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哺乳动物神经发育中的Par极性复合体

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  • 浙江工业大学生物与环境学院, 杭州 310014

收稿日期: 2012-08-27

  修回日期: 2012-11-15

  网络出版日期: 2013-03-25

基金资助

国家自然科学基金项目(编号:81241097)资助

Par polarity complex in mammalian neurogenesis

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  • College of Biological and Environment Engineering, Zhejiang University of Technology, Hangzhou 310014, China

Received date: 2012-08-27

  Revised date: 2012-11-15

  Online published: 2013-03-25

摘要

哺乳动物的神经发育过程极其复杂, 其形态结构和机能变化受到严格的调控。细胞极性是哺乳动物神经发生中最基本的特征之一, 在其调控因素中, Par极性复合体是研究最多的蛋白质。神经发育过程中Par蛋白的分布与量呈现动态变化, 影响细胞连接建立、细胞极性形成、神经突触发生及神经元迁移, 也影响到神经前体细胞的命运。文章主要从胚胎新皮层神经前体细胞及体外培养神经元角度, 总结了近年在Par极性蛋白的细胞内分布、机能及作用机制方面的研究进展。

本文引用格式

陈慧灵,陈晓萍 . 哺乳动物神经发育中的Par极性复合体[J]. 遗传, 2013 , 35(3) : 281 -286 . DOI: 10.3724/SP.J.1005.2013.00281

Abstract

Mammalian neurogenesis is a highly complicated process with programmed morphology and function evolution. Polarity, a basic characteristic in neurogenesis, is controlled by regulating proteins such as the partition defective (Par) proteins. Par polarity complex is the most investigated Par protein among these polarity proteins. There are developmental dynamic changes during neurogenesis for the protein distribution and content, which are related to the junction establishment, polarity formation, synaptogenesis, and neuronal migration. Moreover, Par complex is considered to affect the devel-opmental fate of neural precursors. This study summarizes the advances of the protein cellular location, function, and mechanism in embryal neocortex and cultured neuron.

参考文献

[1] Kemphues KJ, Priess JR, Morton DG, Cheng NS. Identification of genes required for cytoplasmic localization in early C. elegans embryos. Cell, 1988, 52(3): 311-320.
[2] Namba T, Nakamuta S, Funahashi Y, Kaibuchi K. The role of selective transport in neuronal polarization. Dev Neurobiol, 2011, 71(6): 445-457.
[3] Arimura N, Kaibuchi K. Neuronal polarity: from ex-tracellular signals to intracellular mechanisms. Nat Rev Neurosci, 2007, 8(3): 194-205.
[4] Watanabe T, Noritake J, Kaibuchi K. Regulation of microtubules in cell migration. Trends Cell Biol, 2005, 15(2): 76-83.
[5] Levitan DJ, Boyd L, Mello CC, Kemphues KJ, Stinch-comb DT. Par-2, a gene required for blastomere asymmetry in Caenorhabditis elegans, encodes zinc-finger and ATP-binding motifs. Proc Natl Acad Sci USA, 1994, 91(13): 6108-6112.
[6] Etemad-Moghadam B, Guo S, Kemphues KJ. Asymmetri-cally distributed PAR-3 protein contributes to cell polarity and spindle alignment in early C. elegans embryos. Cell, 1995, 83(5): 743-752.
[7] Guo S, Kemphues KJ. Par-1, a gene required for estab-lishing polarity in C. elegans embryos, encodes a putative Ser/Thr kinase that is asymmetrically distributed. Cell, 1995, 81(4): 611-620.
[8] Hung TJ, Kemphues KJ. PAR-6 is a conserved PDZ do-main-containing protein that colocalizes with PAR-3 in Caenorhabditis elegans embryos. Development, 1999, 126(1): 127-135.
[9] Watts JL, Morton DG, Bestman J, Kemphues KJ. The C. elegans par-4 gene encodes a putative serine-threonine kinase required for establishing embryonic asymmetry. Development, 2000, 127(7): 1467-1475.
[10] Morton DG, Shakes DC, Nugent S, Dichoso D, Wang WF, Golden A, Kemphues KJ. The Caenorhabditis elegans par-5 gene encodes a 14-3-3 protein required for cellular asymmetry in the early embryo. Dev Biol, 2002, 241(1): 47-58.
[11] Böhm H, Brinkmann V, Drab M, Henske A, Kurzchalia TV. Mammalian homologues of C. elegans PAR-1 are asym-metrically localized in epithelial cells and may influence their polarity. Curr Biol, 1997, 7(8): 603-606.
[12] Zhou Y. Cortical development and asymmetric cell divi-sions. Front Biol, 2012, 7(4): 297-306.
[13] Lin D, Edwards AS, Fawcett JP, Mbamalu G, Scott JD, Pawson T. A mammalian PAR-3-PAR-6 complex implicated in Cdc42/Rac1 and aPKC signalling and cell polarity. Nat Cell Biol, 2000, 2(8): 540-547.
[14] Watts JL, Etemad-Moghadam B, Guo S, Boyd L, Draper BW, Mello CC, Priess JR, Kemphues KJ. Par-6, a gene involved in the establishment of asymmetry in early C. elegans embryos, mediates the asymmetric localization of PAR-3. Development, 1996, 122(10): 3133-3140.
[15] Suzuki A, Akimoto K, Ohno S. Protein kinase C λ/ι (PKC λ/ι): a PKC isotype essential for the development of mul-ticellular organisms. J Biochem, 2003, 133(1): 9-16.
[16] Komada M, Soriano P. Hrs, a FYVE finger protein local-ized to early endosomes, is implicated in vesicular traffic and required for ventral folding morphogenesis. Genes Dev, 1999, 13(11): 1475-1485.
[17] Farkas LM, Huttner WB. The cell biology of neural stem and progenitor cells and its significance for their prolif-eration versus differentiation during mammalian brain development. Curr Opin Cell Biol, 2008, 20(6): 707-715.
[18] Nadarajah B, Alifragis P, Wong ROL, Parnavelas JG. Neuronal migration in the developing cerebral cortex: ob-servations based on real-time imaging. Cereb Cor-tex, 2003, 13(6): 607-611.
[19] Smart IHM. Three dimensional growth of the mouse iso-cortex. J Anat, 1983, 137(4): 683-694.
[20] Noctor SC, Flint AC, Weissman TA, Dammerman RS, Kriegstein AR. Neurons derived from radial glial cells es-tablish radial units in neocortex. Nature, 2001, 409(6821): 714-720.
[21] Noctor SC, Martínez-Cerdeño V, Kriegste
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