首页> 外文OA文献 >Actin Organization in Cells Responding to a Perforated Surface, Revealed by Live Imaging and Cryo-Electron Tomography
【2h】

Actin Organization in Cells Responding to a Perforated Surface, Revealed by Live Imaging and Cryo-Electron Tomography

机译:细胞中的肌动蛋白组织响应穿孔表面,通过实时成像和低温电子断层扫描显示

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

In a 3D environment, motile cells accommodate their protruding and retracting activities to geometrical cues. Dictyostelium cells migrating on a perforated film explored its holes by forming actin rings around their border and extending protrusions through the free space. The response was initiated when an actin wave passed a hole, and the rings persisted only in the PIP3-rich territories surrounded by a wave. To reconstruct actin structures from cryo-electron tomograms, actin rings were identified by cryo-correlative light and electron microscopy, and thin wedges of relevant regions were obtained by cryo-focused ion-beam milling. Retracting stages were distinguished from protruding ones by the accumulation of myosin-II. Early actin rings consisted of filaments pointing upright from the membrane, entangled with a meshwork of filaments close to the membrane. Branches identified at later stages suggested that formin-based nucleation of filaments was followed by Arp2/3-mediated network stabilization, which prevented buckling of the force-generating filaments.
机译:在3D环境中,活动单元适应其几何提示的突出和缩回活动。迁移到穿孔膜上的Dictyostelium细胞通过在其边界周围形成肌动蛋白环并延伸穿过自由空间的突起来探索其孔。当肌动蛋白波通过一个孔时,反应开始,并且环仅在被波包围的富含PIP3的区域中持续存在。为了从低温电子断层图重建肌动蛋白结构,通过低温相关光和电子显微镜鉴定肌动蛋白环,并通过低温聚焦离子束研磨获得相关区域的细楔形。收缩期与突出期的区别在于肌球蛋白II的积累。早期的肌动蛋白环由从膜上直立的细丝组成,缠绕在靠近膜的细丝网状结构上。在较晚阶段发现的分支表明,基于长效蛋白的长丝成核之后是Arp2 / 3介导的网络稳定作用,这可以防止力产生丝的屈曲。

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