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通过E-cadherin稀释和actomyosin流动传递细胞动力
Diana Pinheiro1,2,3, Edouard Hannezo4,5, Sophie Herszterg1,2
1Institut Curie, PSL Research University, CNRS UMR 3215, INSERM U934, F-75248 Paris Cedex 05, France.
Nature
|March 16, 2017
概括
细胞分裂触发了邻近的上皮细胞中的机械信号,协调了细胞动力学过程中组织重塑的非肌肉肌肉素II (MyoII) 活动.
科学领域:
- 细胞生物学
- 发育生物学
- 生物物理
背景情况:
- 上皮细胞分裂需要重新塑造细胞与细胞的接触.
- 邻近细胞中的非肌肉肌肉素II (MyoII) 对于这一过程至关重要.
- 细胞分裂和MyoII活动之间的协调机制尚不清楚.
研究的目的:
- 调查协调上皮细胞运动和邻近细胞中的MyoII活动的机制.
- 阐明细胞分裂过程中的机械力量如何影响细胞-细胞粘附和actomyosin动态.
主要方法:
- 使用Drosophila notum表皮模型系统.
- 在细胞分裂过程中研究了机械感知和力传递事件.
- 分析了E-cadherin和非肌肉肌肉蛋白II (MyoII) 在附着结处的动态.
主要成果:
- 细胞分裂产生控制邻近细胞MyoII动态的机械信号.
- 环拉力会导致连接延长和E-cadherin稀释.
- 减少E-cadherin和细胞收缩性促进了actomyosin流动和MyoII积累.
结论:
- 一种新型的机械感知机制协调了表皮细胞在分裂过程中的动态.
- 这一过程在应对机械力时维持粘附接口的重塑.
- 突出了强力传导在细胞粘附动态中的替代作用.
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