Par Proteins and Neuronal Polarity

被引:29
|
作者
Insolera, Ryan [1 ,2 ]
Chen, She [1 ]
Shi, Song-Hai [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dev Biol Program, New York, NY 10065 USA
[2] Weill Cornell Med Coll, Grad Program Neurosci, New York, NY 10065 USA
关键词
neuronal polarity; PAR (for partitioning-defective) proteins; axon specification; cytoskeleton; signaling pathway; C-ELEGANS EMBRYOS; GLYCOGEN-SYNTHASE KINASE-3-BETA; DENDRITIC SPINE MORPHOGENESIS; ASYMMETRIC CELL DIVISIONS; UBIQUITIN LIGASE SMURF2; INTEGRIN-LINKED KINASE; AXON FORMATION; CAENORHABDITIS-ELEGANS; PHOSPHOINOSITIDE; 3-KINASE; CYTOPLASMIC LOCALIZATION;
D O I
10.1002/dneu.20867
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
A hallmark of neurons is their ability to polarize with dendrite and axon specification to allow the proper flow of information through the nervous system. Over the past decade, extensive research has been performed in an attempt to understand the molecular and cellular machinery mediating this neuronal polarization process. It has become evident that many of the critical regulators involved in establishing neuronal polarity are evolutionarily conserved proteins that had previously been implicated in controlling the polarization of other cell types. At the forefront of this research are the partition defective (Par) proteins. In this review, we will provide a commentary on the progress of work regarding the central importance of Par proteins in the establishment of neuronal polarity. (C) 2010 Wiley Periodicals, Inc. Develop Neurobiol 71: 483-494, 2011
引用
收藏
页码:483 / 494
页数:12
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