Upregulation of Runx2 and Osterix during in vitro chondrogenesis of human adipose-derived stromal cells

被引:32
|
作者
Rich, Jason T. [6 ]
Rosova, Ivana [5 ]
Nolta, Jan A. [4 ]
Myckatyn, Terence M. [3 ]
Sandell, Linda J. [1 ,2 ]
McAlinden, Audrey [1 ,2 ]
机构
[1] Washington Univ, Sch Med, Dept Orthopaed Surg, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Div Plast & Reconstruct Surg, St Louis, MO 63110 USA
[4] Univ Calif Davis, Dept Internal Med, Stem Cell Program, Davis, CA 95616 USA
[5] Washington Univ, Sch Med, Dept Internal Med, St Louis, MO 63110 USA
[6] Washington Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, St Louis, MO 63110 USA
关键词
human adipose-derived stromal cells; (HADSC); mesenchymal stromal cell (MSC); mesenchymal stem cells; in vitro differentiation; chondrogenesis; TGF-beta; 3; transcription factors; Runx2; Osterix;
D O I
10.1016/j.bbrc.2008.05.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of this study was to create a gene expression profile to better define the phenotype of human adipose-derived stromal cells (HADSCs) during in vitro chondrogenesis, osteogenesis and adipogenesis. A novel aspect of this work was the analysis of the same subset of genes during HADSC differentiation into all three lineages. Chondrogenic induction resulted in increased mRNA expression of Sox transcription factors, COL2A1, COL10A1, Runx2, and Osterix. This is the first report demonstrating significant upregulation in expression of osteogenesis-related transcription factors Runx2 and Osterix by TGF-beta 3 induction of HADSCs during in vitro chondrogenesis. These findings suggest that the commonly-used chondrogenic induction reagents promote differentiation suggestive of hypertrophic chondrocytes and osteoblasts. We conclude that alternative strategies are required to induce efficient articular chondrocyte differentiation in order for HADSCs to be of clinical use in cartilage tissue engineering. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:230 / 235
页数:6
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