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由于黏附点和单个突起的局部对齐,肌球蛋白抑制作用下仍存在接触引导。

Contact guidance persists under myosin inhibition due to the local alignment of adhesions and individual protrusions.

机构信息

Department of Biology, James Madison University, Harrisonburg, VA, USA.

Department of Cell Biology, University of Virginia, Charlottesville, VA, USA.

出版信息

Sci Rep. 2017 Oct 30;7(1):14380. doi: 10.1038/s41598-017-14745-7.

Abstract

Contact guidance-cell polarization by anisotropic substrate features-is integral to numerous physiological processes; however the complexities of its regulation are only beginning to be discovered. In particular, cells polarize to anisotropic features under non-muscle myosin II (MII) inhibition, despite MII ordinarily being essential for polarized cell migration. Here, we investigate the ability of cells to sense and respond to fiber alignment in the absence of MII activity. We find that contact guidance is determined at the level of individual protrusions, which are individually guided by local fiber orientation, independent of MII. Protrusion stability and persistence are functions of adhesion lifetime, which depends on fiber orientation. Under MII inhibition, adhesion lifetime no longer depends on fiber orientation; however the ability of protrusions to form closely spaced adhesions sequentially without having to skip over gaps in adhesive area, biases protrusion formation along fibers. The co-alignment of multiple protrusions polarizes the entire cell; if the fibers are not aligned, contact guidance of individual protrusions still occurs, but does not produce overall cell polarization. These results describe how aligned features polarize a cell independently of MII and demonstrate how cellular contact guidance is built on the local alignment of adhesions and individual protrusions.

摘要

接触引导 - 细胞极化通过各向异性的基质特征 - 是许多生理过程的组成部分;然而,其调节的复杂性才刚刚开始被发现。特别是,尽管非肌肉肌球蛋白 II(MII)通常对于极化细胞迁移是必不可少的,但细胞仍在 MII 抑制下极化到各向异性特征。在这里,我们研究了细胞在没有 MII 活性的情况下感知和响应纤维排列的能力。我们发现接触引导是在单个突起的水平上确定的,这些突起分别由局部纤维取向引导,独立于 MII。突起的稳定性和持久性是粘附寿命的函数,而粘附寿命取决于纤维取向。在 MII 抑制下,粘附寿命不再取决于纤维取向;然而,突起形成紧密间隔的粘附物而无需跳过粘附区域中的间隙的能力,会沿着纤维偏向突起的形成。多个突起的共排列使整个细胞极化;如果纤维未对齐,单个突起的接触引导仍会发生,但不会产生整体细胞极化。这些结果描述了各向异性特征如何独立于 MII 来极化细胞,并展示了细胞接触引导如何建立在局部粘附和单个突起的对齐上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab4/5662575/896d9da15e1d/41598_2017_14745_Fig1_HTML.jpg

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