首页> 美国卫生研究院文献>PLoS Clinical Trials >Comparative Dynamics of Retrograde Actin Flow and Focal Adhesions: Formation of Nascent Adhesions Triggers Transition from Fast to Slow Flow
【2h】

Comparative Dynamics of Retrograde Actin Flow and Focal Adhesions: Formation of Nascent Adhesions Triggers Transition from Fast to Slow Flow

机译:逆行肌动蛋白血流和局灶性黏附的比较动力学:新生黏附的形成触发从快速流动到缓慢流动的转变

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Dynamic actin network at the leading edge of the cell is linked to the extracellular matrix through focal adhesions (FAs), and at the same time it undergoes retrograde flow with different dynamics in two distinct zones: the lamellipodium (peripheral zone of fast flow), and the lamellum (zone of slow flow located between the lamellipodium and the cell body). Cell migration involves expansion of both the lamellipodium and the lamellum, as well as formation of new FAs, but it is largely unknown how the position of the boundary between the two flow zones is defined, and how FAs and actin flow mutually influence each other. We investigated dynamic relationship between focal adhesions and the boundary between the two flow zones in spreading cells. Nascent FAs first appeared in the lamellipodium. Within seconds after the formation of new FAs, the rate of actin flow decreased locally, and the lamellipodium/lamellum boundary advanced towards the new FAs. Blocking fast actin flow with cytochalasin D resulted in rapid dissolution of nascent FAs. In the absence of FAs (spreading on poly-L-lysine-coated surfaces) retrograde flow was uniform and the velocity transition was not observed. We conclude that formation of FAs depends on actin dynamics, and in its turn, affects the dynamics of actin flow by triggering transition from fast to slow flow. Extension of the cell edge thus proceeds through a cycle of lamellipodium protrusion, formation of new FAs, advance of the lamellum, and protrusion of the lamellipodium from the new base.
机译:细胞前缘的动态肌动蛋白网络通过粘着斑(FA)与细胞外基质相连,同时又在两个不同的区域经历具有不同动力学的逆行流动:lamellipodium(快速流动的外围区域),薄层(慢流区域位于薄层脂质体和细胞体之间)。细胞迁移涉及lamellipodium和lamilum的膨胀,以及新FA的形成,但在很大程度上未知如何定义两个流动区之间的边界位置以及FA和肌动蛋白流如何相互影响。我们研究了粘着斑与扩散细胞中两个流动区域之间的边界之间的动态关系。新生的FAs首先出现在片状脂质体中。在新的FA形成后的几秒钟内,肌动蛋白的流速局部降低,并且lamellipodium / lamellum边界向新的FA推进。用细胞松弛素D阻止肌动蛋白的快速流动导致新生FA的快速溶解。在不存在FA的情况下(在聚L-赖氨酸涂层表面扩散),逆流是均匀的,没有观察到速度变化。我们得出结论,FA的形成取决于肌动蛋白的动力学,进而通过触发从快流到慢流的转变来影响肌动蛋白流的动力学。因此,细胞边缘的延伸通过lamellipodium突出,新FA的形成,lamilum的前进以及lamellipodium从新碱基突出的循环来进行。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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