DAPLE orchestrates apical actomyosin assembly from junctional polarity complexes.
DAPLE orchestrates apical actomyosin assembly from junctional polarity complexes.
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DOI:
10.1083/jcb.202111002
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发表时间:
2022-05-02
期刊:
影响因子:
--
通讯作者:
Garcia-Marcos M
中科院分区:
文献类型:
--
作者:
Marivin A;Ho RX;Garcia-Marcos M
Marivin et al. show how association of the protein DAPLE with PAR polarity complexes at cell–cell junctions maintains an apical cytoskeletal network in epithelial cells by simultaneously activating heterotrimeric G proteins and recruiting the actin-stabilizing protein CD2AP. Establishment of apicobasal polarity and the organization of the cytoskeleton must operate coordinately to ensure proper epithelial cell shape and function. However, the precise molecular mechanisms by which polarity complexes directly instruct the cytoskeletal machinery to determine cell shape are poorly understood. Here, we define a mechanism by which the PAR polarity complex (PAR3–PAR6–aPKC) at apical cell junctions leads to efficient assembly of the apical actomyosin network to maintain epithelial cell morphology. We found that the PAR polarity complex recruits the protein DAPLE to apical cell junctions, which in turn triggers a two-pronged mechanism that converges upon assembly of apical actomyosin. More specifically, DAPLE directly recruits the actin-stabilizing protein CD2AP to apical junctions and, concomitantly, activates heterotrimeric G protein signaling in a GPCR-independent manner to favor RhoA-myosin activation. These observations establish DAPLE as a direct molecular link between junctional polarity complexes and the formation of apical cytoskeletal assemblies that support epithelial cell shape.
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