The osteogenic potential of adipose-derived mesenchmal cells is maintained with aging

Plastic and Reconstructive Surgery

Volumn 116, Issue 6, 2005, Pages 1686-1696

  Shi, Yun Ying ^a,b   Nacamuli, Randall P ^a,b   Salim, Ali ^a,b   Longaker, Michael T ^a,b  

^a Stanford University School of Medicine ^*

^b STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALINE PHOSPHATASE; CALCIUM; CYCLINE; DYE; OIL RED O; UNCLASSIFIED DRUG;

ADIPOGENESIS; ADIPOSE DERIVED MESENCHYME CELL; ADIPOSE TISSUE; ADOLESCENT; AGED; AGING; ANIMAL CELL; ARTICLE; BONE DEVELOPMENT; BONE REGENERATION; CELL ADHESION; CELL DIFFERENTIATION; CELL PROLIFERATION; CELL THERAPY; EXTRACELLULAR CALCIUM; HISTOGENESIS; MESENCHYME CELL; MOUSE; MULTIPOTENT STEM CELL; NONHUMAN; PRIORITY JOURNAL; STAINING; THERAPY; VON KOSSA STAINING;

ADIPOSE TISSUE; AGING; ANIMALS; BLOTTING, WESTERN; CELL DIFFERENTIATION; CELLS, CULTURED; MESENCHYMAL STEM CELLS; MICE; OSTEOGENESIS; PROLIFERATING CELL NUCLEAR ANTIGEN;

EID: 23344443288     PISSN: 00321052     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.prs.0000185606.03222.a9     Document Type: Article

References (41)

1. Sirola, K. Regeneration of defects in the calvaria. Ann. Med. Exp. Biol. Fenn. 38: 1, 1960.
2. Aalami, O. O., Nacamuli, R. P., Lenton, K. A., et al. Applications of a mouse model of calvarial healing: Differences in regenerative abilities of juveniles and adults. Plast. Reconstr. Surg. 114: 713, 2004.
3. Cowan, C. M., Quarto, N., Warren, S. M., Salim, A., and Longaker, M. T. Age-related changes in the biomolecular mechanisms of calvarial osteoblast biology affect fibroblast growth factor-2 signaling and osteogenesis. J. Biol. Chem. 278: 32005, 2003.
4. Martinez, P., Esbrit, P., Rodrigo, A., Alvarez-Arroyo, M.V., and Martinez, M. E. Age-related changes in parathyroid hormone-related protein and vascular endothelial growth factor in human osteoblastic cells. Osteoporos. Int. 13: 874, 2002.
5. D'Avis, P. Y., Frazier, C. R., Shapiro, J. R., and Fedarko, N. S. Age-related changes in effects of insulin-like growth factor I on human osteoblast-like cells. Biochem. J. 324: 753, 1997.
6. Bergman, R. J., Gazit, D., Kahn, A. J., et al. Age-related changes in osteogenic stem cells in mice. J. Bone Miner. Res. 11: 568, 1996.
7. Stenderup, K., Justesen, J., Clausen, C., and Kassem, M. Aging is associated with decreased maximal life span and accelerated senescence of bone marrow stromal cells. Bone 33: 919, 2003.
8. Stenderup, K., Rosada, C., Justesen, J., et al. Aged human bone marrow stromal cells maintaining bone forming capacity in vivo evaluated using an improved method of visualization. Biogerontology 5: 107, 2004.
9. Mendes, S. C., Tibbe, J. M., Veenhof, M., et al. Bone tissue-engineered implants using human bone marrow stromal cells: Effect of culture conditions and donor age. Tissue Eng. 8: 911, 2002.
10. Huibregtse, B. A., Johnstone, B., Goldberg, V. M., and Caplan, A. I. Effect of age and sampling site on the chondro-osteogenic potential of rabbit marrow-derived mesenchymal progenitor cells. J. Orthop. Res. 18: 18, 2000.
11. Mueller, S. M., and Glowacki, J. Age-related decline in the osteogenic potential of human bone marrow cells cultured in three-dimensional collagen sponges. J. Cell. Biochem. 82: 583, 2001.
12. Zuk, P. A., Zhu, M., Mizuno, H., et al. Multilineage cells from human adipose tissue: Implications for cell-based therapies. Tissue Eng. 7: 211, 2001.
13. De Ugarte, D. A., Morizono, K., Elbarbary, A., et al. Comparison of multi-lineage cells from human adipose tissue and bone marrow. Cells Tissues Organs 174: 101, 2003.
14. Zuk, P. A., Zhu, M., Ashjian, P., et al. Human adipose tissue is a source of multipotent stem cells. Mol. Biol. Cell. 13: 4279, 2002.
15. Aust, L., Devlin, B., Foster, S. J., et al. Yield of human adipose-derived adult stem cells from liposuction aspirates. Cytotherapy 6: 7, 2004.
16. Safford, K. M., Hicok, K. C., Safford, S. D., et al. Neurogenic differentiation of murine and human adipose-derived stromal cells. Biochem. Biophys. Res. Commun. 294: 371, 2002.
17. Mizuno, H., Zuk, P. A., Zhu, M., et al. Myogenic differentiation by human processed lipoaspirate cells. Plast. Reconstr. Surg. 109: 199, 2002.
18. Erickson, G. R., Gimble, J. M., Franklin, D. M., et al. Chondrogenic potential of adipose tissue-derived stromal cells in vitro and in vivo. Biochem. Biophys. Res. Commun. 290: 763, 2002.
19. Halvorsen, Y. D., Franklin, D., Bond, A. L., et al. Extracellular matrix mineralization and osteoblast gene expression by human adipose tissue-derived stromal cells. Tissue Eng. 7: 729, 2001.
20. Huang, J. I., Beanes, S. R., Zhu, M., et al. Rat extramedullary adipose tissue as a source of osteochondrogenic progenitor cells. Plast. Reconstr. Surg. 109: 1033-1041; discussion 1042-1033, 2002.
21. Halvorsen, Y. D., Bond, A., Sen, A., et al. Thiazolidinediones and glucocorticoids synergistically induce differentiation of human adipose tissue stromal cells: Biochemical, cellular, and molecular analysis. Metabolism 50: 407, 2001.
22. Lee, J.A., Parrett, B. M., Conejero, J. A., et al. Biological alchemy: Engineering bone and fat from fat-derived stem cells. Ann. Plast. Surg. 50: 610, 2003.
23. Ogawa, R., Mizuno, H., Watanabe, A., et al. Osteogenic and chondrogenic differentiation by adipose-derived stem cells harvested from GFP transgenic mice. Biochem. Biophys. Res. Commun. 313: 871, 2004.
24. Hicok, K. C., Du Laney, T. V., Zhou, Y. S., et al. Human adipose-derived adult stem cells produce osteoid in vivo. Tissue Eng. 10: 371, 2004.
25. Cowan, C. M., Shi, Y. Y., Aalami, O. O., et al. Adipose-derived adult stromal cells heal critical-size mouse calvarial defects. Nat. Biotechnol. 22: 560, 2004.
26. Greenwald, J. A., Mehrara, B. J., Spector, J. A., et al. In vivo modulation of FGF biological activity alters cranial suture fate. Am. J. Pathol. 158: 441, 2001.
27. Mulliken, J. B., and Glowacki, J. Induced osteogenesis for repair and construction in the craniofacial region. Plast. Reconstr. Surg. 65: 553, 1980.
28. Bostrom, R., and Mikos, A. Tissue engineering of bone. In A. Atala, D. J. Mooney, J. P. Vacanti, and R. Langer (Eds.) Synthetic Biodegradable Polymer Scaffolds. Boston: Birkhauser, 1997. P. 215.
29. Pereira, R. F., Halford, K. W., and O'Hara, M. D. Cultured adherent cells from marrow can serve as long-lasting precursor cells for bone, cartilage, and lung in irradiated mice. Proc. Natl. Acad. Sci. U.S.A. 92: 4857, 1995.
30. Rezania, A., and Healy, K. E. Integrin subunits responsible for adhesion of human osteoblast-like cells to biomimetic peptide surfaces. J. Orthop. Res. 17: 615, 1999.
31. Carvalho, R. S., Schaffer, J. L., and Gerstenfeld, L. C. Osteoblasts induce osteopontin expression in response to attachment on fibronectin: Demonstration of a common role for integrin receptors in the signal transduction processes of cell attachment and mechanical stimulation. J. Cell. Biochem. 70: 376, 1998.
32. Vleminckx, K., and Kemler, R. Cadherins and tissue formation: Integrating adhesion and signaling. Bioessays 21: 211, 1999.
33. Suzawa, M., Takeuchi, Y., Fukumoto, S., et al. Extracellular matrix-associated bone morphogenetic proteins are essential for differentiation of murine osteoblastic cells in vitro. Endocrinology 140: 2125, 1999.
34. Lecanda, F., Avioli, L. V., and Cheng, S. L. Regulation of bone matrix protein expression and induction of differentiation of human osteoblasts and human bone marrow stromal cells by bone morphogenetic protein-2. J. Cell. Biochem. 67: 386, 1997.
35. Katagiri, T., Yamaguchi, A, Komaki, M., et al. Bone morphogenetic protein-2 converts the differentiation pathway of c2c12 myoblasts into the osteoblast lineage. J. Cell. Biol. 127: 1755, 1994.
36. Zhao, M., Harris, S. E., Horn, D., et al. Bone morphogenetic protein receptor signaling is necessary for normal murine postnatal bone formation. J. Cell. Biol. 157: 1049, 2002.
37. Khan, S. N., and Lane, J. M. The use of recombinant human bone morphogenetic protein-2 (rhbmp-2) in orthopaedic applications. Expert Opin. Biol. Ther. 4: 741, 2004.
38. Manji, S. S., Ng, K. W., Martin, T.J., and Zhou, H. Transcriptional and posttranscriptional regulation of osteopontin gene expression in preosteoblasts by retinoic acid. J. Cell. Physiol. 176: 1, 1998.
39. Iwamoto, M., Shapiro, I. M., Yagami, K., et al. Retinoic acid induces rapid mineralization and expression of mineralization-related genes in chondrocytes. Exp. Cell. Res. 207: 413, 1993.
40. Song, H. M., Nacamuli, R. P., Xia, W., et al. High-dose retinoic acid modulates rat calvarial osteoblast biology. J. Cell. Physiol. 202: 255, 2005.
41. Zuk, P. A. Personal communication, 2004.