Polarized SCAR and the Arp2/3 complex regulate apical cortical remodeling in asymmetrically dividing neuroblasts

被引:1
作者
Cazzagon, Giulia [1 ]
Roubinet, Chantal [1 ]
Baum, Buzz [1 ]
机构
[1] Lab Mol Biol, Med Res Council, Cambridge CB2 0QH, England
基金
英国医学研究理事会;
关键词
CELL-SHAPE; ACTIN; CHROMOSOME; LOCALIZATION; CYTOKINESIS; ACTIVATION; MOVEMENT; PROTEINS; POSITION; DELTA;
D O I
10.1016/j.isci.2023.107129
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
Although the formin-nucleated actomyosin cortex has been shown to drive the changes in cell shape that accompany animal cell division in both symmetric and asymmetric cell divisions, the mitotic role of cortical Arp2/3-nucleated actin networks remain unclear. Here using asymmetrically dividing Drosophila neural stem cells as a model system, we identify a pool of membrane protrusions that form at the apical cortex of neuroblasts as they enter mitosis. Strikingly, these apically localized protrusions are enriched in SCAR, and depend on SCAR and Arp2/3 complexes for their formation. Because compromising SCAR or the Arp2/3 complex delays the apical clearance of Myosin II at the onset of anaphase and induces cortical instability at cytokinesis, these data point to a role for an apical branched actin filament network in fine-tuning the actomyosin cortex to enable the precise control of cell shape changes during an asymmetric cell division.
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页数:17
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