Myosin cluster dynamics determines epithelial wound ring constriction

Alka Bhat, Remi Berthoz, Simon Lo Vecchio, Coralie Spiegelhalter, Shigenobu Yonemura, Olivier Pertz, Daniel Riveline
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Abstract

Collection of myosin motors and actin filaments can self-assemble into submicrometric clusters under the regulation of RhoA. Emergent dynamics of these clusters have been reported in a variety of morphogenetic systems, ranging from Drosophila to acto-myosin assays in vitro. In single cell cytokinetic rings, acto-myosin clusters are associated with stress generation when radial and transport when tangential with respect to the ring closure. Here, we show that these phenomena hold true for acto-myosin multi-cellular rings during wound closure in epithelial monolayers. We assessed the activity of RhoA using FRET sensors, and we report that cluster dynamics does not correlate with RhoA activity. Nevertheless, we show that bursts of RhoA activation precede recruitment of myosin. Altogether myosin clusters dynamics is conserved between single and multi-cellular systems and this suggests that they could be used as generic read-outs for mapping and predicting stress generation and shape changes in morphogenesis.
肌球蛋白簇动力学决定上皮伤口环收缩
在 RhoA 的调控下,肌球蛋白马达和肌动蛋白丝的集合可以自组装成亚微米级的簇。从果蝇到体外肌动蛋白试验等各种形态发生系统都报道了这些集群的新动态。在单细胞细胞运动环中,肌动蛋白簇与环闭合时的径向应力产生和切向应力运输有关。在这里,我们发现在上皮单层细胞伤口闭合过程中,肌动蛋白多细胞环也存在这些现象。我们使用 FRET 传感器对 RhoA 的活性进行了评估,结果发现簇的动态与 RhoA 的活性并不相关。然而,我们发现在肌球蛋白招募之前会出现 RhoA 激活爆发。总之,肌球蛋白簇的动态在单细胞和多细胞系统之间是一致的,这表明它们可以用作绘制和预测形态发生过程中应力产生和形状变化的通用读出器。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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