Regulatory role of stromal cell-derived factor-1 in bone morphogenetic protein-2-induced chondrogenic differentiation in vitro

被引:30
作者
Guang, Liang G. [1 ]
Boskey, Adele L. [1 ,2 ]
Zhu, Wei [1 ,3 ]
机构
[1] Hosp Special Surg, Musculoskeletal Integr Program, New York, NY 10021 USA
[2] Weill Cornell Medial Coll, Dept Biochem, New York, NY 10021 USA
[3] Weill Cornell Medial Coll, Dept Cell & Dev Biol, New York, NY 10021 USA
关键词
Bone morphogenetic protein-2; Chondrogenic differentiation; C-X-C chemokine receptor-4; Mesenchymal progenitors; Stromal cell-derived factor-1; MESENCHYMAL STEM-CELLS; CHEMOKINE RECEPTOR CXCR4; CHONDROCYTE DIFFERENTIATION; OSTEOGENIC DIFFERENTIATION; TRANSCRIPTION FACTOR; CARTILAGE REPAIR; EXPRESSION; MATURATION; PROTEINS; MARROW;
D O I
10.1016/j.biocel.2012.06.033
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
Chemokine stromal cell-derived factor-1 (SDF-1) signals via binding to its primary transmembrane receptor, cysteine (C)-X-C chemokine receptor-4 (CXCR4). We previously reported that SDF-1 regulates osteogenic differentiation of mesenchymal stem/progenitor cells (MPCs) induced by bone morphogenetic protein-2 (BMP2). Although BMP2 is also capable of inducing chondrogenic differentiation of MPCs, the involvement of SDF-1 signaling in this function of BMP2 remains unknown. In this study, we aimed to test the role of SDF-1 signaling involved in BMP2-induced chondrogenic differentiation, using ATDC5 chondroprogenitors and mouse bone marrow-derived mesenchymal stromal cells (BMSCs). Our data showed that blocking of the SDF-1/CXCR4 pathway inhibits the differentiation of these cells into the chondrocytic lineages in response to BMP2 stimulation, evidenced by the reduced expression of type II collagen alpha 1 (Col2 alpha 1), aggrecan, and type X collagen alpha 1 (Col10 alpha 1), markers for chondrogenic differentiation. This effect of blocking SDF-1 signaling on BMP2-chondrogenic differentiation is associated with suppressed Sox9 and Runx2 expression (key transcription factors required for early and late stages of chondrogenic differentiation, respectively) and mediated via inhibiting intracellular Smad and Erk activation. Moreover, we found that addition of exogenous SDF-1 protein synergistically enhances the BMP2-induced chondrogenic differentiation in a dose-dependent manner. Collectively, our results demonstrated a novel role of SDF-1 signaling in regulating BMP2-induced chondrogenic differentiation in vitro. These data provide new insights into molecular mechanisms underlying BMP2-osteo/chondrogenesis, and may lead to the identification of new therapeutic targets and strategies to improve cartilage repair and regeneration in broad orthopaedic situations. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1825 / 1833
页数:9
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