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Self-sorting of nonmuscle myosins IIA and IIB polarizes the cytoskeleton and modulates cell motility.非肌肉肌球蛋白IIA和IIB的自分选使细胞骨架极化并调节细胞运动。
J Cell Biol. 2017 Sep 4;216(9):2877-2889. doi: 10.1083/jcb.201705167. Epub 2017 Jul 12.
2
Adenomatous polyposis coli nucleates actin assembly to drive cell migration and microtubule-induced focal adhesion turnover.腺瘤性结肠息肉病蛋白促使肌动蛋白组装,以驱动细胞迁移和微管诱导的粘着斑周转。
J Cell Biol. 2017 Sep 4;216(9):2859-2875. doi: 10.1083/jcb.201702007. Epub 2017 Jun 29.
3
Long-range self-organization of cytoskeletal myosin II filament stacks.细胞骨架肌球蛋白 II 纤维束的远程自组织。
Nat Cell Biol. 2017 Feb;19(2):133-141. doi: 10.1038/ncb3466. Epub 2017 Jan 23.
4
Generation of contractile actomyosin bundles depends on mechanosensitive actin filament assembly and disassembly.收缩性肌动球蛋白束的产生取决于机械敏感的肌动蛋白丝组装和解聚。
Elife. 2015 Dec 10;4:e06126. doi: 10.7554/eLife.06126.
5
Talin determines the nanoscale architecture of focal adhesions.踝蛋白决定粘着斑的纳米级结构。
Proc Natl Acad Sci U S A. 2015 Sep 1;112(35):E4864-73. doi: 10.1073/pnas.1512025112. Epub 2015 Aug 17.
6
Structured illumination microscopy reveals focal adhesions are composed of linear subunits.结构照明显微镜显示粘着斑由线性亚基组成。
Cytoskeleton (Hoboken). 2015 May;72(5):235-45. doi: 10.1002/cm.21223.
7
The formin FMNL3 assembles plasma membrane protrusions that participate in cell-cell adhesion.formin FMNL3可组装参与细胞间黏附的质膜突起。
Mol Biol Cell. 2015 Feb 1;26(3):467-77. doi: 10.1091/mbc.E14-07-1247. Epub 2014 Nov 26.
8
Improved vectors and genome-wide libraries for CRISPR screening.用于CRISPR筛选的改良载体和全基因组文库。
Nat Methods. 2014 Aug;11(8):783-784. doi: 10.1038/nmeth.3047.
9
Stressing the limits of focal adhesion mechanosensitivity.强调粘着斑机械敏感性的局限性。
Curr Opin Cell Biol. 2014 Oct;30:68-73. doi: 10.1016/j.ceb.2014.06.003. Epub 2014 Jul 5.
10
A contractile and counterbalancing adhesion system controls the 3D shape of crawling cells.收缩和平衡的黏附系统控制着爬行细胞的 3D 形状。
J Cell Biol. 2014 Apr 14;205(1):83-96. doi: 10.1083/jcb.201311104. Epub 2014 Apr 7.

焦点黏附会纵向分裂成固定宽度的单位。

Focal Adhesions Undergo Longitudinal Splitting into Fixed-Width Units.

机构信息

Department of Biochemistry and Cell Biology, Geisel School of Medicine at Dartmouth, Hanover, NH 03755, USA.

Department of Biochemistry and Cell Biology, Geisel School of Medicine at Dartmouth, Hanover, NH 03755, USA.

出版信息

Curr Biol. 2018 Jul 9;28(13):2033-2045.e5. doi: 10.1016/j.cub.2018.04.073. Epub 2018 Jun 14.

DOI:10.1016/j.cub.2018.04.073
PMID:29910076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6061970/
Abstract

Focal adhesions (FAs) and stress fibers (SFs) act in concert during cell motility and in response to the extracellular environment. Although the structures of mature FAs and SFs are well studied, less is known about how they assemble and mature de novo during initial cell spreading. In this study using live-cell Airyscan microscopy, we find that FAs undergo "splitting" during their assembly, in which the FA divides along its longitudinal axis. Before splitting, FAs initially appear as assemblies of multiple linear units (FAUs) of 0.3-μm width. Splitting occurs between FAUs, resulting in mature FAs of either a single FAU or of a small number of FAUs that remain attached at their distal tips. Variations in splitting occur based on cell type and extracellular matrix. Depletion of adenomatous polyposis coli (APC) or vasodilator-stimulated phosphoprotein (VASP) results in reduced splitting. FA-associated tension increases progressively during splitting. Early in cell spreading, ventral SFs are detected first, with other SF sub-types (transverse arcs and dorsal SFs) being detected later. Our findings suggest that the fundamental unit of FAs is the fixed-width FAU, and that dynamic interactions between FAUs control adhesion morphology.

摘要

黏着斑(FAs)和应力纤维(SFs)在细胞运动和对外界环境的反应中协同作用。尽管成熟 FAs 和 SFs 的结构已经得到了很好的研究,但对于它们在初始细胞扩展过程中如何组装和成熟的了解较少。在这项使用活细胞 Airyscan 显微镜的研究中,我们发现 FAs 在其组装过程中会发生“分裂”,即在其纵轴上分裂。在分裂之前,FAs 最初表现为多个宽度为 0.3μm 的线性单位(FAUs)的组装。分裂发生在 FAUs 之间,导致成熟的 FAs 要么是一个 FAU,要么是少数几个在其远端尖端保持连接的 FAUs。根据细胞类型和细胞外基质的不同,分裂的情况也不同。腺瘤性结肠息肉病基因(APC)或血管扩张刺激磷蛋白(VASP)的耗竭会导致分裂减少。在分裂过程中,FA 相关的张力逐渐增加。在细胞扩展的早期,首先检测到腹侧 SFs,然后检测到其他 SF 亚型(横向弧形和背侧 SFs)。我们的发现表明,FAs 的基本单位是固定宽度的 FAU,并且 FAUs 之间的动态相互作用控制着黏附形态。