首页> 外文期刊>Journal of cell biology >CYRI-A limits invasive migration through macropinosome formation and integrin uptake regulation
【24h】

CYRI-A limits invasive migration through macropinosome formation and integrin uptake regulation

机译:Cyri-A通过Macroposome形成和整合素的摄取调节限制侵袭性迁移

获取原文
           

摘要

The Scar/WAVE complex drives actin nucleation during cell migration. Interestingly, the same complex is important in forming membrane ruffles during macropinocytosis, a process mediating nutrient uptake and membrane receptor trafficking. Mammalian CYRI-B is a recently described negative regulator of the Scar/WAVE complex by RAC1 sequestration, but its other paralogue, CYRI-A, has not been characterized. Here, we implicate CYRI-A as a key regulator of macropinosome formation and integrin internalization. We find that CYRI-A is transiently recruited to nascent macropinosomes, dependent on PI3K and RAC1 activity. CYRI-A recruitment precedes RAB5A recruitment but follows sharply after RAC1 and actin signaling, consistent with it being a local inhibitor of actin polymerization. Depletion of both CYRI-A and -B results in enhanced surface expression of the α5β1 integrin via reduced internalization. CYRI depletion enhanced migration, invasion, and anchorage-independent growth in 3D. Thus, CYRI-A is a dynamic regulator of macropinocytosis, functioning together with CYRI-B to regulate integrin trafficking.
机译:瘢痕/波复合物在细胞迁移期间驱动肌动蛋白成核。有趣的是,相同的复合物在癌细胞增生期间在形成膜荷叶边的过程中是重要的,该方法介导营养吸收和膜受体贩运。哺乳动物Cyri-B是最近描述的疤痕/波复合物的负调节器通过RAC1封存,但其其他普拉拉因犬Cyri-A尚未表征。在这里,我们将Cyri-A致癌为Macroposome形成和整合素内化的关键调节剂。我们发现Cyri-A瞬间募集到依赖于PI3K和RAC1活性的新生宏观体瘤。 Cyri-A募集在RAB5A募集后,但在RAC1和肌动蛋白信号传导后急剧下列,与其成为肌动蛋白聚合的局部抑制剂。 Cyri-A和-B的耗竭导致通过降低的内化提高α5β1整联蛋白的表面表达。 Cyri耗尽增强了3D的迁移,入侵和锚定无关。因此,Cyri-A是Macropoinocytosis的动态调节剂,与Cyri-B一起运作,以调节整联曲行贩运。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号