血小板源性生长因子受体
下调和上调
血小板衍生生长因子
化学
缺氧(环境)
缺血
细胞生物学
磷酸酶
糖尿病
生长因子
医学
内分泌学
内科学
生物
癌症研究
磷酸化
受体
生物化学
氧气
有机化学
基因
作者
Clément Mercier,Tristan Brazeau,Jérémy Lamoureux,Elizabeth Boisvert,Stéphanie Robillard,Valérie Breton,Martin Paré,Andréanne Guay,Farah Lizotte,Marc‐Antoine Despatis,Pedro Geraldes
标识
DOI:10.1161/atvbaha.121.316638
摘要
Critical limb ischemia is a major complication of diabetes characterized by insufficient collateral vessel development and proper growth factor signaling unresponsiveness. Although mainly deactivated by hypoxia, phosphatases are important players in the deregulation of proangiogenetic pathways. Previously, SHP-1 (Scr homology 2-containing phosphatase-1) was found to be associated with the downregulation of growth factor actions in the diabetic muscle. Thus, we aimed to gain further understanding of the impact of SHP-1 on smooth muscle cell (SMC) function under hypoxic and diabetic conditions.
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