| First Author | Chen SZ | Year | 2016 |
| Journal | Cell Death Differ | Volume | 23 |
| Issue | 11 | Pages | 1778-1791 |
| PubMed ID | 27447109 | Mgi Jnum | J:258525 |
| Mgi Id | MGI:6140570 | Doi | 10.1038/cdd.2016.66 |
| Citation | Chen SZ, et al. (2016) The miR-181d-regulated metalloproteinase Adamts1 enzymatically impairs adipogenesis via ECM remodeling. Cell Death Differ 23(11):1778-1791 |
| abstractText | The extracellular matrix (ECM) maintenance is crucial to the structural integrity of adipocytes and whole adipose tissue formation. However, the potential impact of the ECM on adipocyte lineage commitment is unclear. Herein, we demonstrate that forced expression of matrix-associated metalloproteinase Adamts1 (a disintegrin and metalloproteinase with thrombospondin motifs 1), which we show is targeted by microRNA-181d (miR-181d) during BMP4-induced adipocytic lineage commitment, markedly impairs adipocyte commitment. Conversely, siRNA-induced inhibition of Adamts1 promotes adipocyte commitment. Adamst1 metalloprotease activity is required for this inhibition and is determined to function via remodeling ECM components followed by activating FAK-ERK signaling pathway during the commitment process. Furthermore, ablation of Adamts1 in adipose tissue increases adipose tissue mass, reduces insulin sensitivity, and disrupts lipid homeostasis. This finding is consistent with Adamts1 decreased expression in the adipose tissue of obese mice and an inverse correlation of Adamts1 expression with body mass index in humans. Collectively, our results indicate that Adamts1 acts as an ECM ''modifier'', with miR-181d-induced downregulation, that regulates adipocyte lineage commitment and obesity. |
