Method for increasing stemness of human mesenchymal stem cells

Abstract

The present invention relates to a method for increasing the stemness of human mesenchymal stem cells and, more particularly, to: a method for increasing the stemness of human mesenchymal stem cells by means of endothelin-1 treatment; the human mesenchymal stem cells having increased stemness by using the method; and a composition for increasing the stemness of human mesenchymal stem cells, containing endothelin-1 as an active ingredient. In the present invention, it is confirmed that the expression of a stemness marker is increased and that a stem cell characteristic is improved such as the length of telomeres being extended, by treating human mesenchymal stem cells with endothelin-1, and thus cellular life span is extended, aging is inhibited, and the growth and viability of cells are increased, thereby enabling mass culturing of human mesenchymal stem cells such that human mesenchymal stem cells are expected to be used effectively in cell therapy or regenerative medicine.

Claims

1. A method for extending telomere length in human mesenchymal stem cells, comprising: treating a culture broth of human mesenchymal stem cells with endothelin-1 at a concentration of 0.026 to 0.125 g/mL to culture the human mesenchymal stem cells.

2. The method of claim 1, wherein the stem cells treated with endothelin-1 comprise an increased lifespan of human mesenchymal stem cells.

3. The method of claim 1, wherein the method comprises treating the culture broth of the stem cells with the endothelin-1 after 24 hours of an adhesion culture of the mesenchymal stem cells.

Description

DESCRIPTION OF DRAWINGS

(1) FIG. 1 shows results of determining, through western blotting, a level of expression of an Oct4 protein in human mesenchymal stem cells (MSCs) when the MSCs are treated with endothelin-1 (ET-1).

(2) FIG. 2 shows results of determining, through real time PCR, a level of expression of Oct4 mRNA in human MSCs when the MSCs are treated with ET-1.

(3) FIG. 3 shows results of real time gDNA PCR using gDNA obtained from human MSCs treated with ET-1.

(4) FIG. 4 shows results of determining chromosomal stability of human MSCs treated with ET-1 using a G-banding karyotype analysis method.

BEST MODE

(5) The present invention is characterized by providing a method for increasing stemness of human mesenchymal stem cells (MSCs). For this purpose, the method includes treating a culture broth of stem cells with endothelin-1 (ET-1) to culture the stem cells.

(6) The present inventors have conducted research to solve the prior-art problem of stem cells whose stemness decreases with an increase in the number of passages thereof when human MSCs are passaged, and identified that the stemness of the stem cells is improved when a culture broth of human MSCs is treated with ET-1.

(7) Oct4, Nanog, Sox2, c-Myc, KLF4, and the like have been known as stemness-related markers. Such stemness-related markers have been effectively used for research because it can be seen that stem cells have a higher culture yield and characteristics of the stem cells are more excellently maintained as the stemness-related markers are expressed at a higher level of expression. In particular, Oct4 known to be expressed by undifferentiated stem cells serves to prevent cell differentiation, and is known to disappear when natural differentiation of cells is started. Therefore, a degree of differentiation of the stem cells may be expected depending on a level of expression of Oct4.

(8) According to one exemplary embodiment of the present invention, a culture broth of human MSCs is treated with various concentrations of ET-1, and a expression level of Oct-4 is measured. As a result, it is confirmed that levels of protein and mRNA expression of Oct-4 whose level of expression has decreased increase with an increase in the number of passages (see FIGS. 1 and 2). These results suggest that the stemness of human MSCs is restored when the human MSCs are treated with ET-1. Also, it can be seen that the method of the present invention may be effectively applied to cell therapy and regenerative medicine because it is identified that ET-1 may increase expression of stemness markers such as Oct4 and the like.

(9) Also, a length of telomeres may be determined using another method of determining an improvement of stemness. Telomeres are found at the termini of eukaryotic chromosomes and have a unique structure to prevent chromosomal breakage or end-to-end fusion. Telomeric DNA has a primary structure consisting of tandem repeats of short base sequences (TTAGGG in the case of humans) and has a varying length spanning from several hundreds of base pairs in the case of lower eukaryotic cells to several thousands of base pairs in the case of mammalian cells. A telomeric DNA region has a GC imbalance (GC-rich) as in a centromeric region. When a chromosome is replicated, such a nature of telomeric DNA causes incomplete replication of a G-strand thereof by conventional DNA polymerases so that an exposed complementary strand (C-strand) is degraded by a nucleotide removal enzyme or a telomeric end region thereof may be finished through synthesis using a telomerase. Main functions of telomeres are to cap ends of chromosomes and protect the chromosomes from breakage, end-to-end fusion, and heterologous recombination, which are associated with maintenance of safety of genomes and regulation of growth of cells. Telomere shortening occurs with repeated cell divisions, which activates cell cycle restriction points, which induce replicative senescence and apoptosis, to restrict the growth of cells. The telomere shortening has an advantageous effect of preventing accumulation of genetically unstable cells or altered cells from which cancer arises, but also has an adverse effect of restricting homeostasis of, regeneration of, and survival of organs when the aging and diseases occur. A decline in tissue regeneration function due to telomere shortening is associated with stem cell dysfunction, and telomere dysfunction induces impaired functions of stem cells by not only activating the stem cells' own restriction points but also changing all micro- and macro-environments surrounding the stem cells (E Hiyama et al., British Journal of Cancer, 96: 1020-1024, 2007).

(10) Therefore, according to one exemplary embodiment of the present invention, after adhesion-cultured MSCs are treated with ET-1 and cultured for 24 hours or more, a length of telomeres thereof is compared to that of a group (control) in which MSCs are not treated with ET-1. As a result, it is confirmed that, when the human MSCs are treated with ET-1, the length of the telomeres, that is, end regions of chromosomes, may be extended (see FIG. 3), and the ET-1 treatment causes no chromosomal abnormality (see FIG. 4). From the results, it can be seen that, when human MSCs are treated with ET-1, a length of telomeres thereof may be extended to extend the lifespan of the stem cells, inhibit aging of the stem cells, and enhance growth and viability of the stem cells, which makes it possible to culture stem cells in a large scale in order to overcome conventional limitations in in vitro culture of human MSCs.

(11) Therefore, the present invention may provide a method for increasing stemness of human MSCs, which includes treating human MSCs with ET-1, and human MSCs having increased stemness using the method. Increasing the stemness of MSCs means that the MSCs have a high potential of differentiating into various mesoderm lineage cells such as bones, tendons, muscles, and the like. Accordingly, MSCs are expected to be a cell therapeutic agent applicable to a wider range of diseases. Also, the present invention may provide a composition for increasing stemness of human MSCs, which includes ET-1 as an active ingredient.

(12) In the present invention, the term cell culture broth refers to a culture broth of human MSCs. Here, the human MSCs may be derived from various tissues and pluripotent stem cells of human bodies, such as bone marrow, adipose tissues, cord blood, peripheral blood, neonatal tissues, human placenta, and the like. The human MSCs are preferably derived from bone marrow, but the present invention is not limited thereto.

(13) In the present invention, the term stem cell refers to a cell that may differentiate into various cells constituting biological tissues, and thus generally includes undifferentiated cells that may be regenerated in an unrestricted manner to form specialized cells in tissues and organs. The stem cells are developmental pluripotent or multipotent cells. The stem cells may divide to produce two daughter stem cells or produce one daughter stem cell and one progenitor (transit) cell, which then proliferate into fully differentiated and mature cells in tissues.

(14) The term cell culture broth used in the present invention refers to a medium containing cultured cells, and the term medium refers to a medium for animal cells generally used in the related art. Any medium generally used for animal cell culture may be used as the medium that may be used in the present invention. For example, an Eagle's minimum essential medium (MEM) (Eagle, H. Science 130: 432 (1959)), -MEM (Stanner, C. P. et al., Nat. New Biol. 230: 52 (1971)), Iscove's MEM (Iscove, N. et al., J. Exp. Med. 147: 923 (1978)), Medium 199 (Morgan et al., Proc. Soc. Exp. Bio. Med., 73: 1 (1950)), CMRL 1066, RPMI 1640 (Moore et al., J. Amer. Med. Assoc. 199: 519 (1967)), F12 (Ham, Proc. Natl. Acad. Sci. USA 53: 288 (1965)), F10 (Ham, R. G. Exp. Cell Res. 29: 515 (1963)), a Dulbecco's modification of Eagle's medium (DMEM: Dulbecco, R. et al., Virology 8: 396 (1959)), a mixture of DMEM and F12 (Barnes, D. et al., Anal. Biochem. 102: 255 (1980)), Way-mouth's MB752/1 (Waymouth, C. J. Natl. Cancer Inst. 22: 1003 (1959)), McCoy's 5A (McCoy, T. A., et al., Proc. Soc. Exp. Biol. Med. 100: 115 (1959)), MCDB series (Ham, R. G. et al., In Vitro 14: 11 (1978)), and the like may be used. Therefore, the medium may be preferably selected from the group consisting of -MEM, Eagles's MEM, Iscove's MEM, Medium 199, CMRL 1066, RPMI 1640, F12, F10, DMEM, Way-mouth's MB752/1, and McCoy's 5A. Most preferably, the medium may be an -MEM medium, but the present invention is not limited thereto. The medium of the present invention may further include a serum. In addition to the serum, the medium of the present invention may include any components known in the related art for a conventional composition for culturing stem cells to effectively culture the stem cells.

(15) Also, in the present invention, ET-1 is preferably included in the medium at a concentration of 0.0125 to 0.25 g/mL, is more preferably included in the medium at a concentration of 0.02 to 0.09 g/mL, and is most preferably included in the medium at a concentration of 0.02 to 0.03 g/mL, but the present invention is not limited thereto.

(16) Hereinafter, preferred examples are provided to aid in understanding the present invention. However, it should be understood that detailed description provided herein is merely intended to provide a better understanding of the present invention and is not intended to limit the scope of the present invention.

EXAMPLES

Example 1: Confirmation of Effect of ET-1 Treatment on Increase in Stemness of Human MSCs

(17) To check whether ET-1 increased stemness of human MSCs, expression of the most common marker Oct4 as a stemness-related factor was examined.

(18) 1-1. Confirmation of Western Blotting Results

(19) To determine a level of expression of an Oct4 protein in human MSCs when the human MSCs were treated with ET-1, human MSCs purchased from Lonza were treated with an increasing concentration (0, 0.0125, 0.025, 0.125, and 0.25 g/mL) of ET-1, and a level of protein expression was determined through western blotting. In this case, types of primary and secondary antibodies used and a dilution ratio thereof are listed in the following Table 1.

(20) TABLE-US-00001 TABLE 1 Primary Protein Size (kDa) Antibody Secondary Antibody ECL Oct4 43 Santacruz anti- Anti-goat IgG (whole Approximately Oct4 antibody molecule)-peroxidase 7 minutes sc-9081 antibody produced in rabbit 1:2,000 Dilution (Sigma-Aldrich A5420) 1:3,000 dilution Positive 55 1:10,000 Anti-mouse IgG (whole Approximately control (- Dilution molecule)-peroxidase 5 seconds tubulin) antibody produced in goat (Sigma-Aldrich A4416) 1:23,000 dilution

(21) As a result, it can be seen that the level of protein expression of the stemness marker Oct4 was significantly increased when the human MSCs were treated with ET-1, particularly the Oct4 had the highest level of protein expression when the human MSCs were treated with ET-1 at a concentration of 0.025 g/mL, as shown in FIG. 1

(22) 1-2. Confirmation of Real Time PCR Results

(23) To compare levels of mRNA expression of Oct4 in human MSCs treated with ET-1, the human MSCs were treated with ET-1, and RNA was extracted therefrom after 24 hours to synthesize complementary cDNA. Thereafter, real time PCR was performed using the complementary cDNA as a template and Oct4 amplification primers set forth in the following SEQ ID NOs: 1 and 2.

(24) SEQ ID NO: 1: 5-gaggcaacct ggagaatttg-3 (Oct4 forward primer)

(25) SEQ ID NO: 2: 5-tagcctgggg taccaaaatg-3 (Oct4 reverse primer)

(26) As a result, it was confirmed that the mRNA expression of Oct4 increased when the human MSCs were treated with ET-1, as shown in FIG. 2.

Example 2: Confirmation of Change in Length of Telomeres in Human MSCs Through ET-1 Treatment

(27) To check a change in a length of telomeres in human MSCs when the human MSCs were treated or were not treated with ET-1, the human MSCs were prepared so that the cells reached a confluency of 60% on a 60 mm plate. Before the human MSCs were treated with ET-1, a culture broth was replaced with a fresh culture broth. Thereafter, the human MSCs were treated with 0.025 g/mL of ET-1, and the medium was replaced with a fresh culture broth after 24 hours. After 3 days, gDNA samples were collected. Then, real time gDNA PCR was performed using the samples to compare the lengths of the telomeres by means of ET-1 treatment.

(28) As a result, it was confirmed that the lengths of the telomeres were extended approximately three-fold or more when the human MSCs were treated with ET-1, as shown in FIG. 3.

Example 3: Confirmation of Chromosomal Stability in Human MSCs Treated with ET-1

(29) Because the lengths of the telomeres were extended when the human MSCs from Example 2 were treated with ET-1, chromosomal stability thereof was checked using a G-banding karyotype analysis method in which chromosomal dysfunction was not induced. For this purpose, the G-banding karyotype analysis method known as a basic test method for evaluating genomic stability was performed. The G-banding karyotype analysis method is a method of pre-treating stem cells with trypsin, which is a proteolytic enzyme, and staining chromosomes with a Giemsa stain. In this case, euchromatin is stained with a light color, and heterochromatin is stained with a dark color. The G-banding karyotype analysis method is the test method most often used for chromosomal analysis because many staining bands are generated.

(30) As a result of the G-banding karyotype analysis, it was confirmed that chromosomal dysfunction was not induced when the human MSCs were treated with ET-1, as shown in FIG. 4.

(31) Although the present invention presented herein has been disclosed for illustrative purposes, it should be apparent to those skilled in the art to which the present invention belongs that various modifications and changes are possible without departing from the scope and spirit of the present invention. Therefore, it should be understood that the exemplary embodiments disclosed above are illustrative in all aspects and are not intended to limit the present invention.