PAR3-PAR6-atypical PKC polarity complex proteins in neuronal polarization

被引:29
|
作者
Hapak, Sophie M. [1 ]
Rothlin, Carla V. [2 ,4 ]
Ghosh, Sourav [3 ,4 ]
机构
[1] Univ Minnesota, Sch Med, Dept Med, 401 East River Pkwy, Minneapolis, MN 55455 USA
[2] Yale Univ, Sch Med, Dept Immunobiol, 300 Cedar St, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Neurol, 300 George St, New Haven, CT 06511 USA
[4] Yale Univ, Sch Med, Dept Pharmacol, 333 Cedar St, New Haven, CT 06520 USA
关键词
PKM zeta; Axon specification; Dendritogenesis; Signaling; Wnt; Crumbs; CDC42/RAC; GLYCOGEN-SYNTHASE KINASE-3-BETA; KINASE-C-ZETA; TUMOR-SUPPRESSOR GENE; EPITHELIAL-CELL POLARITY; ADHESION MOLECULE TAG-1; RETINAL GANGLION-CELLS; LIPID PHOSPHATASE PTEN; GTP-BINDING-PROTEIN; INDUCED AXON GROWTH; N-TERMINAL KINASE;
D O I
10.1007/s00018-018-2828-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polarity is a fundamental feature of cells. Protein complexes, including the PAR3-PAR6-aPKC complex, have conserved roles in establishing polarity across a number of eukaryotic cell types. In neurons, polarity is evident as distinct axonal versus dendritic domains. The PAR3, PAR6, and aPKC proteins also play important roles in neuronal polarization. During this process, either aPKC kinase activity, the assembly of the PAR3-PAR6-aPKC complex or the localization of these proteins is regulated downstream of a number of signaling pathways. In turn, the PAR3, PAR6, and aPKC proteins control various effector molecules to establish neuronal polarity. Herein, we discuss the many signaling mechanisms and effector functions that have been linked to PAR3, PAR6, and aPKC during the establishment of neuronal polarity.
引用
收藏
页码:2735 / 2761
页数:27
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