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维生素D、视黄酸和地塞米松在小鼠脂肪来源间充质细胞中的作用

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

作者信息

Malladi Preeti, Xu Yue, Yang George P, Longaker Michael T

机构信息

Children's Surgical Research Program, Department of Surgery, Stanford University School of Medicine, Stanford, California 94305, USA.

出版信息

Tissue Eng. 2006 Jul;12(7):2031-40. doi: 10.1089/ten.2006.12.2031.

Abstract

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 (PPAgamma). 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.

摘要

脂肪来源的间充质细胞(AMCs)在骨组织工程方面具有巨大潜力。此前,已证明1,25-二羟基维生素D3、视黄酸(RA)和地塞米松可促进骨髓来源的间充质细胞(BMSCs)的成骨作用。为了研究小鼠AMCs的成骨特性,我们将这三种激素单独及联合应用于AMCs,并检测成骨分化标志物。有趣的是,维生素D和RA表现出一致的、剂量依赖性的成骨增强作用,并上调了包括骨桥蛋白和骨钙素在内的成骨细胞特异性标志物。然而,在AMCs中,地塞米松以剂量依赖性方式明显抑制成骨分化,并显著增加脂肪生成标志物过氧化物酶体增殖物激活受体γ(PPAgamma)。总之,我们在体外表明,维生素D和RA是作为AMCs成骨增强剂的潜在候选物,可能会被纳入未来基于细胞的骨组织工程策略中。

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