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非肌肉肌球蛋白 2A 和 2B 在间质细胞接触导向调节中的作用。

The role of nonmuscle myosin 2A and 2B in the regulation of mesenchymal cell contact guidance.

机构信息

Laboratory of Molecular Cardiology, National Heart, Lung, and Blood Institute, Bethesda, MD 20814.

Laboratory for Engineering in Oncology, University of Minnesota, Minneapolis, MN 55455.

出版信息

Mol Biol Cell. 2019 Jul 22;30(16):1961-1973. doi: 10.1091/mbc.E19-01-0071. Epub 2019 Jul 18.

Abstract

Contact guidance refers to the ability of cells to sense the geometrical features of the microenvironment and respond by changing their shape and adopting the appropriate orientation. Inhibition and ablation of nonmuscle myosin 2 (NM2) paralogues have demonstrated their importance for contact guidance. However, the specific roles of the NM2 paralogues have not been systematically studied. In this work we use micropatterned substrates to examine the roles of NM2A and NM2B and to elucidate the relationship of the microenvironment, actomyosin, and microtubules in contact guidance. We show that contact guidance is preserved following loss of NM2B and that expression of NM2A alone is sufficient to establish an appropriate orientation of the cells. Loss of NM2B and overexpression of NM2A result in a prominent cell polarization that is found to be linked to the increased alignment of microtubules with the actomyosin scaffold. Suppression of actomyosin with blebbistatin reduces cell polarity on a flat surface, but not on a surface with contact guidance cues. This indicates that the lost microtubule-actomyosin interactions are compensated for by microtubule-microenvironment interactions, which are sufficient to establish cell polarity through contact guidance.

摘要

接触导向是指细胞感知微环境的几何特征并通过改变形状和采用适当的方向来响应的能力。抑制和消融非肌肉肌球蛋白 2 (NM2) 同工酶已证明它们对接触导向很重要。然而,NM2 同工酶的具体作用尚未得到系统研究。在这项工作中,我们使用微图案化基底来研究 NM2A 和 NM2B 的作用,并阐明微环境、肌动球蛋白和微管在接触导向中的关系。我们表明,在 NM2B 缺失后,接触导向得以保留,并且单独表达 NM2A 足以建立细胞的适当取向。NM2B 的缺失和 NM2A 的过表达导致明显的细胞极化,这与微管与肌动球蛋白支架的对齐增加有关。用 blebbistatin 抑制肌动球蛋白会减少平面上的细胞极性,但不会减少具有接触导向线索的表面上的细胞极性。这表明失去的微管-肌动球蛋白相互作用被微管-微环境相互作用所补偿,这些相互作用足以通过接触导向建立细胞极性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/489d/6727766/5c7b94585d24/mbc-30-1961-g001.jpg

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