Functions of vitamin D, retinoic acid, and dexamethasone in mouse adipose-derived mesenchymal cells

被引:56
|
作者
Malladi, Preeti
Xu, Yue
Yang, George P.
Longaker, Michael T.
机构
[1] Stanford Univ, Sch Med, Pediat Surg Res Lab,Childrens Surg Res Program, Inst Stem Cell Biol & Regenerat Med,Dept Surg, Stanford, CA 94305 USA
[2] Palo Alto VA Hlth Care Syst, Palo Alto, CA USA
来源
TISSUE ENGINEERING | 2006年 / 12卷 / 07期
关键词
BONE-MARROW; STROMAL CELLS; STEM-CELLS; DIFFERENTIATION; TISSUE; GROWTH; ANALOG; OSTEOGENESIS; EXPRESSION; LEUKEMIA;
D O I
10.1089/ten.2006.12.2031
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Adipose-derived mesenchymal cells (AMCs) offer great promise for tissue engineering of bone. Previously, 1,25-dihydroxyvitamin D3, retinoic acid (RA), and dexamethasone had been shown to promote osteogenesis in bone marrow-derived mesenchymal cells (BMSCs). To study the osteogenic characteristics of mouse AMCs, we applied these 3 hormones alone and in combination to the AMCs and examined markers of osteogenic differentiation. Interestingly, vitamin D and RA demonstrated a consistent, dose-dependent enhancement of osteogenesis and upregulated osteoblast specific markers including osteopontin and osteocalcin. However, in AMCs, dexamethasone clearly inhibited osteogenic differentiation in a dose-dependent fashion and greatly increased the adipogenic marker peroxisome proliferator activated receptor gamma (PPARc). In summary, we show in vitro that vitamin D and RA are potential candidates to serve as enhancers of osteogenesis of AMCs and may be incorporated into future cell-based strategies for bone tissue engineering.
引用
收藏
页码:2031 / 2040
页数:10
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