首页> 美国卫生研究院文献>Cell Regulation >Retrograde Flow and Myosin II Activity within the Leading Cell Edge Deliver F-Actin to the Lamella to Seed the Formation of Graded Polarity Actomyosin II Filament Bundles in Migrating Fibroblasts
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Retrograde Flow and Myosin II Activity within the Leading Cell Edge Deliver F-Actin to the Lamella to Seed the Formation of Graded Polarity Actomyosin II Filament Bundles in Migrating Fibroblasts

机译:细胞前缘内的逆行血流和肌球蛋白II活性将F-肌动蛋白传递给薄片以播种成纤维细胞中梯度极性的肌动球蛋白II丝束的形成。

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摘要

In migrating fibroblasts actomyosin II bundles are graded polarity (GP) bundles, a distinct organization to stress fibers. GP bundles are important for powering cell migration, yet have an unknown mechanism of formation. Electron microscopy and the fate of photobleached marks show actin filaments undergoing retrograde flow in filopodia, and the lamellipodium are structurally and dynamically linked with stationary GP bundles within the lamella. An individual filopodium initially protrudes, but then becomes separated from the tip of the lamellipodium and seeds the formation of a new GP bundle within the lamella. In individual live cells expressing both GFP-myosin II and RFP-actin, myosin II puncta localize to the base of an individual filopodium an average 28 s before the filopodium seeds the formation of a new GP bundle. Associated myosin II is stationary with respect to the substratum in new GP bundles. Inhibition of myosin II motor activity in live cells blocks appearance of new GP bundles in the lamella, without inhibition of cell protrusion in the same timescale. We conclude retrograde F-actin flow and myosin II activity within the leading cell edge delivers F-actin to the lamella to seed the formation of new GP bundles.
机译:在迁移的成纤维细胞中,放线菌素II束是分级极性(GP)束,是应力纤维的独特组织。 GP束对于促进细胞迁移很重要,但其形成机制却未知。电子显微镜和光漂白标记的命运表明肌动蛋白丝在丝状伪足中经历逆行流动,而lamellipodium与层状组织中的固定GP束在结构上和动态连接。一个单独的假单胞菌最初会突出,但随后会从片状脂质体的尖端分离出来,并在片状体内形成新的GP束。在表达GFP-肌球蛋白II和RFP-肌动蛋白的单个活细胞中,肌球蛋白II的斑点平均在单个假单胞菌的基部定位28 s,然后才形成新的GP束。关联的肌球蛋白II相对于新GP束中的基质是固定的。在活细胞中抑制肌球蛋白II运动活性可阻止新GP束在薄片中的出现,而不会在相同时间内抑制细胞的突出。我们得出结论,细胞前缘内的F-肌动蛋白逆行流动和肌球蛋白II活性将F-肌动蛋白传递至薄片,从而形成新的GP束。

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