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通过实时成像和冷冻电子断层扫描揭示的细胞中肌动蛋白在对穿孔表面作出反应时的组织情况。

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

作者信息

Jasnin Marion, Ecke Mary, Baumeister Wolfgang, Gerisch Günther

机构信息

Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152 Martinsried, Germany.

Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152 Martinsried, Germany.

出版信息

Structure. 2016 Jul 6;24(7):1031-43. doi: 10.1016/j.str.2016.05.004. Epub 2016 Jun 16.

Abstract

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.

摘要

在三维环境中,运动细胞会根据几何线索来调节其伸出和缩回活动。在穿孔膜上迁移的盘基网柄菌细胞会围绕孔的边界形成肌动蛋白环,并通过自由空间延伸突起,以此来探索这些孔。当肌动蛋白波通过一个孔时,反应就会启动,并且这些环仅存在于被波包围的富含磷脂酰肌醇-3,4,5-三磷酸(PIP3)的区域。为了从冷冻电子断层扫描中重建肌动蛋白结构,通过冷冻相关光电子显微镜识别肌动蛋白环,并通过冷冻聚焦离子束铣削获得相关区域的薄楔形切片。通过肌球蛋白-II的积累来区分缩回阶段和伸出阶段。早期的肌动蛋白环由从膜上垂直伸出的细丝组成,这些细丝与靠近膜的细丝网络相互缠绕。后期识别出的分支表明,基于formin的细丝成核作用之后是Arp2/3介导的网络稳定作用,这防止了产生力的细丝发生屈曲。

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