ACS Synth Biol. 2020 Apr 17;9(4):902-919. doi: 10.1021/acssynbio.9b00521. Epub 2020 Mar 16.
Cleavage furrow formation during cytokinesis involves extensive membrane remodeling. In the absence of methods to exert dynamic control over these processes, it has been a challenge to examine the basis of this remodeling. Here we used a subcellular optogenetic approach to induce this at will and found that furrow formation is mediated by actomyosin contractility, retrograde plasma membrane flow, localized decrease in membrane tension, and endocytosis. FRAP, 4-D imaging, and inhibition or upregulation of endocytosis or exocytosis show that ARF6 and Exo70 dependent localized exocytosis supports a potential model for intercellular bridge elongation. TIRF and Super Resolution Radial Fluctuation (SRRF) stream microscopy show localized VAMP2-mediated exocytosis and incorporation of membrane lipids from vesicles into the plasma membrane at the front edge of the nascent daughter cell. Thus, spatially separated but coordinated plasma membrane depletion and addition are likely contributors to membrane remodeling during cytokinetic processes.
有丝分裂过程中的分裂沟形成涉及广泛的膜重塑。由于缺乏对这些过程进行动态控制的方法,因此研究这种重塑的基础一直是一个挑战。在这里,我们使用亚细胞光遗传学方法来随意诱导这种过程,发现沟的形成是由肌动球蛋白收缩性、逆行质膜流动、局部膜张力降低和胞吞作用介导的。FRAP、4-D 成像以及胞吞作用或胞吐作用的抑制或上调表明,ARF6 和 Exo70 依赖性的局部胞吐作用支持细胞间桥伸长的潜在模型。TIRF 和超分辨率径向波动(SRRF)流显微镜显示,局部 VAMP2 介导的胞吐作用以及从囊泡中将膜脂质掺入到新生子细胞的质膜前缘。因此,在有丝分裂过程中,空间上分离但协调的质膜耗竭和添加可能是膜重塑的贡献因素。