Cell size and polarization determine cytokinesis furrow ingression dynamics in mouse embryos

被引:8
|
作者
Paim, Lia Mara Gomes [1 ]
FitzHarris, Greg [1 ,2 ,3 ]
机构
[1] Ctr Hosp Univ Montreal, Ctr Rech, Montreal, PQ H2X 0A9, Canada
[2] Univ Montreal, Dept Obstet Gynecol, Montreal, PQ H3C 3J7, Canada
[3] Univ Montreal, Dept Pathol & Biol Cellulaire, Montreal, PQ H3T 1J4, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
cytokinesis; cell polarity; embryo development; contractile ring; furrow ingression; CHROMOSOME SEGREGATION; CONTRACTILE RING; ACTOMYOSIN RING; ANGIOMOTIN; PROTEINS; DIVISION; POSITION; SHIFT; FATE; AXIS;
D O I
10.1073/pnas.2119381119
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cytokinesis is the final step of cell division during which a contractile ring forms a furrow that partitions the cytoplasm in two. How furrow ingression is spatiotemporally regulated and how it is adapted to complex cellular environments and developmental transitions remain poorly understood. Here, we examine furrow ingression dynamics in the context of the early mouse embryo and find that cell size is a powerful determinant of furrow ingression speed during reductive cell divisions. In addition, the emergence of cell polarity and the assembly of the apical domain in outer cells locally inhibits the recruitment of cytokinesis components and thereby negatively regulates furrow ingression specifically on one side of the furrow. We show that this biasing of cytokinesis is not dependent upon cell-cell adhesion or shape but rather is cell intrinsic and is caused by a paucity of cytokinetic machinery in the apical domain The results thus reveal that in the mouse embryo cell polarity directly regulates the recruitment of cytokinetic machinery in a cell-autonomous manner and that subcellular organization can instigate differential force generation and constriction speed in different zones of the cytokinetic furrow.
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页数:10
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