PHARMACEUTICAL COMPOSITION COMPRISING PEPTIDE THAT INHIBITS INTERACTION OF P53 AND FOXO4

Abstract

Provided is a method for preventing, ameliorating, or treating degenerative diseases caused by cellular senescence, preferably osteoarthritis or atherosclerosis, comprising a specific peptide as an active ingredient, where the peptide remarkably inhibits the interaction of p53 and FOXO4 (Forkhead box protein O4), thereby inhibiting the expression of a cellular senescence regulator.

Claims

1. A method for preventing, improving or treating a degenerative disease caused by cellular senescence, comprising a peptide consisting of three amino acids of the following Formula 1 as an active ingredient:
Leu-X-Asp   <Formula 1> wherein, X is glutamic acid (Glu), serine (Ser), glycine (Gly), alanine (Ala), glutamine (Gln), arginine (Arg), lysine (Lys), leucine (Leu), tyrosine (Tyr), aspartic acid (Asp), phenylalanine (Phe), asparagine (Asn), cysteine (Cys), histidine (His), isoleucine (Ile), methionine (Met), proline (Pro), threonine (Thr), tryptophan (Trp) , or valine (Val), and is a peptide bond.

2. The method according to claim 1, wherein the peptide is a peptide consisting of the amino acid sequence of SEQ ID NO: 1, 3, 4, 5, 7, 8, 9, 11, 13, 14, 15, 17, 18, 19 or 20.

3. The method according to claim 1, wherein the degenerative disease caused by cellular senescence is osteoarthritis or atherosclerosis.

4. The method according to claim 2, wherein the degenerative disease caused by cellular senescence is osteoarthritis or atherosclerosis.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0014] FIG. 1 shows the results obtained by evaluating the effects on the interaction between p53 and FOXO4 when human keratinocytes (HaCaTs) were treated with the peptides of the present invention and active oxygen species (H.sub.2O.sub.2).

[0015] FIG. 2 shows the results obtained by evaluating the effects of ERK and SHP2 activation by the peptide on the interaction of p53 and FOXO4, through treating human keratinocytes (HaCaTs) with the peptide of the present invention, active oxygen species (H.sub.2O.sub.2), the ERK inhibitor, and the SHP2 inhibitor.

[0016] FIG. 3 shows the results obtained by evaluating, through β-Galactosidase staining, the effects on apoptosis of the senescent cells induced by active oxygen species, when human retinal pigment epithelial cells (ARPE-19) were treated with the peptide of the present invention and active oxygen species (H.sub.2O.sub.2).

[0017] FIG. 4 shows the results of quantitative analysis on the numbers of the remaining senescent cells confirmed through the β-Galactosidase staining in FIG. 3.

BEST MODE

[0018] As used herein, the term “degenerative diseases” refers to diseases caused by cellular senescence, including e.g., atherosclerosis, osteoarthritis, Alzheimer's disease, Parkinson's disease, chronic obstructive pulmonary disease, idiopathic pulmonary fibrosis, retinopathy, etc., and preferably osteoarthritis and atherosclerosis.

[0019] The present invention provides a pharmaceutical composition for preventing, improving or treating a degenerative disease caused by cellular senescence, comprising a peptide consisting of three amino acids of the following Formula 1 as an active ingredient:

Leu-X-Asp   <Formula 1>

[0020] wherein,

[0021] X is glutamic acid (Glu), serine (Ser), glycine (Gly), alanine (Ala), glutamine (Gln), arginine (Arg), lysine (Lys), leucine (Leu), tyrosine (Tyr), aspartic acid (Asp), phenylalanine (Phe), asparagine (Asn), cysteine (Cys), histidine (His), isoleucine (Ile), methionine (Met), proline (Pro), threonine (Thr), tryptophan (Trp) , or valine (Val), and [0022] is a peptide bond.

[0023] In the pharmaceutical composition according to the present invention, the peptide consisting of the amino acid sequence of SEQ ID NO: 1, 3, 4, 5, 7, 8, 9, 11, 13, 14, 15, 17, 18, 19, or 20 has been found to have a particularly excellent activity in inhibiting the interaction between p53 and FOXO4. Accordingly, in an embodiment, the peptide may be a peptide consisting of the amino acid sequence of SEQ ID NO: 1, 3, 4, 5, 7, 8, 9, 11, 13, 14, 15, 17, 18, 19, or 20.

[0024] The pharmaceutical composition of the present invention may include a pharmaceutically acceptable carrier, for example additives such as lactose or corn starch, lubricants such as magnesium stearate, currently available emulsifiers, suspending agents, buffers, isotonic agents, etc. The pharmaceutical composition of the present invention can be formulated to an oral dosage form or a parenteral dosage form, preferably to a parenteral dosage form for transdermal administration, subcutaneous administration, intramuscular administration, etc. For example, for intramuscular, subcutaneous and intravenous dosage forms, sterile solutions of the active ingredient are usually prepared and may contain a buffer capable of adjusting the pH of the solution appropriately. For intravenous administration, an isotonic agent may be included so as to render the formulation isotonic. And, the composition of the present invention may be in the form of an aqueous solution containing pharmaceutically acceptable carriers, e.g., saline having a pH level of 7.4. The solutions may be introduced into a patient's intramuscular blood-stream by local bolus injection. The pharmaceutical composition of the present invention may be administered to a patient in an amount suitable for preventing, improving, or treating a degenerative disease, e.g., at a daily dosage of about 0.01 to 10 mg/kg, which may be generally changed according to the age, body weight, and conditions of a patient.

[0025] Hereinafter, the present invention will be described more specifically by the following examples and experimental examples. However, the following examples and experimental examples are provided only for illustrations and thus the present invention is not limited to or by them.

EXAMPLE 1

Synthesis of Peptides

[0026] The peptides of SEQ ID NOs: 1 to 20 (see Table 1 below) were synthesized with an automatic peptide synthesizer (PeptrEx-R48, Peptron, Daejeon, Korea) using a FMOC solid-phase method. The synthesized peptide fragments were purified and analyzed by reverse-phase high-performance liquid chromatography (reverse-phase HPLC) (Prominence LC-20AB, Shimadzu, Japan) using a C18 analytical RP column (Shiseido capcell pak), and identified using a mass spectrometer (HP 1100 Series LC/MSD, Hewlett-Packard, Roseville, U.S.A.).

TABLE-US-00001 TABLE 1 Peptide name SEQ ID NO Amino acid sequence Pep1 SEQ ID NO: 1 Leu-Glu-Asp Pep2 SEQ ID NO: 2 Leu-Ser-Asp Pep3 SEQ ID NO: 3 Leu-Gly-Asp Pep4 SEQ ID NO: 4 Leu-Ala-Asp Pep5 SEQ ID NO: 5 Leu-Gln-Asp Pep6 SEQ ID NO: 6 Leu-Arg-Asp Pep7 SEQ ID NO: 7 Leu-Lys-Asp Pep8 SEQ ID NO: 8 Leu-Leu-Asp Pep9 SEQ ID NO: 9 Leu-Tyr-Asp Pep10 SEQ ID NO: 10 Leu-Asp-Asp Pep11 SEQ ID NO: 11 Leu-Phe-Asp Pep12 SEQ ID NO: 12 Leu-Asn-Asp Pep13 SEQ ID NO: 13 Leu-Cys-Asp Pep14 SEQ ID NO: 14 Leu-His-Asp Pep15 SEQ ID NO: 15 Leu-Ile-Asp Pep16 SEQ ID NO: 16 Leu-Met-Asp Pep17 SEQ ID NO: 17 Leu-Pro-Asp Pep18 SEQ ID NO: 18 Leu-Thr-Asp Pep19 SEQ ID NO: 19 Leu-Trp-Asp Pep20 SEQ ID NO: 20 Leu-Val-Asp

EXAMPLE 2

Preparation of the Compositions Containing Peptides

[0027] The peptides of SEQ ID NOs: 1 to 20 were respectively dissolved in phosphate buffered saline (PBS) to a concentration of 1 M. The resultant protein solutions were also used in the following experimental examples.

EXPERIMENTAL EXAMPLE 1

Evaluation of the Effects of Peptides on the Physical Binding Between p53 and FOXO4

[0028] After treating cells with the peptides of the present invention, the effects thereof on the physical binding between p53 and FOXO4 were evaluated through an in situ PLA (proximity ligation assay) method. HaCaT cells (human keratinocytes, CLS) were added at 4.5×10.sup.4 cells per well, along with a DMEM containing 10% fetal bovine serum, to each well of a 24-well microplate and then cultured at 37° C. in a 5% CO.sub.2 incubator for 24 hours. H.sub.2O.sub.2 and the peptide solutions of Example 2 and H.sub.2O.sub.2 were added thereto so that the concentrations of H.sub.2O.sub.2 and each peptide in the medium were 200 μM and 20 μM respectively, followed by incubating for 1 hour under the same condition. As a control group, an untreated group (indicated by “control” in FIG. 1) and a group treated with H.sub.2O.sub.2 alone (indicated by “-” in FIG. 1) were used. The cells of each well were washed with PBS, fixed by treating with 2% formaldehyde for 15 minutes, and then treated with 0.1% TritonX-100 for 5 minutes to increase antibody permeability into the cells. Anti-p53 polyclonal antibody (Abcam, UK) and anti-FOXO4 polyclonal antibody (Santa Cruz, Calif., USA) were added thereto. After the PLA probe was added thereto using the in situ PLA kit (Sigma-Aldrich), hybridization, ligation, amplification and mounting steps were carried out according to the manufacturer's protocol. Each physical interaction between p53 and FOXO4 was quantified by measuring the luminescence signals (PLA signals) detected in each cell with a confocal laser microscope (Olympus fluoview FW1000; Olympus, Tokyo, Japan). The results thereof are shown in FIG. 1. From the results of FIG. 1, it can be confirmed that the groups treated with the peptides of the present invention significantly inhibited the interaction between p53 and FOXO4, in comparison with the untreated control group. In particular, it can be confirmed that Pep 1, 3, 4, 5, 7, 8, 9, 11, 13, 14, 15, 17, 18, 19, or 20 (i.e., the peptides of SEQ ID NOs: 1, 3, 4, 5, 7, 8, 9, 11, 13, 14, 15, 17, 18, 19, or 20) remarkably inhibited the interaction between p53 and FOXO4, in comparison with the control group, and that Pep 1, 9, 11, 14, 15, 17, 18, and 20 (i.e., peptides of SEQ ID NOs: 1, 9, 11, 14, 15, 17, 18, and 20) remarkably inhibited the interaction between p53 and FOXO4 by two or more times, in comparison with the control group.

EXPERIMENTAL EXAMPLE 2

Evaluation of the Effects of ERK and SHP2 on the Inhibitory Signal of Physical Binding Between p53 and FOXO4 by the Peptide

[0029] After treating cells with the peptide of the present invention (the peptide of SEQ ID NO: 3), H.sub.2O.sub.2, a ERK inhibitor (PD98059), and a SHP2 inhibitor (NSC878777), the effects thereof on the physical binding between p53 and FOXO4 were evaluated through an in situ PLA (proximity ligation assay) method. HaCaT cells (human keratinocytes, CLS) were added at 4.5×10.sup.4 cells per well, along with a DMEM containing 10% fetal bovine serum, to each well of a 24-well microplate and then cultured at 37° C. in a 5% CO.sub.2 incubator for 24 hours. The cells were treated with H.sub.2O.sub.2 (200 μM) and the peptide of SEQ ID NO: 3 (20 μM); or PD98059 (10 μM) or NSC878777 (10 μM) was additionally treated to the cells treated with H.sub.2O.sub.2 (200 μM) and the peptide of SEQ ID NO: 3 (20 μM), followed by incubating for 1 hour under the same condition. As a control group, an untreated group (indicated by “control” in FIG. 2) and a group treated with H.sub.2O.sub.2 alone were used. The cells of each well were washed with PBS, fixed by treating with 2% formaldehyde for 15 minutes, and then treated with 0.1% TritonX-100 for 5 minutes to increase antibody permeability into the cells. Anti-p53 polyclonal antibody (Abcam, UK) and anti-FOXO4 polyclonal antibody (Santa Cruz, Calif., USA) were added thereto. After the PLA probe was added thereto using the in situ PLA kit (Sigma-Aldrich), hybridization, ligation, amplification and mounting steps were carried out according to the manufacturer's protocol. Each physical interaction between p53 and FOXO4 was quantified by measuring the luminescence signals (PLA signals) detected in each cell with a confocal laser microscope (Olympus fluoview FW1000; Olympus, Tokyo, Japan). The results thereof are shown in FIG. 2. From the results of FIG. 2, it can be confirmed that the groups treated with the peptide of the present invention significantly inhibited the interaction between p53 and FOXO4 in comparison with the untreated control group; and that the inhibitory signal by the peptide is dependent on ERK and SHP2 activation.

EXPERIMENTAL EXAMPLE 3

Evaluation of the Activities of Peptide on the Apoptosis Induction of Senescent Cells Through Increase in p53 Activity

[0030] In order to evaluate the activity on the apoptosis of senescent cells by the treatment with the peptide of the present invention (the peptide of SEQ ID NO: 3) for 24 hours after inducing senescence by treating cells with H.sub.2O.sub.2, the X-Gal staining was carried out to measure the number of the remaining senescent cells. ARPE-19 cells (retinal pigment epithelial cells) were added at the density of 80% per well, along with a DMEM containing 10% fetal bovine serum, to each well of a 12-well microplate and then cultured at 37° C. in a 5% CO.sub.2 incubator for 24 hours. H.sub.2O.sub.2 was added thereto so that the concentration thereof in the medium was 25 μM, followed by incubating for 24 hours under the same condition. Thereafter, the cells in each well were washed with PBS and the peptide solution of Example 2 was added thereto so that the concentration of the peptide of SEQ ID NO: 3 was 0.2 μM, 2 μM, and 20 μM respectively, followed by incubating for 24 hours under the same condition. As a control group, an untreated group (indicated as “control” in FIGS. 3 and 4) and a group treated with H.sub.2O.sub.2 alone (indicated by “-” in FIGS. 3 and 4) were used. The cells in each well were washed with PBS, and X-gal staining was performed using the Senescence β-Galactosidase Staining Kit (CST) according to the manufacturer's protocol. The bluish green color development detected in the senescence-induced cells was measured with a phase-contrast microscope (Olympus, Tokyo, Japan), and each number of senescent cells was quantified. The results are shown in FIGS. 3 and 4. From the results of FIGS. 3 and 4, it can be confirmed that the groups treated with the peptide of the present invention significantly induced the apoptosis of senescent cells, in comparison with the untreated control group (i.e., the “-” group).