rats from Lethal Drop in Blood Pressure Induced by LPS
(142) In addition to the effect of Celastrol in decreasing infarct size and the preservation of cardiac function in rats, the Applicant observed a modulation of blood pressure. In treated rats. Considering the potential of the compounds and combinations described herein in the preservation of organs and tissues to damage (i.e., ischemic, oxidative, inflammatory, necrotic) and in the preservation of systemic pressure/perfusion, their use in shock models (i.e. septic, cardiogenic) would be desirable in view of the high rates of organ failure and mortality associated with these conditions. Indeed, in the United States, more than 750,000 annual cases of severe septicemia are diagnosed with a mortality rate of 25-30% (Crit Care Med 29 (7): 1303Y1310, 2001). caused by failure of multiple organs including cardiac dysfunction as a critical manifestation (Circulation 116 (7): 793Y802, 2007). We propose the addition of a septic shock model either the endotoxic model induced by the bacterial lipopolysaccharide (LPS) in the rat (Life Sci., 1997; 60 (15): 1223-30).
(143) Briefly SD rats are anesthetized with isoflurane 2.5-3.0% (Abbott Laboratories, Abbott Park, IL), 1 L/min oxygen and placed on a heated blanket to prevent hypothermia. The left external carotid artery is cannulated with gelco #20 and relayed to a pressure sensor. Alternatively, depending on the size, the left femoral artery is cannulated. The rats are kept at 2% isoflurane, 1 L/min oxygen, and basal pressure measurements are collected. The pressure kinetics in response to i.v. injection via the jugular vein of LPS (20 to 50 mg/Kg) and injection I.p. of Celastrol (1 mg/Kg) is determined. It is noteworthy to mention that the dose of LPS in animals may be variable and also depend on the age of the animals (Infection and immunity, March 1996, Vol. 64, no. 3, p769). In our experiment, both rats received a first bolus of LPS at 10 mg/kg. Following transient drop in blood pressure (BP) for both rats, BP stabilized and regained baseline value. Then either an injection of a bolus of 300 ul i.p. of Celastrol (1 mg/Kg) or vehicle (10% DMSO, 70% Cremophor EL/ethanol (3:1). 20% PBS) was performed in distinct rats (see arrow;
Example 10: Celastrol Induces the Expression of Hsp32 (HO-1) in the Kidney of Rats
(144) The Applicant previously showed that Celastrol promoted cardiomyocyte survival, reduction of injury and adverse remodelling with preservation of cardiac function in the rat ischemic myocardium. The Applicant tested whether this protective effect could be observed in other types of Ischemic diseases.
(145) Rats are anaesthetized with 2.0%-3.0% isoflurane (Abbott Laboratories) in 1 L/min of oxygen, and placed in supine position on a heating pad. Rats receive a single bolus injection of Vehicle solution or Celastrol ((Cayman Chemical 70950) 50 mM stock solution resuspended in 0.2 uM filter sterilized vehicle: DMSO (Sigma 154938) (4% total volume), PBS 1X (96% total volume)) via the external jugular vein at a dose of 1 mg/kg. Rats are shaved, ophthalmic ointment is applied to corneas, and bupivacaine (2 mg/kg s.c.) Is injected at the site of the 3-4 cm incision starting at the base of the sternum to the ombilic. The incision is maintained open with retractors, and the intestines are wrapped in sterile saline damped gauze. The left kidney (K) is isolated and the renal artery is occluded with a vascular clip. The intestines are replaced in the abdominal cavity and the skin is closed with temporary 3-0 sutures (Ethicon). Rats receive buprenorphine hydrochloride (0.05 mg/kg s.c.) and are maintained with 1.0%-2.0% isoflurane (Abbott Laboratories) in 1 L/min of oxygen for 30 minutes of ischemia and an additional 45 minutes of reperfusion following removal of the clip. Rats are exsanguinated by perfusion with 40 mM KCl supplemented saline and organs are harvested, rinsed in cold phosphate buffered saline (PBS1X), preserved in 10% formalin buffered with PBS overnight for paraffin embedded for histological/immunohistological sections or snap frozen in liquid nitrogen for western blot expression analysis.
(146) Results of the Western Blot analysis presented herein demonstrate that a single injection of Celastrol (1 mg/kg) induces the expression of Hsp32 (HO-1) within 60 minutes in the kidney of rats (
Example 11: Effect of Celastrol and Celastrol Analogs on Cell Viability and Protection from Stress and Damage
(147) The Applicant tested the effect of Celastrol or Celastrol analogs on hypoxic cultures of H9c2 rat cardiomyoblasts and in a rat model of myocardial infarction. The combinations of Celastrol or Celastrol analogs with adjunct agents may tested in a similar fashion.
(148) In Vitro Studies
(149) Cell Culture and Stimulation:
(150) For survival to hypoxic challenge and oxidative challenge, H9c2 cardiomyoblasts are submitted to the hypoxia/serum starvation (<1% O.sub.2 in hypoxia chamber in low serum media for 48 hours) or oxidative stress (incubation in media for 1 hour spiked with 0-1 mM H.sub.2O.sub.2). Viability status of H9c2 cells was evaluated using the LIVE/DEAD assay.
(151) Next, the hypoxia/reoxygenation challenge is performed. Briefly, viability analysis was performed in rat H9c2 cardiomyoblasts as previously reported. For hypoxia/reoxygenation stress, cells were cultured in DMEM no glucose (Life Technologies), serum starved and placed. In hypoxic conditions (<1% O.sub.2) for 18 h. At reoxygenation (normoxic conditions), cells were treated with Celastrol (10.sup.10 to 10.sup.6 mol/L, Cayman Chemical, Ann Arbor, MI), Celastrol analogs or vehicle (Dimethyl sulfoxide (DMSO), Sigma-Aldrich Canada, Oakville, ON; final concentration <1% v/v) in DMEM high glucose 1% FBS for 1 h, then reoxygenation was continued in DMEM high glucose for an additional 5 h.
(152) The results presented in
Example 12: Celastrol and Celastrol Analogs for Use in Treatment of Ischemic Disease
(153) Lewis rats (250-300 g, Charles River, St Constant, QC) were used in all ex vivo and in vivo experiments. All animals were handled according to the Guide for the Care and Use of Laboratory Animals.
(154) Ex Vivo Studies
(155) Isolated Perfused Heart Preparation:
(156) Rats were randomly assigned to the following groups: Vehicle (n=6), Celastrol or Celastrol analogs 10.sup.8, 10.sup.7 or 10.sup.6 mol/L (n=5 each). Under isoflurane anesthesia rats were injected with Heparin (I.P, 1000 I.U, Novartis, Dorval, QC) and hearts were harvested and immediately submerged in ice cold Krebs buffer (in mmol/l: NaCl 113, KCl 4.5, NaH.sub.2PO.sub.4 1.6, CaCl.sub.2 1.25, MgCl.sub.2+6H.sub.2O 1, D-Glucose 5.5, NaHCO.sub.3 25). The heart was retrogradely perfused using a Langendorff system (Radnoti, Monrovia, CA) with a constant aortic pressure of 60-70 mmHg, using Krebs buffer at 37 C., bubbled with 5% CO.sub.2 balanced O.sub.2. A latex balloon connected to a pressure transducer was Inserted in to the left ventricle (LV) and adjusted to 15 mmHg (LV preload). Hearts were paced at 300 bpm and allowed 20 minutes of stabilization.
(157) Intraventricular pressures were continuously measured using a Power lab 8/30 polygraph (ADinstruments, Colorado Springs, CO), recorded and analysed using LabChart pro v.7.3.7 (ADinstruments).
(158) To ensure that Celastrol, Celastrol analogs or vehicle (DMSO) were in contact with the heart at the moment of the initiation of reperfusion, the system was primed at the moment of inducing warm global Ischemia, achieved by stopping cardiac pace and perfusion for 30 minutes. Reperfusion was started using Krebs buffer with Celastrol (10.sup.8, 10.sup.7 or 10.sup.6 mol/L) or vehicle for 10 minutes, then continued (Krebs buffer) for a total reperfusion time of 120 minutes.
(159) Cardiac effluent was collected for 5 minutes at the end of stabilization, at 5 minutes reperfusion and then every 15 minutes for 60 minutes in total. Volumes were measured and samples kept at 80 C. until analysis.
(160) At the end of reperfuslon, hearts were sliced transversally (1-2 mm), and stained with 5% 2,3,5-Triphenyl-tetrazolium chloride in phosphate buffer saline pH 7.4 (TTC, Sigma-Aldrich Canada) for 20 min at 37 C..sup.15. Slices were weighed, then images were taken using a Stemi 508 Stereo microscope coupled to a AxioCam ERc 5s camera and processed with Zen 2.3 imaging software (Carl Zeiss Canada, Toronto, ON). Analyses were performed using ImageJ 1.51 h freeware (NIH, Bethesda, MD). Infarct area was normalised to the weight of the heart tissue slice. One slice per heart was snap frozen for gene and protein expression.
(161) The results presented in
(162) In Vivo Studies
(163) Rats were randomly assigned to the following groups: Sham (n=6), Vehicle (n=8), Celastrol 1 mg/Kg (n=6) or Celastrol analogs. Under 2% isoflurane anesthesia, baseline echocardiography using a Sonos 5500 Imaging System (Philips, Philips Healthcare, Andover, MA, USA) with a 12 MHz transducer was performed as described.sup.12. All measures were acquired by the same experienced observer, blinded to the treatment. For each measurement, three to five cardiac cycles were analysed and averaged.
(164) After echocardiography, the animal was intubated and mechanically ventilated, then bupivacaine 2 mg/kg was injected, and a left thoracotomy was performed, exposing the heart. Using a 5-0 silk slipknot, an occlusion of the left anterior descending coronary artery was performed. Visual blanching and electrocardiographic changes confirmed myocardial ischemia. In Sham animals, suture was not ligated. After 30 minutes, the suture occlusion was released. Celastrol, Celastrol analogs or vehicle was injected intraventricularly for acute systemic delivery, then the chest was closed. Buprenorfine (0.05 mg/Kg sc) and carprofen (5 mg/Kg sc) were Injected at the end of surgery. Animals were left to recuperate for 24 h, then a second echocardiography was performed. Animals were sacrificed, cardiac tissue was snap frozen, and blood was collected in heparinized tubes, then centrifuged at 4 C. Plasma was collected, snap frozen and kept at 80 C. until analysis.
(165) Results of
(166) Statistical Analyses
(167) Data are expressed as mean t standard error or median with 95% confidence interval. ANOVA test was used for group comparison of non-repeated measurements. For repeated measurements, linear mixed-effect models were used to compare groups (MIXED procedures in SAS software, version 9.3; SAS Institute, Cary, NC, USA). Between-group differences were assessed. For non-normally distributed measurements, such as indexes and ratios, a log transformation of the measurements was used. For hemodynamic measurements, as much as 200 measurement per rats per time points were used in the model, with each single measurement weighted accordingly (i.e. 1/200). For all analyses. P<0.05 was considered statistically significant.
Example 13: Celastrol and Celastrol analogs modulate expression of genes under the control of HSR and ARE elements
(168) H9c2 rat cardiomyoblasts were seeded at a density of 5,000 cells per well in 96 well plates in DMEM 10% FBS complete medium and transfected using lipofectamine with the Cignal Reporter Assay Heat shock response and Antioxidant response kits (SABiosciences, Qiagen) according to the manufacturers' protocol. The next day, Celastrol, analogs and various other compounds were added to the wells in triplicate at a dose range of 10E-5 to 10E-10M in DMEM 1% FBS media for 4 hours followed by 3 hours of washout period complete media prior to measuring the signaling activity using the Dual Luciferase Assay (Promega) The results summarized in
(169) Although the present invention has been described hereinabove by way of specific embodiments thereof, it can be modified, without departing from the spirit and nature of the subject Invention as defined in the appended claims. In the claims, the word comprising is used as an open-ended term, substantially equivalent to the phrase including, but not limited to. The singular forms a, an and the include corresponding plural references unless the context clearly dictates otherwise.