Andrade Virginia, Echard Arnaud
CNRS UMR3691, Membrane Traffic and Cell Division Unit, Institut Pasteur, Université Paris Cité, Paris, France.
Collège Doctoral, Sorbonne Université, Paris, France.
Front Cell Dev Biol. 2022 Nov 24;10:1046617. doi: 10.3389/fcell.2022.1046617. eCollection 2022.
Cytokinetic abscission leads to the physical cut of the intercellular bridge (ICB) connecting the daughter cells and concludes cell division. In different animal cells, it is well established that the ESCRT-III machinery is responsible for the constriction and scission of the ICB. Here, we review the mechanical context of abscission. We first summarize the evidence that the ICB is initially under high tension and explain why, paradoxically, this can inhibit abscission in epithelial cells by impacting on ESCRT-III assembly. We next detail the different mechanisms that have been recently identified to release ICB tension and trigger abscission. Finally, we discuss whether traction-induced mechanical cell rupture could represent an ancient alternative mechanism of abscission and suggest future research avenues to further understand the role of mechanics in regulating abscission.
细胞分裂期的胞质分裂导致连接子细胞的细胞间桥(ICB)发生物理切断,从而结束细胞分裂。在不同的动物细胞中,已有充分证据表明内体分选转运复合体III(ESCRT-III)机制负责ICB的缢缩和切断。在此,我们综述胞质分裂的力学背景。我们首先总结ICB最初处于高张力状态的证据,并解释为何矛盾的是,这会通过影响ESCRT-III组装而抑制上皮细胞中的胞质分裂。接下来,我们详细阐述最近发现的释放ICB张力并触发胞质分裂的不同机制。最后,我们讨论牵引力诱导的机械性细胞破裂是否可能代表一种古老的胞质分裂替代机制,并提出未来的研究途径,以进一步了解力学在调节胞质分裂中的作用。