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Publication : Thrombospondin-1 signaling through CD47 inhibits cell cycle progression and induces senescence in endothelial cells.

First Author  Gao Q Year  2016
Journal  Cell Death Dis Volume  7
Issue  9 Pages  e2368
PubMed ID  27607583 Mgi Jnum  J:331038
Mgi Id  MGI:6871311 Doi  10.1038/cddis.2016.155
Citation  Gao Q, et al. (2016) Thrombospondin-1 signaling through CD47 inhibits cell cycle progression and induces senescence in endothelial cells. Cell Death Dis 7(9):e2368
abstractText  CD47 signaling in endothelial cells has been shown to suppress angiogenesis, but little is known about the link between CD47 and endothelial senescence. Herein, we demonstrate that the thrombospondin-1 (TSP1)-CD47 signaling pathway is a major mechanism for driving endothelial cell senescence. CD47 deficiency in endothelial cells significantly improved their angiogenic function and attenuated their replicative senescence. Lack of CD47 also suppresses activation of cell cycle inhibitors and upregulates the expression of cell cycle promoters, leading to increased cell cycle progression. Furthermore, TSP1 significantly accelerates replicative senescence and associated cell cycle arrest in a CD47-dependent manner. These findings demonstrate that TSP1-CD47 signaling is an important mechanism driving endothelial cell senescence. Thus, TSP1 and CD47 provide attractive molecular targets for treatment of aging-associated cardiovascular dysfunction and diseases involving endothelial dysregulation.
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