參考文獻 |
1. Thomson, J.A., et al., Embryonic stem cell lines derived from human blastocysts. Science, 1998. 282(5391): p. 1145-1147.
2. Jiang, Y., et al., Pluripotency of mesenchymal stem cells derived from adult marrow (vol 418, pg 41, 2002). Nature, 2007. 447(7146): p. 879-880.
3. Higuchi, A., et al., Biomimetic Cell Culture Proteins as Extracellular Matrices for Stem Cell Differentiation. Chemical Reviews, 2012. 112(8): p. 4507-4540.
4. Okita, K., T. Ichisaka, and S. Yamanaka, Generation of germline-competent induced pluripotent stem cells. Nature, 2007. 448(7151): p. 313-U1.
5. Takahashi, K. and S. Yamanaka, Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell, 2006. 126(4): p. 663-676.
6. Yu, J., et al., Induced pluripotent stem cell lines derived from human somatic cells. Science, 2007. 318(5858): p. 1917-1920.
7. Lin, S.-L., et al., Mir-302 reprograms human skin cancer cells into a pluripotent ES-cell-like state. Rna-a Publication of the Rna Society, 2008. 14(10): p. 2115-2124.
8. Zhou, H., et al., Generation of Induced Pluripotent Stem Cells Using Recombinant Proteins. Cell Stem Cell, 2009. 4(5): p. 381-384.
9. Higuchi, A., et al., Biomaterials for the Feeder-Free Culture of Human Embryonic Stem Cells and Induced Pluripotent Stem Cells. Chemical Reviews, 2011. 111(5): p. 3021-3035.
10. Bosi, A. and B. Bartolozzi, Safety of Bone Marrow Stem Cell Donation: A Review. Transplantation Proceedings, 2010. 42(6): p. 2192-2194.
11. Favre, G., et al., Differences between graft product and donor side effects following bone marrow or stem cell donation. Bone Marrow Transplantation, 2003. 32(9): p. 873-880.
12. Gratwohl, A., et al., Predictability of hematopoietic stem cell transplantation rates. Haematologica-the Hematology Journal, 2007. 92(12): p. 1679-1686.
13. Hamidieh, A.A., et al., Autologous Stem Cell Transplantation as Treatment Modality in a Patient With Relapsed Pancreatoblastoma. Pediatric Blood & Cancer, 2010. 55(3): p. 573-576.
14. Higuchi, A., et al., Separation of hematopoietic stem cells from human peripheral blood through modified polyurethane foaming membranes. Journal of Biomedical Materials Research Part A, 2008. 85a(4): p. 853-861.
15. Arinzeh, T.L., et al., Allogeneic mesenchymal stem cells regenerate bone in a critical-sized canine segmental defect. Journal of Bone and Joint Surgery-American Volume, 2003. 85a(10): p. 1927-1935.
16. Caplan, A.I. and J.E. Dennis, Mesenchymal stem cells as trophic mediators. Journal of Cellular Biochemistry, 2006. 98(5): p. 1076-1084.
17. Horwitz, E.M., et al., Isolated allogeneic bone marrow-derived mesenchymal cells engraft and stimulate growth in children with osteogenesis imperfecta: Implications for cell therapy of bone. Proceedings of the National Academy of Sciences of the United States of America, 2002. 99(13): p. 8932-8937.
18. Pittenger, M.F., et al., Multilineage potential of adult human mesenchymal stem cells. Science, 1999. 284(5411): p. 143-147.
19. Scadden, D.T., The stem-cell niche as an entity of action. Nature, 2006. 441(7097): p. 1075-1079.
20. Kern, S., et al., Comparative analysis of mesenchymal stem cells from bone marrow, umbilical cord blood, or adipose tissue. Stem Cells, 2006. 24(5): p. 1294-1301.
21. Crisan, M., et al., A perivascular origin for mesenchymal stem cells in multiple human organs. Cell Stem Cell, 2008. 3(3): p. 301-313.
22. Brighton, C.T. and R.M. Hunt, EARLY HISTOLOGICAL AND ULTRASTRUCTURAL-CHANGES IN MEDULLARY FRACTURE CALLUS. Journal of Bone and Joint Surgery-American Volume, 1991. 73A(6): p. 832-847.
23. Netter, F.H., Musculoskeletal System: Anatomy, physiology and metabolic disorders. U.S.A : Indoo, 1987.
24. Zuk, P.A., et al., Multilineage cells from human adipose tissue: Implications for cell-based therapies. Tissue Engineering, 2001. 7(2): p. 211-228.
25. Aust, L., et al., Yield of human adipose-derived adult stem cells from liposuction aspirates. Cytotherapy, 2004. 6(1): p. 7-14.
26. Gimble, J.M. and F. Guilak, Differentiation potential of adipose derived adult stem (ADAS) cells. Current Topics in Developmental Biology, Vol 58, 2003. 58: p. 137-160.
27. Fraser, J.K., et al., Fat tissue: an underappreciated source of stem cells for biotechnology. Trends in Biotechnology, 2006. 24(4): p. 150-154.
28. Locke, M., J. Windsor, and P.R. Dunbar, Human adipose-derived stem cells: isolation, characterization and applications in surgery. Anz Journal of Surgery, 2009. 79(4): p. 235-244.
29. Zuk, P.A., et al., Human adipose tissue is a source of multipotent stem cells. Molecular Biology of the Cell, 2002. 13(12): p. 4279-4295.
30. van Dijk, A., et al., Differentiation of human adipose-derived stem cells towards cardiomyocytes is facilitated by laminin. Cell and Tissue Research, 2008. 334(3): p. 457-467.
31. Schaeffler, A. and C. Buechler, Concise review: Adipose tissue-derived stromal cells - Basic and clinical implications for novel cell-based therapies. Stem Cells, 2007. 25(4): p. 818-827.
32. Mitchell, J.B., et al., Immunophenotype of human adipose-derived cells: Temporal changes in stromal-associated and stem cell-associated markers. Stem Cells, 2006. 24(2): p. 376-385.
33. Oedayrajsingh-Varma, M.J., et al., Adipose tissue-derived mesenchymal stem cell yield and growth characteristics are affected by the tissue-harvesting procedure. Cytotherapy, 2006. 8(2): p. 166-177.
34. Zaragosi, L.-E., G. Ailhaud, and C. Dani, Autocrine fibroblast growth factor 2 signaling is critical for self-renewal of human multipotent adipose-derived stem cells. Stem Cells, 2006. 24(11): p. 2412-2419.
35. Rubio, D., et al., Spontaneous human adult stem cell transformation (Retracted article. See vol. 70, pg. 6682, 2010). Cancer Research, 2005. 65(8): p. 3035-3039.
36. Liu, Q., et al., A comparative study of proliferation and osteogenic differentiation of adipose-derived stem cells on akermanite and beta-TCP ceramics. Biomaterials, 2008. 29(36): p. 4792-4799.
37. Ahn, H.H., et al., In Vivo Osteogenic Differentiation of Human Adipose-Derived Stem Cells in an Injectable In Situ-Forming Gel Scaffold. Tissue Engineering Part A, 2009. 15(7): p. 1821-1832.
38. Flynn, L.E., The use of decellularized adipose tissue to provide an inductive microenvironment for the adipogenic differentiation of human adipose-derived stem cells. Biomaterials, 2010. 31(17): p. 4715-4724.
39. Natesan, S., et al., Adipose-Derived Stem Cell Delivery into Collagen Gels Using Chitosan Microspheres. Tissue Engineering Part A, 2010. 16(4): p. 1369-1384.
40. Awad, H.A., et al., Chondrogenic differentiation of adipose-derived adult stem cells in agarose, alginate, and gelatin scaffolds. Biomaterials, 2004. 25(16): p. 3211-3222.
41. Betre, H., et al., Chondrocytic differentiation of human adipose-derived adult stem cells in elastin-like polypeptide. Biomaterials, 2006. 27(1): p. 91-99.
42. Tchkonia, T., et al., Abundance of two human preadipocyte subtypes with distinct capacities for replication, adipogenesis, and apoptosis varies among fat depots. American Journal of Physiology-Endocrinology and Metabolism, 2005. 288(1): p. E267-E277.
43. Tchkonia, T., et al., Fat depot-specific characteristics are retained in strains derived from single human preadipocytes. Diabetes, 2006. 55(9): p. 2571-2578.
44. Macotela, Y., et al., Intrinsic Differences in Adipocyte Precursor Cells From Different White Fat Depots. Diabetes, 2012. 61(7): p. 1691-1699.
45. Shi, Y.Y., et al., The osteogenic potential of adipose-derived mesenchymal cells is maintained with aging. Plastic and Reconstructive Surgery, 2005. 116(6): p. 1686-1696.
46. Rider, D.A., et al., Autocrine fibroblast growth factor 2 increases the multipotentiality of human adipose-derived mesenchymal stem cells. Stem Cells, 2008. 26(6): p. 1598-1608.
47. Peptan, I.A., L. Hong, and J.J. Mao, Comparison of osteogenic potentials of visceral and subcutaneous adipose-derived cells of rabbits. Plastic and Reconstructive Surgery, 2006. 117(5): p. 1462-1470.
48. Mochizuki, T., et al., Higher chondrogenic potential of fibrous synovium- and adipose synovium-derived cells compared with. subcutaneous fat-derived cells - Distinguishing properties of mesenchymal stem cells in humans. Arthritis and Rheumatism, 2006. 54(3): p. 843-853.
49. Stein, G.S., et al., Transcriptional control of osteoblast growth and differentiation. Physiological Reviews, 1996. 76(2): p. 593-629.
50. Martin, I., et al., Selective differentiation of mammalian bone marrow stromal cells cultured on three-dimensional polymer foams. Journal of Biomedical Materials Research, 2001. 55(2): p. 229-235.
51. Noeth, U., et al., Chondrogenic differentiation of human mesenchymal stem cells in collagen type I hydrogels. Journal of Biomedical Materials Research Part A, 2007. 83A(3): p. 626-635.
52. Miyahara, Y., et al., Monolayered mesenchymal stem cells repair scarred myocardium after myocardial infarction. Nature Medicine, 2006. 12(4): p. 459-465.
53. Planat-Benard, V., et al., Spontaneous cardiomyocyte differentiation from adipose tissue stroma cells. Circulation Research, 2004. 94(2): p. 223-229.
54. Strem, B.M., et al., Expression of cardiomyocytic markers on adipose tissue-derived cells in a murine model of acute myocardial injury. Cytotherapy, 2005. 7(3): p. 282-291.
55. Rodriguez, A.M., et al., Transplantation of a multipotent cell population from human adipose tissue induces dystrophin expression in the immunocompetent mdx mouse. Journal of Experimental Medicine, 2005. 201(9): p. 1397-1405.
56. Sefcik, L.S., et al., Collagen nanofibres are a biomimetic substrate for the serum-free osteogenic differentiation of human adipose stem cells. Journal of Tissue Engineering and Regenerative Medicine, 2008. 2(4): p. 210-220.
57. Malafaya, P.B., et al., Chitosan particles agglomerated scaffolds for cartilage and osteochondral tissue engineering approaches with adipose tissue derived stem cells. Journal of Materials Science-Materials in Medicine, 2005. 16(12): p. 1077-1085.
58. Engler, A.J., et al., Matrix elasticity directs stem cell lineage specification. Cell, 2006. 126(4): p. 677-689.
59. Ward, D.F., Jr., et al., Mechanical strain enhances extracellular matrix-induced gene focusing and promotes osteogenic differentiation of human mesenchymal stem cells through an extracellular-related kinase-dependent pathway. Stem Cells and Development, 2007. 16(3): p. 467-479.
60. Zscharnack, M., et al., Low Oxygen Expansion Improves Subsequent Chondrogenesis of Ovine Bone-Marrow-Derived Mesenchymal Stem Cells in Collagen Type I Hydrogel. Cells Tissues Organs, 2009. 190(2): p. 81-93.
61. Zimmerlin, L., et al., Stromal Vascular Progenitors in Adult Human Adipose Tissue. Cytometry Part A, 2010. 77A(1): p. 22-30.
62. Yoshimura, K., et al., Characterization of freshly isolated and cultured cells derived from the fatty and fluid portions of liposuction aspirates. Journal of Cellular Physiology, 2006. 208(1): p. 64-76.
63. Civin CI, S.L., Brovall C, Fackler MJ, Schwartz JF, Shaper JH., Antigenic analysis of hematopoiesis. III. A hematopoietic progenitor cell surface antigen defined by a monoclonal antibody raised against KG-1a cells. J Immunol, 1984. 133(1): p. 157-65.
64. Asahara, T., et al., Isolation of putative progenitor endothelial cells for angiogenesis. Science, 1997. 275(5302): p. 964-967.
65. Pusztaszeri, M.P., W. Seelentag, and F.T. Bosman, Immunohistochemical expression of endothelial markers CD31, CD34, von Willebrand factor, and Fli-1 in normal human tissues. Journal of Histochemistry & Cytochemistry, 2006. 54(4): p. 385-395.
66. Lin, G., et al., Defining Stem and Progenitor Cells within Adipose Tissue. Stem Cells and Development, 2008. 17(6): p. 1053-1063.
67. Traktuev, D.O., et al., A population of multipotent CD34-positive adipose stromal cells share pericyte and mesenchymal surface markers, reside in a periendothelial location, and stabilize endothelial networks. Circulation Research, 2008. 102(1): p. 77-85.
68. Zannettino, A.C.W., et al., Multipotential human adipose-derived stromal stem cells exhibit a perivascular phenotype in vitro and in vivo. Journal of Cellular Physiology, 2008. 214(2): p. 413-421.
69. Sengenes, C., et al., Preadipocytes in the human subcutaneous adipose tissue display distinct features from the adult mesenchymal and hematopoietic stem cells. Journal of Cellular Physiology, 2005. 205(1): p. 114-122.
70. Mizuno, H., M. Tobita, and A.C. Uysal, Concise Review: Adipose-Derived Stem Cells as a Novel Tool for Future Regenerative Medicine. Stem Cells, 2012. 30(5): p. 804-810.
71. Higuchi, A., et al., Cell separation between mesenchymal progenitor cells through porous polymeric membranes. Journal of Biomedical Materials Research Part B-Applied Biomaterials, 2005. 74B(1): p. 511-519.
72. Higuchi, A., et al., Separation of CD34(+) cells from human peripheral blood through polyurethane foaming membranes. Journal of Biomedical Materials Research Part A, 2006. 78A(3): p. 491-499.
73. Rodbell, M., Metabolism of isolated fat cells. II. The similar effects of phospholipase C (Clostridium perfringens alpha toxin) and of insulin on glucose and amino acid metabolism. J Biol Chem, 1966. 241(1): p. 130-9.
74. Rodbell, M., The metabolism of isolated fat cells. IV. Regulation of release of protein by lipolytic hormones and insulin. J Biol Chem, 1966. 241(17): p. 3909-17.
75. Rodbell, M.a.A.B.J., Metabolism of isolated fat cells. 3. The similar inhibitory action of phospholipase C (Clostridium perfringens alpha toxin) and of insulin on lipolysis stimulated by lipolytic hormones and theophylline. J Biol Chem, 1966. 241(1): p. 140-2.
76. Kurita, M., et al., Influences of centrifugation on cells and tissues in liposuction aspirates: Optimized centrifugation for lipotransfer and cell isolation. Plastic and Reconstructive Surgery, 2008. 121(3): p. 1033-1041.
77. Higuchi, A., et al., Peripheral blood cell separation through surface-modified polyurethane membranes. Journal of Biomedical Materials Research Part A, 2004. 68A(1): p. 34-42.
78. Higuchi, A., et al., Separation of Hematopoietic Stem and Progenitor Cells from Human Peripheral Blood Through Polyurethane Foaming Membranes Modified with Several Amino Acids. Journal of Applied Polymer Science, 2009. 114(2): p. 671-679.
79. Chen, D.-C., et al., Purification of human adipose-derived stem cells from fat tissues using PLGA/silk screen hybrid membranes. Biomaterials, 2014. 35(14): p. 4278-4287.
80. McMurray, R.J., et al., Nanoscale surfaces for the long-term maintenance of mesenchymal stem cell phenotype and multipotency. Nature Materials, 2011. 10(8): p. 637-644.
81. Wu, C.-H., et al., The isolation and differentiation of human adipose-derived stem cells using membrane filtration. Biomaterials, 2012. 33(33): p. 8228-8239.
82. Higuchi, A., A hybrid-membrane migration method to isolate high-purity adipose-derived stem cells from fat tissues. Sci. Rep., 2015. 5(10217).
83. Fulwyler, M.J., Electronic separation of biological cells by volume. Science, 1965. 150(3698): p. 910-1.
84. Sweet, R.G., High Frequency Recording with Electrostatically Deflected Ink Jets. Review of Scientific Instruments, 1965. 36(2): p. 131-136.
85. Van Dilla, M.A., M.J. Fulwyler, and I.U. Boone, Volume Distribution and Separation of Normal Human Leucocytes. Experimental Biology and Medicine, 1967. 125(2): p. 367-370.
86. Bonner, W.A., et al., Fluorescence Activated Cell Sorting Review of Scientific Instruments, 1972. 43(3): p. 404-409.
87. Johnson, K.W., M. Doner, and P.J. Quesenberry, Flourescence Activated Cell Sorting: A Window on the Stem Cell Current Pharmaceutical Biotechnology 2007. 8(3): p. 133-139.
88. Assenmacher, M., et al., FLUORESCENCE-ACTIVATED CYTOMETRY CELL SORTING BASED ON IMMUNOLOGICAL RECOGNITION. Clinical Biochemistry, 1995. 28(1): p. 39-40.
89. Miltenyi, S.e.a., High gradient magnetic cell separation with MACS. Cytometry, 1990. 11(2): p. 231-238.
90. Kato, K.a.A.R., Isolation and Characterization of CD34+ hematopoietic stem cells from human peripheral blood by high-gradient magnetic cell sorting. Cytometry, 1993. 14(4): p. 384-392.
91. Dewynter, E.A., et al., COMPARISON OF PURITY AND ENRICHMENT OF CD34(+) CELLS FROM BONE-MARROW, UMBILICAL-CORD AND PERIPHERAL-BLOOD (PRIMED FOR APHERESIS) USING 5 SEPARATION SYSTEMS. Stem Cells, 1995. 13(5): p. 524-532.
92. McNiece, I., et al., Large-scale isolation of CD34+ cells using the Amgen Cell Selection Device results in high levels of purity and recovery. Journal of Hematotherapy, 1997. 6(1): p. 5-11.
93. Richel, D.J., et al., Highly purified CD34(+) cells isolated using magnetically activated cell selection provide rapid engraftment following high-dose chemotherapy in breast cancer patients. Bone Marrow Transplantation, 2000. 25(3): p. 243-249.
94. Ormerod, M.G., Flow cytometry: A practical approach, 3rd edition. Oxford University Press, 2000.
95. Watson, J., et al., Introduction to flow cytometry, First paperback edition. Cambridge University Press, 2004.
96. Olsen, B.R., A.M. Reginato, and W.F. Wang, Bone development. Annual Review of Cell and Developmental Biology, 2000. 16: p. 191-220.
97. Harada, S. and G.A. Rodan, Control of osteoblast function and regulation of bone mass. Nature, 2003. 423(6937): p. 349-355.
98. Lian, J.B., et al., Networks and hubs for the transcriptional control of osteoblastogenesis. Reviews in Endocrine & Metabolic Disorders, 2006. 7(1-2): p. 1-16.
99. Ducy, P., et al., Osf2/Cbfa1: A transcriptional activator of osteoblast differentiation. Cell, 1997. 89(5): p. 747-754.
100. Lengner, C.J., et al., Activation of the bone-related Runx2/Cbfa1 promoter in mesenchymal condensations and developing chondrocytes of the axial skeleton. Mechanisms of Development, 2002. 114(1-2): p. 167-170.
101. Romero-Prado, M., et al., Functional characterization of human mesenchymal stem cells that maintain osteochondral fates. Journal of Cellular Biochemistry, 2006. 98(6): p. 1457-1470.
102. Murtaugh, L.C., et al., The chick transcriptional repressor Nkx3.2 acts downstream of Shh to promote BMP-Dependent axial chondrogenesis. Developmental Cell, 2001. 1(3): p. 411-422.
103. Iwamoto, M., et al., Runx2 expression and action in chondrocytes are regulated by retinoid signaling and parathyroid hormone-related peptide (PTHrP). Osteoarthritis and Cartilage, 2003. 11(1): p. 6-15.
104. Eames, B.F., P.T. Sharpe, and J.A. Helms, Hierarchy revealed in the specification of three skeletal fates by Sox9 and Runx2. Developmental Biology, 2004. 274(1): p. 188-200.
105. Lengner, C.J., et al., Nkx3.2-mediated repression of Runx2 promotes chondrogenic differentiation. Journal of Biological Chemistry, 2005. 280(16): p. 15872-15879.
106. Guo, J., et al., PTH/PTHrP receptor delays chondrocyte hypertrophy via both Runx2-dependent and -independent pathways. Developmental Biology, 2006. 292(1): p. 116-128.
107. Provot, S., et al., Nkx3.2/Bapx1 acts as a negative regulator of chondrocyte maturation. Development, 2006. 133(4): p. 651-662.
108. Li, T.F., et al., Parathyroid hormone-related peptide (PTHrP) inhibits Runx2 expression through the PKA signaling pathway. Experimental Cell Research, 2004. 299(1): p. 128-136.
109. Zelzer, E., et al., Tissue specific regulation of VEGF expression during bone development requires Cbfa1/Runx2. Mechanisms of Development, 2001. 106(1-2): p. 97-106.
110. Pratap, J., et al., The Runx2 osteogenic transcription factor regulates matrix metalloproteinase 9 in bone metastatic cancer cells and controls cell invasion. Molecular and Cellular Biology, 2005. 25(19): p. 8581-8591.
111. ten Dijke, P., et al., Signal transduction of bone morphogenetic proteins in osteoblast differentiation. Journal of Bone and Joint Surgery-American Volume, 2003. 85A: p. 34-38.
112. Chen, D., M. Zhao, and G.R. Mundy, Bone morphogenetic proteins. Growth Factors, 2004. 22(4): p. 233-241.
113. Bidder, M., T. Latifi, and D.A. Towler, Reciprocal temporospatial patterns of Msx2 and osteocalcin gene expression during murine odontogenesis. Journal of Bone and Mineral Research, 1998. 13(4): p. 609-619.
114. Ferrari, D., et al., Dlx-5 in limb initiation in the chick embryo. Developmental Dynamics, 1999. 216(1): p. 10-15.
115. Holleville, N., et al., BMP signals regulate Dlx5 during early avian skull development. Developmental Biology, 2003. 257(1): p. 177-189.
116. Hassan, M.Q., et al., Dlx3 transcriptional regulation of osteoblast differentiation: Temporal recruitment of Msx2 Dlx3 an Dlx5 homeodomain proteins to chromatin of the osteocalcin gene. Molecular and Cellular Biology, 2004. 24(20): p. 9248-9261.
117. Depew, M.J., et al., Reassessing the Dlx code: the genetic regulation of branchial arch skeletal pattern and development. Journal of Anatomy, 2005. 207(5): p. 501-561.
118. Dodig, M., et al., Ectopic Msx2 overexpression inhibits and Msx2 antisense stimulates calvarial osteoblast differentiation. Developmental Biology, 1999. 209(2): p. 298-307.
119. Lee, M.H., et al., BMP-2-induced Runx2 expression is mediated by Dlx5, and TGF-beta 1 opposes the BMP-2-induced osteoblast differentiation by suppression of Dlx5 expression. Journal of Biological Chemistry, 2003. 278(36): p. 34387-34394.
120. Lee, M.H., et al., BMP-2-induced Osterix expression is mediated by Dlx5 but is independent of Runx2. Biochemical and Biophysical Research Communications, 2003. 309(3): p. 689-694.
121. Cheng, S.L., et al., Msx2 promotes osteogenesis and suppresses adipogenic differentiation of multipotent mesenchymal progenitors. Journal of Biological Chemistry, 2003. 278(46): p. 45969-45977.
122. Ichida, F., et al., Reciprocal roles of Msx2 in regulation of osteoblast and adipocyte differentiation. Journal of Biological Chemistry, 2004. 279(32): p. 34015-34022.
123. Yoshizawa, T., et al., Homeobox protein Msx2 acts as a molecular defense mechanism for preventing ossification in ligament fibroblasts. Molecular and Cellular Biology, 2004. 24(8): p. 3460-3472.
124. Balint, E., et al., Phenotype discovery by gene expression profiling: Mapping of biological processes linked to BMP-2-mediated osteoblast differentiation. Journal of Cellular Biochemistry, 2003. 89(2): p. 401-426.
125. Shirakabe, K., et al., Regulation of the activity of the transcription factor Runx2 by two homeobox proteins, Msx2 and Dlx5. Genes to Cells, 2001. 6(10): p. 851-856.
126. Hassan, M.Q.e.a., hoxa10: a BMP-2-responsive gene activates runx2 and regulates osteogenesis. Journal of Bone and Mineral Research, 2005. 20(9): p. S5-S5.
127. Lee, M.H., et al., Dlx5 specifically regulates Runx2 type II expression by binding to homeodomain-response elements in the Runx2 distal promoter. Journal of Biological Chemistry, 2005. 280(42): p. 35579-35587.
128. Nakashima, K., et al., The novel zinc finger-containing transcription factor Osterix is required for osteoblast differentiation and bone formation. Cell, 2002. 108(1): p. 17-29.
129. Pratap, J., et al., Cell growth regulatory role of Runx2 during proliferative expansion of preosteoblasts. Cancer Research, 2003. 63(17): p. 5357-5362.
130. Kim, Y.J., et al., The bone-related Zn finger transcription factor Osterix promotes proliferation of mesenchymal cells. Gene, 2006. 366(1): p. 145-151.
131. Selvamurugan, N., et al., Parathyroid hormone regulates the rat collagenase-3 promoter in osteoblastic cells through the cooperative interaction of the activator protein-1 site and the runt domain binding sequence. Journal of Biological Chemistry, 1998. 273(17): p. 10647-10657.
132. McCarthy, T.L., et al., Runt domain factor (Runx)-dependent effects on CCAAT/ enhancer-binding protein delta expression and activity in osteoblasts. J Biol Chem, 2000. 275(28): p. 21746-53.
133. Gutierrez, S., et al., CCAAT/enhancer-binding proteins (C/EBP) beta and delta activate osteocalcin gene transcription and synergize with Runx2 at the C/EBP element to regulate bone-specific expression. Journal of Biological Chemistry, 2002. 277(2): p. 1316-1323.
134. Xiao, G.Z., et al., Cooperative interactions between activating transcription factor 4 and Runx2/Cbfa1 stimulate osteoblast-specific osteocalcin gene expression. Journal of Biological Chemistry, 2005. 280(35): p. 30689-30696.
135. Yang, X.G., et al., ATF4 is a substrate of RSK2 and an essential regulator of osteoblast biology: Implication for Coffin-Lowry syndrome. Cell, 2004. 117(3): p. 387-398.
136. Otto, F., et al., Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development. Cell, 1997. 89(5): p. 765-771.
137. Komori, T., Regulation of osteoblast differentiation by transcription factors. Journal of Cellular Biochemistry, 2006. 99(5): p. 1233-1239.
138. Puchacz, E., et al., Chromosomal localization of the human osteocalcin gene. Endocrinology, 1989. 124(5): p. 2648-50.
139. Cancela, L., et al., MOLECULAR-STRUCTURE, CHROMOSOME ASSIGNMENT, AND PROMOTER ORGANIZATION OF THE HUMAN MATRIX GLA PROTEIN GENE. Journal of Biological Chemistry, 1990. 265(25): p. 15040-15048.
140. Lee, N.K., et al., Endocrine regulation of energy metabolism by the skeleton. Cell, 2007. 130(3): p. 456-469.
141. Nomura, S., et al., Developmental expression of 2ar (osteopontin) and SPARC (osteonectin) RNA as revealed by in situ hybridization. J Cell Biol, 1988. 106(2): p. 441-50.
142. Kuhn, K.e.a., The Structural Organization of Type IV Collagen Ann N Y Acad Sci, 1985. 460: p. 14-24.
143. Ashizawa, N., et al., Osteopontin is produced by rat cardiac fibroblasts and mediates A(II)-induced DNA synthesis and collagen gel contraction. Journal of Clinical Investigation, 1996. 98(10): p. 2218-2227.
144. Murry, C.E., et al., MACROPHAGES EXPRESS OSTEOPONTIN DURING REPAIR OF MYOCARDIAL NECROSIS. American Journal of Pathology, 1994. 145(6): p. 1450-1462.
145. Lkeda, T., et al., Osteopontin mRNA is expressed by smooth muscle-derived foam cells in human atherosclerotic lesions of the aorta. J Clin Invest 1993. 92(6): p. 2814-20.
146. Uaesoontrachoon, K., et al., Osteopontin and skeletal muscle myoblasts: Association with muscle regeneration and regulation of myoblast function in vitro. International Journal of Biochemistry & Cell Biology, 2008. 40(10): p. 2303-2314.
147. Merry, K., et al., Expression of osteopontin mRNA by osteoclasts and osteoblasts in modelling adult human bone. J Cell Sci, 1993. 104(Pt 4): p. 1013-20.
148. Choi, S.T., et al., Osteopontin might be involved in bone remodelling rather than in inflammation in ankylosing spondylitis. Rheumatology, 2008. 47(12): p. 1775-1779.
149. Reinholt, F.P., et al., OSTEOPONTIN - A POSSIBLE ANCHOR OF OSTEOCLASTS TO BONE. Proceedings of the National Academy of Sciences of the United States of America, 1990. 87(12): p. 4473-4475.
150. Donovan, P.J. and J. Gearhart, The end of the beginning for pluripotent stem cells. Nature, 2001. 414(6859): p. 92-97.
151. Rosner, M.H., et al., A POU-DOMAIN TRANSCRIPTION FACTOR IN EARLY STEM-CELLS AND GERM-CELLS OF THE MAMMALIAN EMBRYO. Nature, 1990. 345(6277): p. 686-692.
152. Carlin, R., et al., Expression of early transcription factors Oct-4, Sox-2 and Nanog by porcine umbilical cord (PUC) matrix cells. Reproductive Biology and Endocrinology, 2006. 4.
153. Chambers, I., et al., Functional expression cloning of Nanog, a pluripotency sustaining factor in embryonic stem cells. Cell, 2003. 113(5): p. 643-655.
154. Darr, H., Y. Mayshar, and N. Benvenisty, Overexpression of NANOG in human ES cells enables feeder-free growth while inducing primitive ectoderm features. Development, 2006. 133(6): p. 1193-1201.
155. Zaehres, H., et al., High-efficiency RNA interference in human embryonic stem cells. Stem Cells, 2005. 23(3): p. 299-305.
156. Chambers, I. and S.R. Tomlinson, The transcriptional foundation of pluripotency. Development, 2009. 136(14): p. 2311-2322.
157. Masui, S., et al., Pluripotency governed by Sox2 via regulation of Oct3/4 expression in mouse embryonic stem cells. Nature Cell Biology, 2007. 9(6): p. 625-U26.
158. Takeda, J., S. Seino, and G.I. Bell, HUMAN OCT3 GENE FAMILY - CDNA SEQUENCES, ALTERNATIVE SPLICING, GENE ORGANIZATION, CHROMOSOMAL LOCATION, AND EXPRESSION AT LOW-LEVELS IN ADULT TISSUES. Nucleic Acids Research, 1992. 20(17): p. 4613-4620.
159. Boyer, L.A., et al., Core transcriptional regulatory circuitry in human embryonic stem cells. Cell, 2005. 122(6): p. 947-956.
160. Looijenga, L.H.J., et al., POU5F1 (OCT3/4) identifies cells with pluripotent potential in human germ cell tumors. Cancer Research, 2003. 63(9): p. 2244-2250.
161. Rodda, D.J., et al., Transcriptional regulation of Nanog by Oct4 and Sox2. Journal of Biological Chemistry, 2005. 280(26): p. 24731-24737.
162. Ho, M.H., et al., Preparation of porous scaffolds by using freeze-extraction and freeze-gelation methods. Biomaterials, 2004. 25(1): p. 129-138.
163. Dai, W., et al., The influence of structural design of PLGA/collagen hybrid scaffolds in cartilage tissue engineering. Biomaterials, 2010. 31(8): p. 2141-2152.
164. Higuchi, A., et al., Differentiation ability of adipose-derived stem cells separated from adipose tissue by a membrane filtration method. Journal of Membrane Science, 2011. 366(1-2): p. 286-294.
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