PHARMACEUTICAL COMPOSITION FOR PREVENTING OR TREATING FABRY DISEASE, CONTAINING TSP1 PROTEIN INHIBITOR AS ACTIVE INGREDIENT
20220034908 · 2022-02-03
Inventors
Cpc classification
A61K31/7088
HUMAN NECESSITIES
A61K31/7088
HUMAN NECESSITIES
C12N15/90
CHEMISTRY; METALLURGY
A61K31/4439
HUMAN NECESSITIES
A61P43/00
HUMAN NECESSITIES
G01N2500/04
PHYSICS
A61K31/713
HUMAN NECESSITIES
A61K31/4439
HUMAN NECESSITIES
A61K2300/00
HUMAN NECESSITIES
A61K2300/00
HUMAN NECESSITIES
G01N2333/78
PHYSICS
International classification
Abstract
The present invention relates to a pharmaceutical composition for preventing or treating Fabry disease, containing a TSP1 protein inhibitor as an active ingredient. Particularly, in vascular endothelial cells produced by knocking out a TSP1 gene in induced pluripotent stem cells derived from a Fabry disease patient, of the present invention, the recovery of cell morphology, a decrease in the expression of a TSP1 gene, a decrease in the expression levels of a TSP1 protein and a phosphorylated-SMAD protein, which are anti-angiogenic factors, and an increase in the expression levels of a KDR protein and an eNOS protein, which are angiogenic factors, have been confirmed, and thus a TSP1 gene expression inhibitor or a TSP1 protein activity inhibitor can be effectively used in the treatment of Fabry disease.
Claims
1. A method for preventing or treating Fabry disease comprising administering a TSP1 (Thrombospondin1) gene expression inhibitor or a TSP1 protein activity inhibitor to a subject in need thereof.
2. The method for preventing or treating Fabry disease according to claim 1, wherein the TSP1 gene is a polynucleotide composed of the nucleotide sequence represented by SEQ. ID. NO: 1.
3. The method for preventing or treating Fabry disease according to claim 1, wherein the TSP1 gene expression inhibitor includes any one or more selected from the group consisting of antisense nucleotides, siRNA (small interfering RNA), shRNA (short hairpin RNA) and ribozyme against the polynucleotide constituting TSP1 gene.
4. The method for preventing or treating Fabry disease according to claim 1, wherein the TSP1 protein is a polypeptide composed of the amino acid sequence represented by SEQ. ID. NO: 2.
5. The method for preventing or treating Fabry disease according to claim 1, wherein the TSP1 protein activity inhibitor includes any one or more selected from the group consisting of compounds, peptides, peptide mimetics, matrix analogs, aptamers, and antibodies that complementarily bind to the polypeptide constituting TSP1 protein.
6. (canceled)
7. A screening method of a candidate therapeutic agent for Fabry disease comprising the following steps: 1) treating a test material to a cell line expressing TSP1 protein; 2) measuring the expression level of the TSP1 protein in the cell line; and 3) selecting a test material that has reduced the expression level of the TSP1 protein compared to the control not treated with the test material.
8. The screening method of a candidate therapeutic agent for Fabry disease according to claim 7, wherein the test material of step 1) is one or more substances selected from the group consisting of peptides, proteins, non-peptidic compounds, active compounds, fermentation products, cell extracts, plant extracts, animal tissue extracts and plasma.
9. The screening method of a candidate therapeutic agent for Fabry disease according to claim 7, wherein the protein expression level of step 2) is measured by any one or more methods selected from the group consisting of enzyme-linked immunosorbent assay (ELISA), radioimmunoassay, sandwich enzyme immunoassay, western blot, immunoprecipitation, immunohistochemistry, fluoroimmunoassay and flow cytometry (FACS).
10. A screening method of a candidate therapeutic agent for Fabry disease comprising the following steps: 1) treating a test material to TSP1 protein; 2) measuring the activity level of the TSP1 protein; and 3) selecting a test material that has reduced the activity level of the TSP1 protein compared to the control not treated with the test material.
11. The screening method of a candidate therapeutic agent for Fabry disease according to claim 10, wherein the protein activity level of step 2) is measured by any one or more methods selected from the group consisting of enzyme immunoassay, fluoroimmunoassay, SDS-PAGE, mass spectrometry and protein chip.
12. A protein detection method for providing information necessary for diagnosis of Fabry disease comprising the following steps: 1) measuring the expression level of TSP1 protein in the sample derived from a subject; and 2) determining the subject with the increased expression level of the TSP1 protein compared to the control group as a subject at risk of developing Fabry disease.
13. A method for preventing or treating Fabry disease comprising administering SB-431542 to a subject in need thereof.
14. The method for preventing or treating Fabry disease according to claim 13, wherein the SB-431542 is a compound represented by formula 1 below: ##STR00003##
15. The method for preventing or treating Fabry disease according to claim 13, wherein the SB-431542 reduces the expression of TSP1 protein in vascular endothelial cells of patients with Fabry disease.
16. The method for preventing or treating Fabry disease according to claim 13, wherein the SB-431542 increases the expressions of KDR (kinase insert domain receptor) and eNOS (endothelial Nitric oxide synthase) proteins in vascular endothelial cells of patients with Fabry disease.
17-18. (canceled)
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0077] Hereinafter, the present invention is described in detail.
[0078] The present invention provides a pharmaceutical composition comprising a TSP1 gene expression inhibitor or a TSP1 protein activity inhibitor as an active ingredient for preventing or treating Fabry disease.
[0079] The TSP1 gene can include all polynucleotides composed of any sequence known in the art, and can include a variant having one or more substitutions, insertions, deletions, and combinations thereof that do not reduce the activity. The variant can have 80%, 90%, 95%, 98% or more homology with the TSP1 gene sequence of the present invention. In an embodiment of the present invention, the TSP1 gene can be a polynucleotide composed of the nucleotide sequence represented by SEQ. ID. NO: 1. The TSP1 gene expression inhibitor can include any material known in the art as long as it suppresses mRNA of the gene encoding TSP1 protein, and can be prepared by various methods such as chemical synthesis or in vitro transcription synthesis. The expression inhibitor can include any one or more selected from the group consisting of antisense nucleotide, siRNA (small interfering RNA), shRNA (short hairpin RNA) and ribozyme complementarily binding to the polynucleotide constituting TSP1 gene.
[0080] The antisense nucleotide, as defined in the Watson-Crick base pair, refers to a sequence that interferes with the flow of genetic information from DNA to protein by binding (hybridizing) to the complementary nucleotide sequence of DNA, immature-mRNA or mature mRNA. In addition, since the antisense nucleotide is a long chain of monomer units, the antisense nucleotide for target RNA sequence can be easily synthesized.
[0081] The said siRNA refers to a short double-stranded RNA capable of inducing RNA interference through cleavage of specific mRNA. In addition, the siRNA is not limited to the region in which the double-stranded RNA is completely paired, and can include the region in which the strand is not paired due to mismatch (the corresponding nucleotide is not complementary) or bulge (no nucleotide corresponding to one chain). The siRNA terminal structure can have either a blunt end or a protruding end, as long as the expression of the target gene can be suppressed by the RNA interference effect, and the adhesive terminal structure can be both a 3′ end protruding structure and a 5′ end protruding structure.
[0082] The said shRNA refers to a sequence of RNA that makes a strong hairpin turn, which can be used to silence gene expression through RNA interference. In addition, the shRNA can be delivered to cells using a vector for cell introduction, and such vector is always delivered to daughter cells, so that gene silencing can be inherited. The shRNA hairpin structure is degraded into siRNA by an intracellular mechanism and bound to an RNA-induced silencing complex, and the complex binds to mRNA corresponding to the siRNA to degrade it.
[0083] The said ribozyme refers to an enzyme RNA molecule capable of catalyzing specific RNA cleavage. Endonucleolytic cleavage can be induced by the specific hybridization of the molecular sequence of ribozyme and the complementary target RNA. The ribozyme can include the known sequences responsible for the cleavage of one or more sequences complementary to the target RNA or the functionally equivalent sequences. In addition, the ribozyme can be a hammer-head ribozyme or a Cech type ribozyme, the endoribonuclease RNA, and can be formed by a modified oligonucleotide to improve safety and targeting. Meanwhile, the ribozyme can be distributed in cells expressing a target gene in vivo. DNA constructs encoding ribozyme under the control of a strong constitutive polymerase III or polymerase II promoter so that the transfected cells can destroy the endogenous target messenger and produce a sufficient amount of ribozyme to inhibit translation can be used. Since the ribozyme has a catalytic activity, it may have to be maintained at a low concentration in cells unlike other antisense molecules.
[0084] The said TSP1 protein can include a polypeptide composed of any sequence known in the art. The polypeptide can be a variant of amino acids having a different sequence by deletion, insertion, substitution or a combination thereof of amino acid residues, within a range that does not affect the function of the protein. Amino acid exchange in proteins or peptides that do not alter the activity of the molecule as a whole is known in the art. In some cases, it can be modified by phosphorylation, sulfation, acrylation, glycosylation, methylation, farnesylation, etc. The variant can have homology with at least 80%, 90%, or 95% with the TSP1 protein of the present invention. In an embodiment of the present invention, the TSP1 protein can be a polypeptide composed of the amino acid sequence represented by SEQ. ID. NO: 2.
[0085] The TSP1 protein activity inhibitor can include any one or more selected from the group consisting of compounds, peptides, peptide mimetics, matrix analogs, aptamers, and antibodies that complementarily bind to the polypeptide constituting the TSP1 protein.
[0086] The peptide and peptide mimetics can inhibit the TSP1 protein activity by suppressing the binding of the TSP1 protein to other proteins. The peptide mimetics can be a peptide or a non-peptide, and can be composed of the amino acids bound by a non-peptide bond such as a psi bond. Non-hydrolyzable peptide mimetics can be prepared using β-turn dipeptide core, keto-methylene pseudopeptides, azepine, benzodiazepine, β-amino alcohol or substituted gammalactam ring as a main residue.
[0087] The said aptamer refers to a single-stranded nucleic acid (DNA, RNA or modified nucleic acid) that has a stable tertiary structure by itself and can bind to a target molecule with high affinity and specificity. Since the aptamer can bind to organic matters, peptides, membrane proteins, etc., and block the function thereof, it can be regarded as a kind of a chemical antibody that replaces a single antibody. In addition, the aptamer can be obtained by separating oligomers that bind to specific chemical molecules or biological molecules with high affinity and selectivity using an oligonucleotide library called SELEX (systematic evolution of ligands by exponential enrichment).
[0088] The said antibody can be a monoclonal antibody, a polyclonal antibody, or a recombinant antibody. Antibodies against a specific protein can be easily prepared using the techniques well known in the art if the sequence of the protein is informed. Particularly, antibodies can be prepared using a hybridoma method or a phage antibody library technique. In general, hybridoma cells secreting monoclonal antibodies can be prepared by fusing immune cells isolated from immunologically suitable host animals such as mice injected with antigen proteins and cancer cell lines. The fusion of these two groups of cells can be performed using polyethylene glycol or the like, and the antibody-producing cells can be proliferated by standard culture methods. After a homogeneous cell population is obtained by subcloning using a limiting dilution method, hybridoma cells capable of producing antigen-specific antibodies can be prepared by mass-culture in vitro or in vivo. The antibodies prepared by the above methods can be separated and purified using the methods such as gel electrophoresis, dialysis, salt precipitation, ion exchange chromatography, and affinity chromatography, etc.
[0089] The polyclonal antibody can be prepared by injecting a biomarker protein or a fragment thereof as an immunogen into an external host. The external host can be mammals such as mice, rats, sheep, and rabbits. When the immunogen is injected by intramuscular, intraperitoneal or subcutaneous injection, it can be administered with an adjuvant for increasing antigenicity. Thereafter, blood is regularly collected from the external host to obtain serum showing improved titer and specificity to the antigen, and the antibody can be isolated and purified therefrom.
[0090] In a preferred embodiment of the present invention, the present inventors prepared induced pluripotent stem cells (FB-iPSCs) using cells of patients with Fabry disease, and confirmed the characteristics of the stem cells (
[0091] The present inventors also confirmed that vasculopathy was induced in vascular endothelial cells differentiated from FB-iPSCs by Gb3 protein (
[0092] In addition, the present inventors prepared an isotype control cell line of FB-iPSCs (
[0093] Therefore, the TSP1 gene expression inhibitor or the TSP1 protein activity inhibitor of the present invention can be effectively used for the prevention or treatment of Fabry disease.
[0094] The pharmaceutical composition can contain the TSP1 gene expression inhibitor or the TSP1 protein activity inhibitor of the present invention as an active ingredient at the concentration of 10 weight % by the total weight of the composition. In addition, the pharmaceutical composition of the present invention can contain, in addition to the active ingredient, one or more effective ingredients having the same or similar function to the active ingredient.
[0095] The pharmaceutical composition of the present invention can contain carriers, diluents, excipients, or combinations of at least two of those generally used in biological preparations. The pharmaceutically acceptable carrier can be any carrier that is able to deliver the composition of the present invention in a living body without limitation, which is exemplified by the compounds described in Merck index, 13th ed., Merck & Co. Inc., such as saline, sterilized water, Ringer's solution, buffered saline, dextrose solution, maltodextrin solution, glycerol, ethanol, and a mixture comprising one or more of those components. If necessary, a general additive such as antioxidant, buffer, and bacteriostatic agent can be additionally added.
[0096] When the composition is formulated, it is prepared using generally used diluents or excipients such as fillers, extenders, binders, wetting agents, disintegrating agents and surfactants.
[0097] The composition of the present invention can be formulated as an oral or parenteral formulation. Solid formulations for oral administration are tablets, pills, powders, granules and capsules. These solid formulations are prepared by mixing one or more compositions with one or more suitable excipients such as starch, calcium carbonate, sucrose, lactose and gelatin, etc. In addition, lubricants such as magnesium stearate and talc can be added thereto. Liquid formulations for oral administrations are suspensions, solutions, emulsions or syrups, and the above-mentioned formulations can contain various excipients such as wetting agents, sweeteners, aromatics and preservatives.
[0098] Formulations for parenteral administration are sterilized aqueous solutions, water-insoluble excipients, suspensions, and emulsions. Water insoluble excipients and suspensions can contain propylene glycol, polyethylene glycol, vegetable oil like olive oil, injectable ester like ethylolate, etc.
[0099] The composition of the present invention can be administered by orally or parenterally and the parenteral administration can be selected from the group consisting of skin external application or intraperitoneal injection, intrarectal injection, subcutaneous injection, intravenous injection, intramuscular injection, and intrathoracic injection.
[0100] The composition can be administered by the pharmaceutically effective amount. The effective amount can be determined according to the type of disease, the severity, the activity of the drug, the patient's sensitivity to the drug, the time of administration, the route of administration, the duration of treatment, the drugs being used simultaneously, and the like. The composition of the present invention can be administered alone or in combination with other therapeutic agents. In combination administration, the administration can be sequential or simultaneous. However, for the desired effect, the amount of the active ingredient included in the pharmaceutical composition according to the present invention can be 0.001˜10,000 mg/kg, specifically 0.1˜5 g/kg. The administration frequency can be once a day or a few times a day.
[0101] The present invention also provides a health functional food comprising a TSP1 gene expression inhibitor or a TSP1 protein activity inhibitor as an active ingredient for preventing or ameliorating Fabry disease.
[0102] The TSP1 gene and the TSP1 gene expression inhibitor can have the characteristics as described above. For example, the TSP1 gene can be a polynucleotide composed of the nucleotide sequence represented by SEQ. ID. NO: 1. In addition, the expression inhibitor can include any one or more selected from the group consisting of antisense nucleotide, siRNA, shRNA and ribozyme complementarily binding to the polynucleotide constituting TSP1 gene.
[0103] The TSP1 protein and the TSP1 protein activity inhibitor can have the characteristics as described above. For example, the TSP1 protein can be a polypeptide composed of the amino acid sequence represented by SEQ. ID. NO: 2. In addition, the activity inhibitor can include any one or more selected from the group consisting of compounds, peptides, peptide mimetics, matrix analogs, aptamers, and antibodies that complementarily bind to the polypeptide constituting the TSP1 protein.
[0104] In a preferred embodiment of the present invention, the present inventors prepared induced pluripotent stem cells (FB-iPSCs) using cells of patients with Fabry disease, and confirmed the characteristics of the stem cells (
[0105] The present inventors also confirmed that vasculopathy was induced in vascular endothelial cells differentiated from FB-iPSCs by Gb3 protein (FIGS. 17˜20), and SB431542, a TGF-β inhibitor, had an effect on the treatment of vasculopathy (
[0106] In addition, the present inventors prepared an isotype control cell line of FB-iPSCs (
[0107] Therefore, the TSP1 gene expression inhibitor or the TSP1 protein activity inhibitor of the present invention can be effectively used for the prevention or amelioration of Fabry disease.
[0108] The TSP1 gene expression inhibitor or the TSP1 protein activity inhibitor of the present invention can be used as a food additive. In that case, the TSP1 gene expression inhibitor or the TSP1 protein activity inhibitor of the present invention can be added as it is or as mixed with other food components according to the conventional method. The amount of the active ingredient can be regulated according to the purpose of use. In general, the active ingredient of the present invention is preferably added to the health functional food by 0.01˜90 weight part for the total weight of the food.
[0109] In addition, there is no particular limitation on the form and type of the health functional food. The form of the health functional food to which the above substances can be added may be tablets, capsules, powders, granules, liquids and pills.
[0110] The health functional food of the present invention can additionally include various flavors or natural carbohydrates, etc, like other conventional health foods. The natural carbohydrates above can be one of monosaccharides such as glucose and fructose, disaccharides such as maltose and sucrose, polysaccharides such as dextrin and cyclodextrin, and glucose alcohols such as xilytole, sorbitol and erythritol. Besides, natural sweetening agents such as thaumatin and stevia extract, and synthetic sweetening agents such as saccharin and aspartame can be included as a sweetening agent.
[0111] In addition to the ingredients mentioned above, the health functional food of the present invention can include in a variety of nutrients, vitamins, minerals, flavors, coloring agents, pectic acid and its salts, alginic acid and its salts, organic acid, protective colloidal viscosifiers, pH regulators, stabilizers, antiseptics, glycerin, alcohols, etc. All the mentioned ingredients can be added singly or together. The ratio of those ingredients can be selected in the range of 0.01˜0.1 weight part per 100 weight part of the composition of the present invention.
[0112] The present invention also provides a screening method of a candidate therapeutic agent for Fabry disease using a TSP1 protein.
[0113] The TSP1 protein can have the characteristics as described above. For example, the TSP1 protein can be a polypeptide composed of the amino acid sequence represented by SEQ. ID. NO: 2.
[0114] Specifically, the method can be composed of the following steps:
[0115] 1) treating a test material to a cell line expressing the TSP1 protein;
[0116] 2) measuring the expression level of the TSP1 protein in the cell line; and
[0117] 3) selecting a test material that has reduced the expression level of the TSP1 protein compared to the control not treated with the test material.
[0118] The test material of step 1) can be one or more substances selected from the group consisting of peptides, proteins, non-peptidic compounds, active compounds, fermentation products, cell extracts, plant extracts, animal tissue extracts and plasma.
[0119] The protein expression level of step 2) can be measured by any one or more methods selected from the group consisting of enzyme-linked immunosorbent assay (ELISA), radioimmunoassay, sandwich enzyme immunoassay, western blot, immunoprecipitation, immunohistochemistry, fluoroimmunoassay and flow cytometry (FACS).
[0120] Another method can be composed of the following steps:
[0121] 1) treating a test material to the TSP1 protein;
[0122] 2) measuring the activity level of the TSP1 protein; and
[0123] 3) selecting a test material that has reduced the activity level of the TSP1 protein compared to the control not treated with the test material.
[0124] The test material of step 1) can be one or more substances selected from the group consisting of peptides, proteins, non-peptidic compounds, active compounds, fermentation products, cell extracts, plant extracts, animal tissue extracts and plasma.
[0125] The protein activity level of step 2) can be measured by any one or more methods selected from the group consisting of enzyme immunoassay, fluoroimmunoassay, SDS-PAGE, mass spectrometry and protein chip.
[0126] In a preferred embodiment of the present invention, the present inventors confirmed the increase of the expression level of TSP1 protein in vascular endothelial cells differentiated from FB-iPSCs derived from patients with Fabry disease (
[0127] The present invention also provides a protein detection method for providing information necessary for diagnosis of Fabry disease using a TSP1 protein.
[0128] The TSP1 protein can have the characteristics as described above. For example, the TSP1 protein can be a polypeptide composed of the amino acid sequence represented by SEQ. ID. NO: 2.
[0129] Specifically, the method can be composed of the following steps:
[0130] 1) measuring the expression level of the TSP1 protein in the sample derived from a subject; and
[0131] 2) determining the subject with the increased expression level of the TSP1 protein compared to the control group as a subject at risk of developing Fabry disease.
[0132] In a preferred embodiment of the present invention, the present inventors confirmed the increase of the expression level of TSP1 protein in vascular endothelial cells differentiated from FB-iPSCs derived from patients with Fabry disease (
[0133] The present invention also provides a pharmaceutical composition comprising SB-431542, a TGF-β signaling pathway inhibitor, as an active ingredient for preventing or treating Fabry disease.
[0134] The “TGF (transforming growth factor) beta signaling pathway inhibitor” means a substance that inhibits signaling mediated by TGF beta. The TGF beta is a protein that regulates various physiological processes such as cell proliferation, differentiation, apoptosis, migration, extracellular matrix (ECM) production, angiogenesis, and development in vivo.
[0135] The TGF beta signaling pathway inhibitor can be SB-431542, but any substance capable of inhibiting TGF signaling can be used without limitation. In the present invention, SB431542 was used as the TGF beta signaling pathway inhibitor, and it can be represented by formula 1 below.
##STR00001##
[0136] The said SB-431542 can reduce the expression of TSP1 protein in vascular endothelial cells of patients with Fabry disease, and can increase the expressions of KDR (kinase insert domain receptor) and eNOS (endothelial Nitric oxide synthase) proteins.
[0137] In a preferred embodiment of the present invention, the present inventors confirmed that vasculopathy was induced in vascular endothelial cells differentiated from FB-iPSCs by Gb3 protein (
[0138] The pharmaceutical composition can have the characteristics as described above.
[0139] In addition, the present invention provides a health functional food comprising SB-431542, a TGF-β signaling pathway inhibitor, as an active ingredient for preventing or ameliorating Fabry disease.
[0140] The TGF-β signaling pathway inhibitor or SB-431542 can have the characteristics as described above. For example, the SB-431542 can have the structure of formula 1 below, can reduce the expression of TSP1 protein in vascular endothelial cells of patients with Fabry disease, and can increase the expressions of KDR and eNOS proteins.
##STR00002##
[0141] In a preferred embodiment of the present invention, the present inventors confirmed that vasculopathy was induced in vascular endothelial cells differentiated from FB-iPSCs by Gb3 protein (
[0142] The health functional food can have the characteristics as described above.
[0143] Hereinafter, the present invention will be described in detail by the following examples.
[0144] However, the following examples are only for illustrating the present invention, and the contents of the present invention are not limited thereto.
Example 1: Preparation of Induced Pluripotent Stem Cells (iPSCs) Derived from Patients with Fabry Disease
[0145] For the study of Fabry disease, fibroblasts were isolated from patients with Fabry disease, and iPSCs were induced in the following manner.
[0146] Particularly, with the consent of patients with Fabry disease at Asan Medical Center (Seoul, Korea), the patients were subjected to local anesthesia, and then the dermal tissue was obtained by performing skin tissue biopsy using punch biopsy. Clinical information of 4 patients with Fabry disease is shown in Table 1 below. All the experiments were conducted under the review of Institutional Review Board of the hospital.
TABLE-US-00001 TABLE 1 Patient No. 1 2 3 4 Gender Male Male Male Male Age 37 28 50 28 Diagnosis 18 24 32 20 Phenotype Classical Classical Classical Classical GLA activity 0.0% 0.6% 0.0% 0.6% GLA mutation c.803_806 c.658C > c.334C > c.1054T > c. del T T C GLA mutation p.L268fs* p.Arg220* p.Arg112Cys p.Trp349Arg p. 1 ERT duration 0 12 0 3 0 11 0 7 years years years years Serum GL3 18 4.8 16 8.3 10 5.5 12 5.6 (3.9-9.9 ug/ml) Angiokeratoma + + + + + + + + Cornea + + + + + + + + verticillata Sensorineural + + − + + + − − hearing loss EKG WPW WPW SB WPW SE SE WPW WPW abnormality Cardiac − − − − + + − − hypertrophy LV mass NA 89 89 98 126 153 94 105 (g/m.sup.2) Anhidrosis/ + + + + + + + + Hypohydrosis Acroparesthesia + + + + − − + + Proteinuria 11 106 0.03 73 109 98 72 35 (mg/day/m.sup.2) GFR 141 139 125 122 59 46 123 122 (ml/min/1.73 m.sup.2)
[0147] Fibroblasts were isolated from the obtained dermal tissue and cultured in DMEM supplemented with 10% fetal bovine serum (FBS), 1% penicillin-streptomycin and 1% non-essential amino acid. Then, FB-iPSC development was induced from the fibroblasts using a technique known in the art for ectopic expression by transduction of retrovirus expressing the pluripotent markers OCT4, SOX2, KLF4 and C-MYC (Takahashi, K et al, Cell 131(5): 861-872, 2007). The cells were cultured for 3 days, subcultured using mouse fetal fibroblasts as culture feeder cells, and cultured in DMEM/F12 medium supplemented with 20% KOSR (knockout serum replacement), 50 units/ml of penicillin-streptomycin, 0.1 mM non-essential amino acid, 1 mM L-glutamine, 0.1 mM β-mercaptoethanol and 10 ng/ml of basic fibroblast growth factor for a long time. Thereafter, a colony having the morphological characteristics similar to that of stem cells was isolated to construct an FB-iPSC cell line.
Experimental Example 1: Confirmation of Stem Cell Characteristics of iPSCs Derived from Patients with Fabry Disease
<1-1> Confirmation of Pluripotency of FB-IPSCs
[0148] In order to confirm whether the undifferentiated FB-iPSCs exhibit pluripotency, the expression of sternness markers in FB-iPSCs was confirmed using immunostaining.
[0149] Particularly, the FB-iPSCs prepared in Example 1 were fixed using a formaldehyde solution, and 0.1% triton X-100 was treated thereto to make the cell membrane permeable. Thereafter, the treated cells were washed three times with PBST (PBS containing Tween-20), to which and 4% normal donkey serum was added, followed by blocking at room temperature for 1 hour. Then, as the primary antibody, anti-OCT4 antibody (1:300, R&D Systems, USA), anti-SOX2 antibody (BD Transduction Laboratories, USA), anti-NANOG antibody (1:300, Cell signaling technology, USA), anti-SSEA-4 antibody (1:300, R&D Systems, USA), anti-TRA-1-81 antibody (1:300, Millipore, USA) or anti-TRA−1-60 antibody (1:300, Millipore, USA) was treated thereto and reacted at 4° C., followed by washing three times with PBST. After washing, Alexa Fluor 488 or Alexa Fluor 594-conjugated secondary antibody (Invitrogen, USA) was treated thereto and reacted at room temperature for 1 hour, followed by washing 6 times with PBST. At this time, the nuclei were fluorescently stained with DAPI (4′,6-diamidino-2-phenylindole) at the time of the last washing. Then, the expressions of OCT4, SOX2, NANOG, SSEA4, TRA-1-81 and TRA−1-60 proteins were confirmed by observing the stained FB-iPSCs under a fluorescence microscope (Olympus, Japan) or a Zeiss LSM 510 confocal microscope (Carl Zeiss, Germany).
[0150] As a result, as shown in
<1-2> Confirmation of Karyotype of FB-IPSCs
[0151] Karyotyping of the FB-iPSCs prepared in Example 1 was requested to GenDix (Korea), and it was confirmed that the FB-iPSCs prepared in Example 1 had a normal karyotype.
[0152] As shown in
Experimental Example 2: Confirmation of Decreased Activity of Alpha-Galactosidase (α-Galactosidase, GLA) in FB-iPSCs
[0153] In patients with Fabry disease, GLA activity should appear close to zero, so the GLA activity in FB-iPSCs was confirmed by the following method.
[0154] Particularly, 200 μl of GLA assay buffer (pH 4.6) containing 100 mM sodium citrate and 200 mM sodium phosphate dibasic was added to cell pellet of the FB-iPSCs prepared in Example 1, followed by sonication with a program of 1-second crushing and 1-second rest for a total of 10 seconds. Thereafter, a supernatant of the cell lysate was obtained by centrifugation at 1300 rpm for 30 minutes at 4° C. Then, a mixture for GLA analysis was prepared by mixing 30 μl of 200 mM N-acetyl-D-galactosamine (GalNAC), 6 μl of 50 mM 4-MU-α-D-galactopyranoside (4MUaGal), 14 μl of GLA assay buffer, and 10 of the obtained cell lysate supernatant. The prepared mixture was added to a 96 well plate, followed by incubation at 37° C. for 1 hour. Upon completion of the culture, the reaction was terminated by adding GLA stop buffer containing 200 mM glycine (pH 10.32) to each well, and fluorescence was confirmed at wavelengths of 355 and 460 nm using Victor plate reader (Perkin Elmer, USA).
[0155] As a result, as shown in
Experimental Example 3: Confirmation of Lysosome-Related Protein Expression Level in Patients with Fabry Disease
[0156] Since Fabry disease is classified as a lysosomal storage disease, the expression levels of lysosome-related proteins in each of FB-iPSCs and Fabry disease patient samples were confirmed by the following method.
<3-1> Confirmation of LC3 (Autophagy-Related Protein Light Chain 3) Protein Expression Level in FB-iPSCs
[0157] The expression level of the lysosome-related protein LC3 in FB-iPSCs was confirmed by Western blotting.
[0158] Particularly, the FB-iPSCs prepared in Example 1 were treated with Fabrazyme, a therapeutic agent for Fabry disease, and starvation media in various combinations. Pro-Prep solution (Intron Biotechnology, Korea) was added to each sample and reacted at 4° C., followed by centrifugation at 1300 rpm for 10 minutes to obtain a supernatant. The obtained supernatant was electrophoresed on acrylamide gel and transferred to a nitrocellulose membrane, followed by blocking with 4% skim milk. Then, anti-LC3 antibody (1:1000, Santacruz, USA) was treated thereto and reacted at 4° C. for 24 hours, followed by washing three times with TBS containing tween-20. The protein expression level was confirmed by the conventional Western blotting. The expression level of each protein was corrected using GAPDH as a control.
[0159] As a result, as shown in
<3-2> Confirmation of Expression Levels of LC3, Beclin 1 and Ubiquitin Proteins in Samples of Patients with Fabry Disease
[0160] The expression levels of LC3, Beclin 1 and ubiquitin proteins related to the lysosome signaling system in Fabry disease patient samples were confirmed by Western blotting.
[0161] Particularly, vascular endothelial cells were isolated from the dermal tissue obtained from the patients with Fabry disease of Example 1, to which Fabrazyme was treated. Then, the expression levels of LC3, Beclin 1 and ubiquitin proteins were confirmed by performing Western blotting in the same manner as described in Experimental Example <3-1>. At this time, anti-LC3 antibody (1:1000, Santacruz, USA), anti-Beclin 1 antibody (1:500, Santacruz, USA), and anti-ubiquitin antibody (1:1000, Santacruz, USA) were used as antibodies.
[0162] As a result, as shown in
[0163] From the above results, it was confirmed that the lysosomes did not function normally in patients with Fabry disease, and the characteristics of the lysosomal storage disease were not recovered even after the treatment of Fabrazyme, a therapeutic agent.
Example 2: Preparation of Vascular Endothelial Cells Derived from Patients with Fabry Disease
[0164] In order to confirm the vasculopathy of patients with Fabry disease, vascular endothelial cells were differentiated from FB-iPSCs according to the following method (
[0165] Particularly, the FB-iPSCs prepared in Example 1 were cultured in a feeder-free state for 3 days. Thereafter, the medium was exchanged with RPMI-1640 medium containing 1% B27, to which 50 ng/ml of activin A and 20 ng/ml of BPM4 were added as growth factors, and then the cells were cultured for 2 days to differentiate into mesoderm cells. The medium was exchanged with RPMI-1640 medium containing 0.5% B27, to which 50 ng/ml of VEGFA and 50 ng/ml of bFGF were added as growth factors, and then the cells were cultured for 2 days to differentiate into vascular progenitors. CD34 positive cells capable of differentiating into vascular endothelial cells were isolated from the induced vascular progenitors by performing magnetic activated cell sorting (MACS) using CD34 magnetic beads. The isolated CD34 positive cells were further cultured for 2 days in EGM-2 medium (Lonza, USA) containing 100 ng/ml of VEGF-A and 100 ng/ml of bFGF as growth factors to differentiate into vascular endothelial cells.
[0166] As a result, as shown in
Experimental Example 4: Confirmation of Characteristics of Vascular Endothelial Cells Derived from Patients with Fabry Disease
<4-1> Confirmation of Expression of Vascular Endothelial Cell Marker Protein
[0167] In order to confirm whether the vascular endothelial cells derived from Fabry disease patients were differentiated normally, the expression of the vascular endothelial cell marker proteins KDR (kinase insert domain receptor), CD31 and VE-cadherin (vascular endothelial cadherin) was confirmed using immunostaining. The experiment was carried out in the same manner as described in Experimental Example <1-1> using the vascular endothelial cells prepared in Example 2. At this time, anti-KDR antibody (1:300, Cell Signaling Technologies, USA), anti-CD31 antibody (1:300, Cell Signaling Technologies, USA), and anti-VE-cadherin antibody (1:300, Abcam, UK) were used as the primary antibodies.
[0168] Meanwhile, the distribution of cells expressing CD31 and CD105 among vascular endothelial cells was confirmed by FACS (fluorescence activated cell sorter). Particularly, the vascular endothelial cells prepared in Example 2 were treated with accutase and centrifuged to obtain a cell pellet. The cell pellet was resuspended in PBS containing 2% fetal bovine serum (FACS buffer), and the cells were filtered using a strainer having a pore size of 40 μm. The filtered cells were treated with anti-CD31 antibody (1:200, Biolegend, USA) and anti-CD105 antibody (1:200, Biolegend, USA) as FACS-specific antibodies, and reacted at 4° C. for 3 minutes. Upon completion of the reaction, the cells were washed 5 times with FACS buffer, and the cell distribution was confirmed using a FACS Caliber flow cytometer (BD biosciences).
[0169] As a result, as shown in
<4-2> Confirmation of Morphology and Vasculogenesis of Vascular Endothelial Cells
[0170] The changes in morphology of the vascular endothelial cells derived from patients with Fabry disease and the vasculogenesis were confirmed by the following method.
[0171] First, while culturing the vascular endothelial cells prepared in Example 2 for 13 days, the morphology of cells on the 9.sup.th, 11.sup.th, and 13.sup.th days was confirmed with a phase contrast microscope.
[0172] On the other hand, 70 μl of matrigel (corning) stock solution was put in a 96-well plate and hardened at 37° C., and then 1×10.sup.4 vascular endothelial cells prepared in Example 2 and EGM2 medium were added thereto to confirm the tube formation.
[0173] As a result, as shown in
Experimental Example 5: Confirmation of Decreased GLA Activity in Vascular Endothelial Cells Derived from Patients with Fabry Disease
[0174] The GLA activity in the vascular endothelial cells derived from patients with Fabry disease was confirmed by the following method. The experiment was carried out in the same manner as described in Experimental Example 2 using the vascular endothelial cells prepared in Example 2.
[0175] As a result, as shown in
Experimental Example 6: Confirmation of Expression of KDR Protein in Vascular Endothelial Cells Derived from Patients with Fabry Disease
[0176] Since Fabry disease causes vascular complications, the expression of KDR protein was confirmed by the following method to confirm the vasculopathy in patients with Fabry disease.
<6-1> Confirmation of Expression Site of KDR Protein
[0177] The expression site of KDR protein in the vascular endothelial cells differentiated from FE-iPSCs was confirmed by immunostaining. The experiment was carried out in the same manner as described in Experimental Example <1-1> using the vascular endothelial cells prepared in Example 2. At this time, anti-KDR antibody (1:300, Cell Signaling Technologies, USA) was used as the primary antibody.
[0178] As a result, as shown in
<6-2> Confirmation of KDR Protein Signaling System
[0179] The expression levels of KDR, eNOS (endothelial Nitric oxide synthase) and TSP1 (Thrombospondin type-1) related to the KDR protein signaling system in the vascular endothelial cells differentiated from FE-iPSCs were confirmed by Western blotting.
[0180] Particularly, the vascular endothelial cells prepared in Example 2 were treated with Fabrazyme, and Western blotting was performed in the same manner as described in Experimental Example <3-1>. At this time, anti-KDR antibody (1:1000, Cell Signaling Technologies, USA), anti-eNOS antibody (1:1000, Cell Signaling Technologies, USA) and anti-TSP1 antibody (1:1000, Santacruz, USA) were used as antibodies.
[0181] As a result, as shown in
Experimental Example 7: Confirmation of Expression of TSP1 Protein in Vascular Endothelial Cells Derived from Patients with Fabry Disease
[0182] To determine whether the vascular-related complications of Fabry disease are caused by overexpression of TSP1 protein, the signaling system of TSP1 protein was confirmed by the following method.
<7-1> Confirmation of TGF-β (Transforming Growth Factor Beta) Activation
[0183] In order to confirm the activation of TGF-β protein, an upper signaling system of TSP1 protein in the vascular endothelial cells differentiated from FB-iPSCs, the phosphorylation of SMAD2 protein was confirmed using Western blotting.
[0184] Particularly, the vascular endothelial cells prepared in Example 2 were treated with Fabrazyme, and Western blotting was performed in the same manner as described in Experimental Example <3-1>. At this time, anti-SMAD2 antibody (1:1000, Cell Signaling Technologies, USA) and anti-phospho-SMAD2 antibody (1:1000, Cell Signaling Technologies, USA) were used as antibodies.
[0185] As a result, as shown in
<7-2> Confirmation of Increase in Expression Level of TSP1 Protein by Activation of TGF-β
[0186] In order to confirm whether the activation of TGF-β increases the expression level of TSP1 protein, the expression levels of the related proteins including TSP-1 protein were confirmed using Western blotting.
[0187] Particularly, the vascular endothelial cells differentiated from normal iPSCs were treated with activin A to activate TGF-β, and Western blotting was performed in the same manner as described in Experimental Example <3-1>. At this time, anti-TSP1 antibody (1:1000, Santacruz, USA), anti-phospho-SMAD2 antibody (1:1000, Cell Signaling Technologies, USA), anti-SMAD2 antibody (1:1000, Cell Signaling Technologies, USA), anti-KDR antibody (1:1000, Cell Signaling Technologies, USA), anti-eNOS antibody (1:1000, Cell Signaling Technologies, USA), anti-bFGF antibody (1:1000, Bioss, USA), anti-ANG2 antibody (1:1000, Bioss, USA) and anti-vEGF antibody (1:1000, Santacruz, USA) were used as antibodies.
[0188] As a result, as shown in
<7-3> Confirmation of Expression Location of TSP1 Protein
[0189] The expression location of TSP1 protein in the vascular endothelial cells differentiated from FB-iPSCs was confirmed by immunostaining. The experiment was performed in the same manner as described in Experimental Example <1-1> using the vascular endothelial cells prepared in Example 2. Anti-TSP1 antibody (1:200, Santacruz, USA) was used as the primary antibody.
[0190] As a result, as shown in
Experimental Example 8: Confirmation of Vasculopathy Induced by Gb3 (Globotriaosylceramide 3) Protein
[0191] Whether the Gb3 protein accumulated in cells and organs of patients with Fabry disease induces vasculopathy was confirmed by the following method.
<8-1> Confirmation of Changes in Morphology of Vascular Endothelial Cells
[0192] The changes in the morphology of vascular endothelial cells caused by Gb3 protein was confirmed by the following method.
[0193] Particularly, the vascular endothelial cells differentiated from normal iPSCs were treated with LysoGb3 protein (MATREYA LLC, USA) for 9 days, and then the morphology of the cells was confirmed.
[0194] As a result, as shown in
<8-2> Confirmation of Expression Levels of Vasculopathy-Related Genes
[0195] The changes in the expression levels of vasculopathy-related genes by Gb3 protein were confirmed using RT-PCR (reverse transcription polymerase chain reaction).
[0196] Particularly, the vascular endothelial cells differentiated from normal iPSCs were treated with LysoGb3 protein for 1, 3 or 5 days, and RNA was extracted from the cells using easy-BLUE (Intron). Then, RT-PCR was performed in the conventional manner to confirm the RNA expression levels of KDR, eNOS and TSP1 (Thrombospondin 1) genes related to vasculopathy. As a result, as shown in
<8-3> Confirmation of Expression Levels of Vasculopathy-Related Proteins
[0197] The changes in the expression levels of vasculopathy-related proteins by Gb3 protein were confirmed using Western blotting. Particularly, the vascular endothelial cells differentiated from normal iPSCs were treated with LysoGb3 protein for 3, 6, or 9 days, and Western blotting was performed in the same manner as described in Experimental Example <3-1>. At this time, anti-TSP1 antibody (1:1000, Santacruz, USA), anti-KDR antibody (1:1000, Cell Signaling Technologies, USA), anti-eNOS antibody (1:1000, Cell Signaling Technologies, USA), anti-AKT antibody (1:1000, Cell Signaling Technologies, USA), and anti-phospho-AKT antibody (1:1000, Cell Signaling Technologies, USA) were used as antibodies.
[0198] As a result, as shown in
<8-4> Confirmation of Expression Location of TSP1 Protein
[0199] The expression location of TSP1 protein in the vascular endothelial cells differentiated from FE-iPSCs was confirmed by immunostaining. After treating the vascular endothelial cells differentiated from normal iPSCs with LysoGb3 protein, the experiment was performed in the same manner as described in Experimental Example <1-1>. Anti-TSP1 antibody (1:200, Santacruz, USA) was used as the primary antibody.
[0200] As a result, as shown in
[0201] From the above results, it was confirmed that the Gb3 protein is a major substance causing vasculopathy in patients with Fabry disease.
Experimental Example 9: Confirmation of Therapeutic Effect of TGF-β Inhibitor on Vasculopathy of Patients with Fabry Disease
<9-1> Confirmation of Changes in Morphology of Vascular Endothelial Cells by SB431542
[0202] The changes in morphology of vascular endothelial cells by SB431542, a TGF-β inhibitor, were confirmed by the following method.
[0203] Particularly, using the control group treated with only Fabrazyme on the vascular endothelial cells prepared in Example 2, the experimental group treated with only SB431542 (Cayman Chemical, USA), and the experimental group treated with Fabrazyme and SB431542, the morphology of the cells was confirmed.
[0204] As a result, as shown in
<9-2> Confirmation of Signaling System of Vascular Endothelial Cells by SB431542
[0205] The changes in the expression levels of vasculopathy-related proteins by SB431542 were confirmed using Western blotting.
[0206] Particularly, using the control group treated with only Fabrazyme on the vascular endothelial cells prepared in Example 2 and the experimental group treated with Fabrazyme and SB431542, Western blotting was performed in the same manner as described in Experimental Example <3-1>. At this time, anti-TSP1 antibody (1:1000, Santacruz, USA), anti-KDR antibody (1:1000, Cell Signaling Technologies, USA) and anti-eNOS antibody (1:1000, Cell Signaling Technologies, USA) were used as antibodies.
[0207] As a result, as shown in
<9-3> Confirmation or Vasculogenesis of Vascular Endothelial Cells by SB431542
[0208] Vasculogenesis of vascular endothelial cells caused by SB431542 was confirmed by the following method.
[0209] Particularly, using the control group treated with only Fabrazyme on the vascular endothelial cells prepared in Example 2, the experimental group treated with only SB431542, and the experimental group treated with Fabrazyme and SB431542, The tube formation was confirmed in the same manner as described in Experimental Example <4-2>.
[0210] As a result, as shown in
<9-4> Confirmation of Changes in Morphology of Vascular Endothelial Cells by Losartan
[0211] The changes in morphology of vascular endothelial cells by losartan, a TGF-β inhibitor, were confirmed by the following method.
[0212] Particularly, using the control group treated with only Fabrazyme on the vascular endothelial cells prepared in Example 2, the experimental group treated with Fabrazyme and SB431542, and the experimental group treated with Fabrazyme and losartan (Cayman Chemical, USA), the morphology of the cells was confirmed.
[0213] As a result, as shown in
[0214] From the above results, SB431542 showed a therapeutic effect on vasculopathy in patients with Fabry disease, but the effect of losartan could not be confirmed.
Example 3: Preparation of FB-iPSC Isotype Control Cell Line
[0215] For objective experiments on vasculopathy of patients with Fabry disease, a FB-iPSC isotype control cell line was prepared using CRISPR/CAS9 system (
[0216] Particularly, in the FB-iPSCs prepared in Example 1, a defect in GLA gene was corrected by the conventional method using CRISPR/CAS9 system targeting the sequences shown in Table 2 below. An edited cell line was prepared using the target 2, which has a higher indel frequency for the target (Table 3), and DNA was extracted therefrom, followed by sequencing thereof.
TABLE-US-00002 TABLE 2 SEQ. CRISPR/CAS9 ID. target gene Nucleotide sequence (5′-3′) NO: GLA (target 1) TCATTCTTTTTCTCAGTNNNNGATTGG 3 GLA (target 2) TTCTCAGTNNNNGATTGGCAACTTTGG 4
TABLE-US-00003 TABLE 3 Total Indel HDR reads Insert Deletion (%) (%) Target Cas9 alone 23233 0 3 3 0 1 (0.0%) (0.0%) Cas9 + T1_sgRNA 22041 0 0 0 0 (0.0%) (0.0%) Cas9 + T1_ 24833 0 0 0 0 sgRNA + ssODN (0.0%) (0.0%) Target Cas9 alone 23226 0 13 13 0 2 (0.1%) (0.0%) Cas9 + T2_sgRNA 22636 339 2716 3055 0 (13.5%) (0.0%) Cas9 + T2_ 21316 1318 1766 3084 877 sgRNA + ssODN (14.5%) (4.1%)
[0217] As a result, as shown in
Example 4: Preparation of Vascular Endothelial Cells Differentiated from Isotype Control Cells of FB-iPSCs
[0218] Vascular endothelial cells were prepared by differentiating the FB-iPSC isotype control cells prepared in Example 3 in the same manner as described in Example 2.
Experimental Example 10: Confirmation of Recovery of GLA Activity in FB-iPSC Isotype Control Cell Line and Vascular Endothelial Cells
[0219] Whether the GLA activity was recovered in the FB-iPSC isotype control cell line and the vascular endothelial cells differentiated therefrom was confirmed by the following method. The experiment was performed in the same manner as described in Experimental Example 2 using the FB-iPSC isotype control cell line prepared in Example 3 and the vascular endothelial cells prepared in Example 4.
[0220] As a result, as shown in
Experimental Example 11: Confirmation of Recovery of Vasculopathy in Vascular Endothelial Cells Differentiated from FB-iPSC Isotype Control Cells
<11-1> Confirmation of Expression Levels of Vasculopathy-Related Proteins
[0221] The expression levels of vasculopathy-related proteins in the vascular endothelial cells differentiated from FB-iPSC isotype control cells were confirmed by Western blotting. Western blotting was performed in the same manner as described in Experimental Example <3-1> using the vascular endothelial cells prepared in Example 2 and the vascular endothelial cells prepared in Example 4 treated with GLA (Genzyme, USA). At this time, anti-TSP1 antibody (1:1000, Santacruz, USA), anti-SMAD2 antibody (1:1000, Cell Signaling Technologies, USA), anti-phospho-SMAD2 antibody (1:1000, Cell Signaling Technologies, USA), anti-KDR antibody (1:1000, Cell Signaling Technologies, USA) and anti-eNOS antibody (1:1000, Cell Signaling Technologies, USA) were used as antibodies.
[0222] As a result, as shown in
<11-2> Confirmation of Expression Location of Anti-Vasculogenesis Factor Protein
[0223] The expression location of the anti-vasculogenesis factor protein in the vascular endothelial cells differentiated from FB-iPSC isotype control cells was confirmed by immunostaining.
[0224] Particularly, the experiment was performed in the same manner as described in Experimental Example <1-1> using the vascular endothelial cells prepared in Example 2 and the vascular endothelial cells prepared in Example 4 treated with GLA. Anti-VE-cadherin antibody (1:300, Abcam, UK) and anti-TSP1 antibody (1:200, Santacruz, USA) were used as the primary antibodies.
[0225] As a result, as shown in
<11-3> Confirmation of Vasculogenesis of Vascular Endothelial Cells
[0226] Vasculogenesis of the vascular endothelial cells differentiated from FB-iPSC isotype control cells was confirmed by the following method. The experiment was performed in the same manner as described in Experimental Example <4-2> using the vascular endothelial cells prepared in Example 2 and the vascular endothelial cells prepared in Example 4 treated with GLA.
[0227] As a result, as shown in
[0228] From the above results, it was confirmed that the correction of GLA gene restored vasculopathy in patients with Fabry disease.
Example 5: Construction of TSP1 Gene Knocked-Out FB-iPSC Cell Line
[0229] An FB-iPSC cell line in which TSP1 gene known as the cause of vasculopathy in Fabry disease patients was knocked out was constructed using CRISPR/CAS9 system (
[0230] Particularly, the TSP1 gene of the FB-iPSCs prepared in Example 1 was knocked out by the conventional method using CRISPR/CAS9 system targeting the sequences shown in Table 4 below. A knockout cell line was prepared using the target 2, which has a higher indel frequency for the target (Table 5), and DNA was extracted therefrom, followed by sequencing thereof.
TABLE-US-00004 TABLE 4 SEQ. CRISPR/CAS9 ID. target gene Nucleotide sequence (5′-3′) NO: TSP1 (target 1) GTCTGTGGAAGAAGCTCTCCTGG 5 TSP2 (target 2) CTGGAGCGGAAAGACCACTCTGG 6
TABLE-US-00005 TABLE 5 Total reads Insert Deletion Indel (%) Target 1 Cas9 alone 28429 0 9 9 (0.0%) Cas9 + T1_sgRNA 17769 117 1154 1271 (7.2%) Target 2 Cas9 alone 27483 0 3 3 (0.0%) Cas9 + T2_sgRNA 21243 198 1880 2078 (9.8%)
[0231] As a result, as shown in
Example 6: Preparation of Vascular Endothelial Cells Differentiated from TSP1 Gene Knocked-Out FB-iPSC Cells
[0232] Vascular endothelial cells were prepared by differentiating the TSP1 gene knocked-out FB-iPSC cells prepared in Example 5 in the same manner as described in Example 2.
Experimental Example 12: Confirmation of Recovery of Vasculopathy in Vascular Endothelial Cells Differentiated from TSP1 Gene Knocked-Out FB-iPSC Cells
<12-1> Confirmation of Changes in Morphology of Vascular Endothelial Cells
[0233] The changes in the morphology of the vascular endothelial cells differentiated from TSP1 gene knocked-out FB-iPSC cells were confirmed by the following method. In the experiment, the vascular endothelial cells prepared in Example 2 and the vascular endothelial cells prepared in Example 6 treated with GLA were used to confirm the cell morphology.
[0234] As a result, as shown in
<12-2> Confirmation of Expression Level of TSP1 Gene in Vascular Endothelial Cells
[0235] The RNA expression level of TSP1 gene in the vascular endothelial cells differentiated from TSP1 gene knocked-out FB-iPSC cells was confirmed by RT-PCR. Particularly, RT-PCR was performed in the same manner as described in Experimental Example <8-2> using the vascular endothelial cells prepared in Example 2 and the vascular endothelial cells prepared in Example 6.
[0236] As a result, as shown in
<12-3> Confirmation of Expression Levels of Vasculopathy-Related Proteins
[0237] The expression levels of vasculopathy-related proteins in the vascular endothelial cells differentiated from TSP1 gene knocked-out FB-iPSC cells were confirmed by Western blotting. Particularly, Western blotting was performed in the same manner as described in Experimental Example <3-1> using the vascular endothelial cells prepared in Example 2 and the vascular endothelial cells prepared in Example 6. Anti-TSP1 antibody (1:1000, Santacruz, USA), anti-KDR antibody (1:1000, Cell Signaling Technologies, USA), anti-eNOS antibody (1:1000, Cell Signaling Technologies, USA), anti-phospho-SMAD2 antibody (1:1000, Cell Signaling Technologies, USA) and anti-SMAD2 antibody (1:1000, Cell Signaling Technologies, USA) were used as antibodies.
[0238] As a result, as shown in
<12-4> Confirmation of Vasculogenesis of Vascular Endothelial Cells
[0239] Vasculogenesis of the vascular endothelial cells differentiated from TSP1 gene knocked-out FB-iPSC cells was confirmed by the following method. The experiment was performed in the same manner as described in Experimental Example <4-2> using the vascular endothelial cells prepared in Example 2 and the vascular endothelial cells prepared in Example 4 treated with GLA.
[0240] As a result, as shown in
[0241] From the above results, it was confirmed that the TSP1 protein is a major protein causing vasculopathy in patients with Fabry disease, and the inhibition of its expression could cure Fabry disease.