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首页> 外文期刊>Cell adhesion & migration >MAGI1 localizes to mature focal adhesion and modulates endothelial cell adhesion, migration and angiogenesis
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MAGI1 localizes to mature focal adhesion and modulates endothelial cell adhesion, migration and angiogenesis

机译:MAGI1定位于成熟局灶性粘附性,并调节内皮细胞粘附,迁移和血管生成

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MAGI1 is an intracellular adaptor protein that stabilizes cell junctions and regulates epithelial and endothelial integrity. Here, we report that that in endothelial cells MAGI1 colocalizes with paxillin, β3-integrin, talin 1, tensin 3 and α-4-actinin at mature focal adhesions and actin stress fibers, and regulates their dynamics. Downregulation of MAGI1 reduces focal adhesion formation and maturation, cell spreading, actin stress fiber formation and RhoA/Rac1 activation. MAGI1 silencing increases phosphorylation of paxillin at Y118, an indicator of focal adhesion turnover. MAGI1 promotes integrin-dependent?endothelial cells adhesion to ECM, reduces invasion and tubulogenesis in?vitro and suppresses?angiogenesis in?vivo . Our results identify MAGI1 as anovel component of focal adhesions, and regulator of focal adhesion dynamics, cell adhesion, invasion and angiogenesis.
机译:MAGI1是一种细胞内适配器蛋白,其稳定细胞连接并调节上皮和内皮完整性。 在这里,我们认为,在内皮细胞中,Magi1在成熟局部粘连和肌动蛋白应力纤维上用帕毛蛋白,β3-整联蛋白,瞳孔1,β3-整合蛋白,瞳孔1,β3-1-14-14-猕猴蛋白结合,并调节其动力学。 MAGI1的下调减少了局灶性粘附形成和成熟,细胞扩散,肌动蛋白应激纤维形成和RHOA / RAC1活化。 MAGI1沉默增加了Y118在Y118,局灶性粘附转换的指标增加了paxillin的磷酸化。 MAGI1促进整合素相关的?内皮细胞对ECM的粘附性,减少了体外侵袭和小管生成并抑制?体内血管生成。 我们的结果鉴定MAGI1作为局灶性粘连的Anovel组分,以及局灶性粘附动力学,细胞粘附,侵袭和血管生成的调节器。

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