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J Biol Chem ; 283(14): 9239-47, 2008 Apr 04.
Article in English | MEDLINE | ID: mdl-18276598

ABSTRACT

Adhesive signaling plays a key role in cellular differentiation, including in chondrogenesis. Herein, we probe the contribution to early chondrogenesis of two key modulators of adhesion, namely focal adhesion kinase (FAK)/Src and CCN2 (connective tissue growth factor, CTGF). We use the micromass model of chondrogenesis to show that FAK/Src signaling, which mediates cell/matrix attachment, suppresses early chondrogenesis, including the induction of Ccn2, Agc, and Sox6. The FAK/Src inhibitor PP2 elevates Ccn2, Agc, and Sox6 expression in wild-type mesenchymal cells in micromass culture, but not in cells lacking CCN2. Our results suggest a reduction in FAK/Src signaling is a critical feature permitting chondrogenic differentiation and that CCN2 operates downstream of this loss to promote chondrogenesis.


Subject(s)
Chondrogenesis/physiology , Focal Adhesion Kinase 1/metabolism , Immediate-Early Proteins/metabolism , Intercellular Signaling Peptides and Proteins/metabolism , Signal Transduction/physiology , src-Family Kinases/metabolism , Aggrecans/biosynthesis , Animals , Cell Differentiation/physiology , Cell Line, Transformed , Connective Tissue Growth Factor , DNA-Binding Proteins/biosynthesis , Extracellular Matrix/metabolism , Focal Adhesion Kinase 1/genetics , High Mobility Group Proteins/biosynthesis , Immediate-Early Proteins/genetics , Intercellular Signaling Peptides and Proteins/genetics , Mesoderm/cytology , Mesoderm/metabolism , Mice , SOXD Transcription Factors , Transcription Factors/biosynthesis , src-Family Kinases/genetics
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