| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2176942 | Developmental Cell | 2013 | 15 Pages |
•MT1-MMP directs osteogenic, chondrogenic, and adipogenic fate decisions•MT1-MMP controls stem cell commitment by remodeling the 3D extracellular matrix•MT1-MMP-dependent control of 3D cell-shape changes activates β1-integrin signaling•MT1-MMP controls lineage commitment by triggering a β1-integrin/YAP/TAZ network
SummaryIn vitro, topographical and biophysical cues arising from the extracellular matrix (ECM) direct skeletal stem cell (SSC) commitment and differentiation. However, the mechanisms by which the SSC-ECM interface is regulated and the outcome of such interactions on stem cell fate in vivo remain unknown. Here we demonstrate that conditional deletion of the membrane-anchored metalloproteinase MT1-MMP (Mmp14) in mesenchymal progenitors, but not in committed osteoblasts, redirects SSC fate decisions from osteogenesis to adipo- and chondrogenesis. By effecting ECM remodeling, MT1-MMP regulates stem cell shape, thereby activating a β1-integrin/RhoGTPase signaling cascade and triggering the nuclear localization of the transcriptional coactivators YAP and TAZ, which serve to control SSC lineage commitment. These data identify a critical MT1-MMP/integrin/YAP/TAZ axis operative in the stem cell niche that oversees SSC fate determination.
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