OSTEOBLASTS DIFFERENTIATED FROM MESENCHYMAL STEM CELLS AND COMPOSITION FOR TREATING BONE DISEASE COMPRISING SAME

Abstract

The present invention relates to a method for differentiating mesenchymal stem cells into osteoblasts, a cell therapeutic agent for treating bone disease including osteoblasts differentiated by the method and a method for producing the same. In addition, the present invention relates to a method for treating bone disease, including the step of administering the osteoblasts obtained by the method to a patient with bone disease.

The differentiation method according to the present invention can stably and rapidly differentiate mesenchymal stem cells into osteoblasts. The differentiated osteoblasts have excellent blood vessel-forming ability and excellent bone-forming ability. Accordingly, the method for differentiating stem cells into osteoblasts and the osteoblasts obtained by the method, according to the present invention, can be effectively used as a cell therapeutic agent or treatment method related to bone disease.

Claims

1. A method for differentiating mesenchymal stem cells into osteoblasts, comprising the steps of: i) coating an air-permeable polymer membrane with surfactant bubbles; ii) inoculating mesenchymal stem cells into the bubbles of step i) at a density of 1×10.sup.3 to 1×10.sup.5 cells/cm.sup.2; iii) differentiating the mesenchymal stem cells of step ii) into osteoblasts in a differentiation medium; and iv) isolating and obtaining osteoblasts differentiated in step iii).

2. The method of claim 1, wherein the surfactant of step i) is a poloxamer.

3. The method of claim 1, wherein the bubbles of step i) are produced by comprising the step of: generating bubbles by adding a surfactant on the air-permeable polymer membrane and moving.

4. The method of claim 1, wherein the mesenchymal stem cells of step ii) are derived from any one or more selected from the group consisting of umbilical cord, umbilical cord blood, placenta, amniotic membrane, bone marrow, fat, hair follicle, tooth, pulp and skin dermis.

5. (canceled)

6. The method of claim 1, wherein the osteoblasts have higher expression levels of connexin 43 (CX43), Runt-related transcription factor 2 (RUNX2) and collagen type 1A1 (COL1A1) than undifferentiated stem cells and mature osteocytes; higher expression levels of angiopoietin 1 (ANGPT1) and alkaline phosphatase (AP) than undifferentiated stem cells; and lower expression levels of osterix (OSX), osteocalcin (OCN) and osteopontin (OPN) than mature osteocytes.

7. The method of claim 1, wherein the osteoblasts have a lower expression level of Ki-67 than undifferentiated stem cells.

8. A cell therapeutic agent for treating bone disease, comprising osteoblasts obtained by the method of claim 1.

9. The cell therapeutic agent of claim 8, wherein the osteoblasts have higher expression levels of connexin 43 (CX43), Runt-related transcription factor 2 (RUNX2) and collagen type 1A1 (COL1A1) than undifferentiated stem cells and mature osteocytes; higher expression levels of angiopoietin 1 (ANGPT1) and alkaline phosphatase (AP) than undifferentiated stem cells; and lower expression levels of osterix (OSX), osteocalcin (OCN) and osteopontin (OPN) than mature osteocytes.

10. The cell therapeutic agent of claim 8, wherein the osteoblasts have a lower expression level of Ki-67 than undifferentiated stem cells.

11. The cell therapeutic agent of claim 8, wherein the bone disease is any one or more selected from the group consisting of fracture, femoral head bone necrosis, spinal union, delayed union or nonunion, osteoporosis, osteonecrosis, pseudoarthrosis, Paget's disease and osteodystrophy.

12. A method for treating bone disease, comprising the step of: administering osteoblasts obtained by the method of claim 1 to a patient with bone disease.

Description

DESCRIPTION OF DRAWINGS

[0066] FIG. 1 shows a process for differentiating and obtaining umbilical cord-derived osteoblasts of the present invention.

[0067] FIG. 2 shows the results of observing for 7 hours (0H to 7H) whether the poloxamer solution was removed after the poloxamer bubble coating and the poloxamer bubbles remaining on the porous membrane were maintained. It was confirmed that the bubbles disappeared after 2 hours (2H) after the removal of the poloxamer solution.

[0068] FIG. 3 shows the results of loading QD-treated cells after poloxamer bubble coating, which was obtained by photographing as a 3D image under a fluorescence microscope.

[0069] FIG. 4 shows the cytotoxicity test results for each type of surfactant. As a result of day 1 of CCK-8 (cell counting kit-8), it was confirmed that the remaining surfactants (DIAPON K-SF and Tween-20) except for P407 (poloxamer 407) were toxic to cells.

[0070] FIG. 5 shows the cytotoxicity test results for each type of surfactant. As a result of confirming cell proliferation from day 1 to day 3 of CCK-8 (cell counting kit-8), it was confirmed that the remaining surfactants (DIAPON K-SF and Tween-20) except for P407 (poloxamer 407) were cytotoxic, and cells did not proliferate.

[0071] FIG. 6 shows the cytotoxicity test results for each type of surfactant. As a result of day 1 of CCK-8 (cell counting kit-8), it was confirmed that the remaining surfactants (methylprednisolone and Tween-20) except for P407 (poloxamer 407) were toxic to cells.

[0072] FIG. 7 shows the cytotoxicity test results for each type of surfactant. As a result of confirming cell proliferation from day 1 to day 3 of CCK-8 (cell counting kit-8), it was confirmed that the remaining surfactants (methylprednisolone and Tween-20) except for P407 (poloxamer 407) were cytotoxic, and cells did not proliferate.

[0073] FIG. 8 shows that the gene (COL1A) expression level of cells differentiated in a bubble foam surfactant was significantly higher than in undifferentiated cells or cells differentiated in gel surfactant.

[0074] FIG. 9 shows that the protein (VEGF) expression level of cells differentiated in a bubble foam surfactant was significantly higher than in undifferentiated cells or cells differentiated in a gel surfactant.

[0075] FIG. 10 shows the results of comparing the expression levels of the bone induction gene of the differentiated cell therapeutic agents (RCB001-DP1 to RCB005-DP5) of the present invention compared to the undifferentiated cells (RCB001, RCB002, RCB005). It was confirmed that the expression levels of connexin 43 (CX43) and Runt-related transcription factor 2 (RUNX2) secreted from the cell therapeutic agents of the present invention were significantly increased compared to undifferentiated cells.

[0076] FIG. 11 shows the results of comparing the expression levels of the bone inducing genes of the differentiated cell therapeutic agent (RCB005-DP1) of the present invention with bone marrow-derived mesenchymal stem cells (BM-MSC) and mature osteoblasts (NHOst) compared to the undifferentiated cells (RCB005). It was confirmed that the osteoblasts had higher expression levels of connexin 43 (CX43), Runt-related transcription factor 2 (RUNX2) and collagen type 1A1 (COL1A1) which are the early osteoblast markers, compared to the undifferentiated and mature osteoblasts, and the expression levels of osterix (OSX), osteocalcin (OCN) and osteopontin (OPN) were lower than those of the mature osteoblasts (NHOst).

[0077] FIG. 12 confirms that the osteogenic marker protein and the vascular inducing marker protein were increased in the differentiated osteocyte therapeutic agent of the present invention compared to the undifferentiated cells. (A) represents COL1A1, (B) represents Osteopontin (OPN), and (C) represents Angiopoietin.

[0078] FIG. 13 shows that the differentiated cell therapeutic agent of the present invention maintained the osteogenic marker protein and the vascular inducing marker protein even after day 3 to day 7 after thawing. (A) represents COL1A1, (B) represents osteopontin (OPN), and (C) represents angiopoietin.

[0079] FIG. 14 shows the vascular endothelial angiogenic ability of the umbilical cord-derived osteoblasts of the present invention. It was confirmed that, the umbilical cord-derived source cells (Undifferentiation UCMSC) and the osteogenic differentiation cell therapeutic agent were induced to produce blood vessels as much as the VEGF positive control known as the vascular angiogenic inducing factor, and in particular, the blood vessels formed by the proteins secreted by the cell therapeutic agent were formed to be thicker and stronger.

[0080] FIGS. 15a and 15b show the results of the effectiveness of the cell therapeutic agent of the present invention against a large animal (goat).

[0081] FIG. 16 shows the results of the effectiveness of the cell therapeutic agent of the present invention against a small animal (rat).

[0082] FIGS. 17a and 17b show the differentiation step from mesenchymal stem cells into osteocytes. The region indicated by the dotted line indicates the step of the cell therapeutic agent of the present invention.

[0083] FIG. 18 shows the results of confirming the cell mitogenic ability of the undifferentiated UCMSC (source) and the differentiated osteoblasts (DP) by Ki-67 (marker of cell division). Consistently, it was confirmed that the expression of Ki-67 rapidly decreased to 1% or less in DP, which means that CF-M801 is the osteoblasts in the early stage of the osteogenic model.

[0084] FIGS. 19a and 19b show the results of measuring CFU-F by using 2 batches of the undifferentiated stem cells BMMSC and UCMSC (source) and the differentiated osteoblasts (DP). It was confirmed that the CFU-F of the differentiated osteoblasts (DP, CF-M801) decreased in a pattern similar to the expression of Ki-67 (marker of cell division).

[0085] FIG. 20 shows the results of measuring the absorbance by staining with alkaline phosphatase after forming colonies by using 2 batches of the undifferentiated stem cells UCMSC (source) and the differentiated osteoblasts (DP). The colonies made by differentiated osteoblasts (DP) were stained with alkaline phosphatase and the absorbance value increased compared to undifferentiated cells, and thus, it was confirmed that the colonies produced by the proliferation of the present cell therapeutic agents were osteoblasts.

[0086] FIGS. 21a and 21b show that the differentiated osteoblasts (DP1 to DP3) of the present invention expressed 80% or more of CD10, whereas the undifferentiated mesenchymal stem cells expressed 15% or less of CD10. This means that the osteoblasts of the present invention were managed by checking the purity by confirming the osteoblast-specific markers, not the existing stem cell markers.

BEST MODE

Example 1

[0087] Isolation and Harvesting of Umbilical Cord-Derived Stem Cells

[0088] First, arterial and venous blood vessels were removed from a separated umbilical cord, and the remaining tissue was minced and reacted with AdiCol™ (CEFO) at 37° C. for 30 minutes or more, and then cells were extracted. The extracted cells were cultured in CEFOgro™ medium under conditions of 37° C. and 5% CO.sub.2 to obtain mesenchymal stem cells.

Example 2

[0089] Coating Air-Permeable Polymer Membrane with Surfactant Bubbles

[0090] On the porous membrane of a hyper flask, 8% poloxamer 407 dissolved in PBS was shaken to generate bubbles, and the remaining poloxamer solution was poured out. The air-permeable polymer membrane was coated with poloxamer bubbles at 37° C. for 2 hours. After removing the poloxamer 407 bubbles through microscopic 3D imaging, the solution was removed, and as a result of observing whether the bubbles were maintained, the bubbles started to disappear after 2 hours (2H), and after 5 hours (5H), it was confirmed that the bubbles completely disappeared (FIG. 2).

[0091] In addition, quantum dot-conjugated silica nanoparticles (QD) were uptaken into stem cells for 24 hours to track umbilical cord-derived mesenchymal stem cells. After the poloxamer 407 bubbles were generated, the solution was removed, and the cells were loaded and then imaged in 3D by using a microscope Z-stack (FIG. 3).

Example 3

[0092] Differentiation into Osteoblasts and Culture

[0093] After 2 hours after coating with poloxamer bubbles in [Example 2], the umbilical cord-derived stem cells obtained in [Example 1] were inoculated at a density of 1×10.sup.4 cells/cm.sup.2, and the cells were cultured in a culture medium including DMEM and FBS for 24 hours. The cultured stem cells were differentiated into osteoblasts for 72 hours in the bone differentiation medium.

Example 4

[0094] Selection of Suitable Surfactants for Coating Air-Permeable Polymer Membranes

[0095] The toxicity of poloxamer (poloxamer 407, p407), sodium methyl cocoyl taurate (DIAPON K-SF), polyoxyethylene sorbitan monolaurate (Tween 20) or methylprednisolone, which are known as representative biocompatible surfactants, was confirmed.

[0096] Specifically, in the upper chamber in a transwell including a three-dimensional porous membrane, the surfactant p407, DIAPON K-SF or Tween 20 was respectively treated at 0, 0.5 1, 5 or 15% (v/v) and coated for 2 hours in the same manner as in [Example 2], and then, the umbilical cord-derived mesenchymal stem cells obtained in [Example 1] were seeded at 20,000 cells/cm.sup.2. The cell growth medium was placed in the lower chamber and cultured for 3 days. On days 1, 2 and 3, the CCK-8 (Cat. CK04, DOJINDO) solution was added, and after 3 hours of reaction in a 37° C. CO.sub.2 incubator, absorbance was measured at 450 nm to analyze cytotoxicity (FIG. 4) and the degree of cell growth (FIG. 5).

[0097] Further, in a transwell including a three-dimensional porous membrane, the surfactant p407, methylprednisolone or Tween 20 was treated at a concentration of 4 mM in the upper chamber, and after coating for 2 hours in the same manner as in [Example 2], the umbilical cord-derived mesenchymal stem cells obtained in [Example 1] were seeded at 20,000 cell/cm.sup.2. The cell growth medium was placed in the lower chamber and cultured for 3 days. On days 1, 2 and 3, the CCK-8 solution was added, and after 3 hours of reaction in a 37° C. CO.sub.2 incubator, absorbance was measured at 450 nm to analyze cytotoxicity (FIG. 6) and the degree of cell growth (FIG. 7).

[0098] As a result, it was confirmed that all of the remaining DIAPON K-SF, Tween 20 and methylprednisolone except for P407 were toxic to cells, as shown in [FIG. 4] to [FIG. 7].

Example 5

[0099] Selection of Surfactant Coating Method

[0100] After coating poloxamer in a bubble or gel state on a hyper flask porous membrane, the degree of osteodifferentiation of umbilical cord-derived stem cells differentiated by the method of [Example 3] was compared.

[0101] Specifically, differentiation-induced osteoblasts and undifferentiated cells were respectively collected, treated with Trizol™ and chloroform (Sigma) and separated by centrifugation to obtain only mRNA. The obtained mRNA was synthesized as cDNA by using the Transcriptor Universal cDNA Master Kit (Roche). Thereafter, DNA was amplified through RT-PCR for COL1A1 to confirm the difference in the numbers of DNA copies at the gene level. Polymerase chain reaction conditions were 50 cycles of 95° C. for 10 seconds, 54° C. for 10 seconds and 72° C. for 30 seconds (FIG. 8).

[0102] In addition, by collecting the culture medium of osteoblasts and undifferentiated cells prepared and differentiated by the method of [Example 3], the degree of secretion of vascular endothelial growth factor (VEGF) was determined by performing enzyme-linked immunosorbent assay (ELISA) (FIG. 9).

[0103] As a result, as shown in [FIG. 8] and [FIG. 9], it was confirmed that the expression levels of osteoinduction genes and angiogenesis-inducing proteins in cells differentiated by the method of the present invention were more excellent than in cells differentiated from undifferentiated or gel-type poloxamer.

Example 6

[0104] Evaluation of Osteogenic Ability of Obtained Osteoblasts

[0105] <6-1> Osteogenic Ability of Osteoblasts (Gene Level)

[0106] After synthesizing cDNA by separating RNA from osteoblasts collected during the differentiation process of osteoblasts, the gene expression levels of Runt-related transcription factor 2 (RUNX2) and connexin 43 (CX43), which are osteogenic gene markers, were compared with those of undifferentiated cells by using real time-polymerase chain reaction (RT-PCR).

[0107] Specifically, osteoblasts and undifferentiated cells prepared and differentiated by the method of [Example 3] were respectively collected, treated with Trizol™ and chloroform (Sigma) and separated by centrifugation to obtain only mRNA. The obtained mRNA was synthesized as cDNA by using the Transcriptor Universal cDNA Master Kit (Roche). Thereafter, DNA was amplified through RT-PCR targeting RUNX2 and CX43 to determine the difference in expression levels at the gene level. Polymerase chain reaction conditions were 50 cycles of 95° C. for 10 seconds, 54° C. for 10 seconds and 72° C. for 30 seconds.

[0108] In addition, the mRNA was obtained by respectively collecting osteoblasts, undifferentiated cells, bone marrow-derived mesenchymal stem cells (BM-MSC) and mature osteocytes (NHOst) prepared and differentiated by the method of [Example 3], and the obtained mRNA was synthesized as cDNA by using the Transcriptor Universal cDNA Master Kit (Roche). Thereafter, DNA was amplified through RT-PCR for RUNX2, CX43 and COL1A to confirm the difference in expression levels at the gene level. Polymerase chain reaction conditions were 50 cycles of 95° C. for 10 seconds, 54° C. for 10 seconds and 72° C. for 30 seconds.

[0109] As a result, as shown in [FIG. 10] and [FIG. 11], it was confirmed that RUNX2, CX43 or COL1A was highly expressed in osteoblasts of the present invention compared to undifferentiated stem cells and mature osteocytes (NHOst). In [FIG. 10], RCB001, RCB002 and RCB005 refer to undifferentiated cells, and RCB001-DP1 to RCB005-DP5 refer to the differentiated cell therapeutic agents of the present invention.

[0110] On the other hand, OSX, OCN or OPN was expressed higher in mature osteoblasts (NHOst) than in the osteoblasts of the present invention, indicating that the osteoblasts of the present invention were in the immature osteodifferentiation stage compared to NHOst (FIG. 11). In [FIG. 11], RCB001, RCB002 and RCB005 refer to undifferentiated cells, and RCB001-DP1 to RCB005-DP5 refer to the differentiated cell therapeutic agents of the present invention.

[0111] <6-2> Osteogenesis Ability of Osteoblasts (Protein Level)

[0112] The change in the protein concentrations of collagen type 1A1 (COL1A), osteopontin or angiopoirtin (ANGPT-1), which are known as osteogenic or angiogenic protein markers, was confirmed in the culture medium and osteoblasts collected in the osteoblast differentiation process of [Example 3]. Additionally, it was attempted to determine whether the frozen cell therapeutic agent of the present invention could maintain bone morphogenetic proteins or vascular-inducing proteins even after thawing.

[0113] Specifically, the prepared and differentiation-induced osteoblasts, undifferentiated cells and the differentiation medium prepared and differentiated by the method of [Example 3] were respectively collected to perform enzyme-linked immunosorbent assay (ELISA). For COL1A, the degree of change in protein expression in the cells in which the cells were lysed was confirmed by taking differentiation-induced cells and undifferentiated cells, and for osteopontin and angiopoietin, the protein secretion levels were determined in the culture medium up to 72 hours of differentiation.

[0114] As a result, as shown in [FIG. 12], it was confirmed that the protein expression of COL1A was increased and the secretions of osteopontin and angiopoietin were all highly expressed in the osteoblasts of the present invention. In addition, as shown in [FIG. 13], it was confirmed that the bone-forming proteins or the vascular-inducing proteins of the cell therapeutic agent of the present invention was maintained even after 3 to 7 days after thawing. In [FIG. 12] and [FIG. 13], (A) denotes COL1A1, (B) denotes osteopontin (OPN) and (C) denotes angiopoietin.

Example 7

[0115] Evaluation of Angiogenic Ability of Obtained Osteoblasts

[0116] The angiogenic ability of human umbilical vein endothelial cells (HUVEC) due to the angiogenic protein secreted by the obtained osteoblasts was confirmed.

[0117] Specifically, undifferentiated stem cells or osteoblasts were inoculated at 4×10.sup.4 cells/well on a 12-well transwell plate including a porous membrane with 8.0 μm pore size, and quantum-dot was uptaken for 24 hours by using HUVEC cells in culture, and then, the cells were taken and inoculated at a density of 25,000/cm.sup.2 under the transwell. After inoculation, co-culture was carried out for 1 day to conduct the vascular tube formation analysis experiment for HUVEC. After seeding each cell in a 12-well plate, medium and substance exchange was allowed to occur by using a transwell, and then, the cells were cultured for 12 hours to confirm the vascular induction of HUVEC cells. Osteogenic differentiated cells and undifferentiated cells were placed on the transwell for comparison. The negative control group was inoculated with only HUVEC cells on the coated Matrigel and cultured for 12 hours by using the HUVEC medium without VEGF, and the positive control group was cultured with 20 ng/mL of VEGF added under the same conditions as the negative control group.

[0118] As a result, as shown in [FIG. 14], when co-cultured with umbilical cord-derived source cells (Undifferentiation UC-MSC) and the bone cell therapeutic agent to a similar level with the VEGF-positive control, which is known as an angiogenesis-inducing factor, it was confirmed that tube formation occurred. In addition, it was confirmed that thick and strong blood vessels were formed when co-cultured with the osteogenic differentiation cell therapeutic agent, and in particular, blood vessels formed by the protein secreted by the cell therapeutic agent were thicker and stronger.

Example 8

[0119] Confirmation of Bone Regeneration Ability of Obtained Osteoblasts—In Vivo

[0120] After inducing bone defects in a large animal (goat) or small animal (rat) model, it was attempted to determine the bone regeneration ability of the cell therapeutic agent of the present invention.

[0121] Specifically, after inducing a femoral bone defect in an immunosuppressed goat model, 1×10.sup.7 osteoblasts were treated per goat to confirm the bone regeneration effect for 26 weeks (Table 2). In addition, as an efficacy test for the goat model, bone tissue was demineralized for two and a half months, and histological evaluation of the efficacy of this cell therapeutic agent was carried out with H&E and Masson's Trichrome staining.

[0122] In the case of the immunosuppressed rat model, after inducing a radial bone defect, 1×10.sup.6 osteoblasts per rat were treated to confirm the effect of bone regeneration for 12 weeks (Table 3). The Sham control group was treated only with scaffolds composed of alginate. The degree of bone regeneration was confirmed by μCT image, and bone tissue was fixed, demineralized and sectioned to prepare slides, and after staining, new bone regeneration was confirmed.

TABLE-US-00002 TABLE 2 Number of Administered animals Group substance (M/F) Route Dose Sham control group — 6/6 Femoral — bone defect Test substance CF-M801 8/8 Femoral 1 × 10.sup.7 administration group bone defect

TABLE-US-00003 TABLE 3 Number of Administered animals Group substance (M/F) Route Dose Sham control group — 10 Radial — bone defect Test substance CF-M801 10 Radial 1 × 10.sup.6 administration group bone defect

[0123] As a result of the efficacy test for the goat model, as shown in [FIG. 15a] and [FIG. 15b], it was confirmed that in both males and females, the formation of new bone in the proximal and distal regions of the control group was very poor and only partially confirmed at 26 weeks, and it was confirmed that they were in the process of wound healing. On the other hand, in the proximal and distal parts of the cell-administered group, cells filled the defect site, proliferated and differentiated into osteocytes such that the new bone was well connected organically without breaking, and it was confirmed that the thickness was considerably increased (lower left white arrow in FIG. 15a). Blood vessels were also found to be well formed regularly. It was confirmed that the formation of new bone was significantly observed at both 13 and 26 weeks only in the cell-administered group.

[0124] As a result of the efficacy test on the rat model, as shown in [FIG. 16], the G3 group was a cell therapeutic agent group differentiated at passage 7 for 2 days, and the G5 group was a treatment group differentiated for 3 days at passage 5, and the volume of the bone, the volume density of bone and BMD tended to increase in both groups compared to the control group, and particularly, it was confirmed that the bone volume of the therapeutic agent group differentiated from passage 5 for 3 days increased more significantly.

Example 9

[0125] Confirmation of Stage of Cell Therapeutic Agent

[0126] It was intended to determine the stage of the cell therapeutic agent of the present invention.

[0127] <9-1> Confirmation of Ki-67 Expression

[0128] It is known that human Ki-67 is not expressed in the stationary phase (G0) of the cell cycle but is expressed in the proliferation phase (G1, S, G2, M phase), and the cell therapeutic agent is not expressed because cells do not differentiate after differentiating into osteocytes. Accordingly, in two batches of the undifferentiated UCMSC (source) and differentiated osteoblasts (DP) of the present invention, the expression level of Ki-67, which is an indicator of cell division, was confirmed by immunocytochemistry (ICC), and DAPI, which is a nuclear staining material, was stained to correct the expression level of Ki-67 compared to the number of cells.

[0129] Specifically, a slide plate was prepared, and undifferentiated and differentiated cells were inoculated into each well in 3×10.sup.5 doses, and then cultured in a CO.sub.2 incubator for 24 hours. Cells were fixed with 4% formaldehyde at room temperature for 10 minutes, and cells were permeabilized with 1% Triton X-100 for 10 minutes at room temperature. After blocking with BSA at room temperature for 30 minutes, the Ki-67 primary antibody was reacted at room temperature for 1 hour, and the fluorescence-linked secondary antibody was reacted at room temperature for 1 hour after blocking light. Mounting was performed by using ProLong™ Gold Antifade Mountant (Invitrogen) containing DAPI, and cells were observed by using a fluorescence microscope.

[0130] As a result, as shown in [FIG. 18], it was consistently confirmed that the expression of Ki-67 rapidly decreased to 1% or less in osteoblasts (DP).

[0131] <9-2> Confirmation of CFU-F Expression

[0132] CFU-F was measured by using two batches of undifferentiated stem cells BMMSC, UCMSC (source) and differentiated osteoblasts (DP) of the present invention. In addition, it is known that mesenchymal stem cells start to proliferate and form characteristic cell colonies when in vitro culture is started, and the cells in the colony look like fibroblasts, and each cell colony is called a colony forming unit-fibroblast, which is known as an important feature of stem cells. Accordingly, the formed colonies were observed with the naked eye and a camera photograph after 2% crystal violet staining was performed, and the dyed colonies were quantified by counting those with 3 mm or more and a density of 80% or more.

[0133] As a result, as shown in [FIG. 19a] and [FIG. 19b], it was confirmed that the CFU-F of the differentiated osteoblasts (DP, CF-M801) decreased in a pattern similar to the expression of Ki-67 (indicator of cell division) expression. In addition, it was confirmed that a large number of colonies were formed in bone marrow-derived stem cells and source cells, which are umbilical cord-derived stem cells, but almost no colony formation occurred in the cell therapeutic agent. From this, it was determined that the umbilical cord-derived stem cell source cells were differentiated into osteogenic differentiated cells, and thus lost the ability to form colonies. Through these results, it was confirmed that most of the cell therapeutic agents were differentiated from the source cells.

[0134] <9-3> Confirmation of ALP Expression

[0135] The purpose of this study was to determine whether the colony-forming cells, which appeared at an average of less than 1% in CFU-F using the cell therapeutic agent CF-M801, were undifferentiated mesenchymal stem cells or osteoblasts induced to differentiate.

[0136] Specifically, colonies that appeared after culturing in the same manner as CFU-F in Example <9-2> were stained with alkaline phosphatase (ALP) staining to determine whether or not bone differentiation occurred. After inoculating 10,000 cells and maintaining them for a week, ALP staining was performed. After ALP staining, dimethylsulfoxide was reacted to dissolve the stain, and only the supernatant was taken to measure the absorbance with a microplate reader.

[0137] As a result, as shown in [FIG. 20], undifferentiated UCMSCs, which are allogeneic umbilical cord-derived mesenchymal stem cells, showed little ALP staining, but osteodifferentiation-induced CF-M801 colonies were all ALP-positive in three different lots. In addition, the osteodifferentiation-induced CF-M801 showed higher absorbance compared to the undifferentiated cells. As a result of analyzing these by converting into relative values, it showed a value 1.5 times higher than that of undifferentiated UCMSC in all cases. As a result, it was confirmed that the differentiated osteoblasts (DP) were in a state where cell division did not stop for a certain period of time, and as the differentiation progressed, they gradually lost their dividing ability and differentiated into osteocytes.

[0138] In summary, the cell therapeutic agent of the present invention may differentiate mesenchymal stem cells into osteoblasts by RUNX2, which is a master regulator of osteocyte differentiation. It was found that early-stage osteoblasts (osteo-progenitors, immature osteoblasts) are RUNX2+, have proliferative capacity, differentiate into mature osteocytes, and further progress in mineralization (FIGS. 17a and 17b).

[0139] <9-4> Confirmation of CD-10 Expression

[0140] In order to confirm the differentiation of the cell therapeutic agents, the expression level of CD10 was determined by flow cytometry (FACS) and immunocytochemistry (ICC).

[0141] Specifically, osteoblasts, undifferentiated cells and bone marrow-derived mesenchymal stem cells (BM-MSC) prepared and differentiated by the method of [Example 3] were suspended in a 2% BSA/DPBS solution. The CD10 primary antibody was reacted at room temperature for 1 hour, and after washing, the FITC fluorescence-linked secondary antibody was reacted at room temperature for 30 minutes. After washing the cells, the supernatant was removed, 3.7% formaldehyde was added and fixed at room temperature for 20 minutes, and the expression level of CD10 was determined by using a flow cytometer (BD Accuri C6 Plus).

[0142] For ICC, a slide plate was prepared, and after inoculating undifferentiated and differentiated cells in 3×10.sup.5 doses in each well, the cells were cultured in a CO.sub.2 incubator for 24 hours. The cells were fixed with 4% formaldehyde at room temperature for 10 minutes, and the cells were permeabilized with 1% Triton X-100 for 10 minutes at room temperature. After blocking with BSA at room temperature for 30 minutes, the CD10 primary antibody was reacted at room temperature for 1 hour, and the FITC fluorescence-linked secondary antibody was reacted at room temperature for 1 hour after blocking light. Mounting was performed by using ProLong™ Gold Antifade Mountant (Invitrogen) containing DAPI, and the cells were observed using a fluorescence microscope.

[0143] As a result, as shown in [FIG. 21a] and [FIG. 21b], it was confirmed that the differentiated osteoblasts (DP1 to DP3) of the present invention expressed 80% or more of CD10, whereas the undifferentiated mesenchymal stem cells expressed 15% or less of CD10. This means that the osteoblasts of the present invention were managed by checking the purity by confirming the osteoblast-specific markers, not the existing stem cell markers.

INDUSTRIAL APPLICABILITY

[0144] The differentiation method according to the present invention can stably and rapidly differentiate mesenchymal stem cells into osteoblasts. The differentiated osteoblasts have excellent blood vessel-forming ability and excellent bone-forming ability. Accordingly, the method for differentiating stem cells into osteoblasts and the osteoblasts obtained by the method, according to the present invention, can be effectively used as a cell therapeutic agent or treatment method related to bone disease.