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核和核-细胞骨架连接在三维细胞迁移中的独特作用。

The distinct roles of the nucleus and nucleus-cytoskeleton connections in three-dimensional cell migration.

机构信息

Department of Chemical and Biomolecular Engineering, The Johns Hopkins University, Baltimore, Maryland 21218, USA.

出版信息

Sci Rep. 2012;2:488. doi: 10.1038/srep00488. Epub 2012 Jul 3.

Abstract

Cells often migrate in vivo in an extracellular matrix that is intrinsically three-dimensional (3D) and the role of actin filament architecture in 3D cell migration is less well understood. Here we show that, while recently identified linkers of nucleoskeleton to cytoskeleton (LINC) complexes play a minimal role in conventional 2D migration, they play a critical role in regulating the organization of a subset of actin filament bundles - the perinuclear actin cap - connected to the nucleus through Nesprin2giant and Nesprin3 in cells in 3D collagen I matrix. Actin cap fibers prolong the nucleus and mediate the formation of pseudopodial protrusions, which drive matrix traction and 3D cell migration. Disruption of LINC complexes disorganizes the actin cap, which impairs 3D cell migration. A simple mechanical model explains why LINC complexes and the perinuclear actin cap are essential in 3D migration by providing mechanical support to the formation of pseudopodial protrusions.

摘要

细胞在体内经常在固有三维(3D)的细胞外基质中迁移,而肌动蛋白丝结构在 3D 细胞迁移中的作用还不太清楚。在这里,我们发现,尽管最近鉴定的核骨架-细胞骨架(LINC)复合物连接物在传统的 2D 迁移中作用很小,但它们在调节一组肌动蛋白丝束的组织中起着关键作用-核周肌动蛋白帽-通过 Nesprin2giant 和 Nesprin3 在 3D 胶原 I 基质中的细胞与核相连。肌动蛋白帽纤维延长了细胞核,并介导了伪足突起的形成,从而驱动基质牵引力和 3D 细胞迁移。LINC 复合物的破坏会使肌动蛋白帽紊乱,从而阻碍 3D 细胞迁移。一个简单的力学模型解释了为什么 LINC 复合物和核周肌动蛋白帽在 3D 迁移中是必不可少的,因为它为伪足突起的形成提供了机械支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdf5/3388469/dc589f3c2b55/srep00488-f1.jpg

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