皮层张力中的异位变异揭示了极化皮层流动的物理基础
Mirjam Mayer1, Martin Depken, Justin S Bois
1Max Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.
Nature
|September 21, 2010
概括
在Caenorhabditis elegans zygotes中,大规模的皮层流对于细胞两极分化至关重要. 这项研究表明,皮质张力中的异质,而不是张力梯度,驱动了这种流动,需要actomyosin收缩度梯度和足够的皮质粘度.
科学领域:
- 细胞生物学 细胞生物学
- 发育生物学 发展生物学
- 生物物理学的生物物理.
背景情况:
- 不对称的细胞分裂对于多细胞生物的发展至关重要.
- 对称细胞的两极分化,就像Caenorhabditis elegans zygote一样,在不对称分裂之前发生.
- 阿克托米奥辛皮层的大规模流动是C. elegans zygote的前后两极分化的关键,但其物理驱动因素尚不清楚.
研究的目的:
- 为了研究在极化C. elegans zygotes中皮层张力的亚细胞分布.
- 阐明控制大规模actomyosin皮质流动的物理原理和力量.
- 了解在产生细胞不对称性时,actomyosin收缩性和皮质张力之间的相互作用.
主要方法:
- 利用位置和方向敏感的激光切除来测量亚细胞皮质张力.
- 结合实验数据与主动皮层力学理论建模.
- 分析了皮层张力分布和皮层流动力学之间的关系.
主要成果:
- 皮质流是由皮质张力中的异构 (不同方向的属性差异) 驱动的,而不是梯度 (跨空间的属性差异).
- 证明,为了启动皮层流动,需要对actomyosin收缩性的梯度.
- 确定了足够的皮质粘度作为长距离皮质流动的先决条件.
结论:
- 大规模的皮质流需要收缩梯度来驱动运动和高粘度来实现远程传播.
- 这些发现挑战了先前的假设,认为张力梯度是皮层流动的主要驱动因素.
- 这项研究澄清了细胞内皮层流的物理要求,这对于C. elegans的胚胎偏向至关重要.
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