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G蛋白偶联受体在血管发育中的作用

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  • 上海交通大学医学院, 中国科学院上海生命科学研究院健康科学研究所干细胞生物学重点实验室, 上海 200025

收稿日期: 2012-05-08

  修回日期: 2012-08-24

  网络出版日期: 2013-04-25

基金资助

国家自然科学基金重点项目(编号:81130005)资助

G protein-coupled receptors in vascular development

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  • Key Laboratory of Stem Cell Biology, Institute of Health Sciences, Shanghai Jiao Tong University School of Medicine & Shanghai Insti-tutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200025, China

Received date: 2012-05-08

  Revised date: 2012-08-24

  Online published: 2013-04-25

摘要

血管发育包括血管发生和血管生成两个阶段。近年研究表明, G蛋白偶联受体广泛参与调控成血管细胞的分化、迁移和接合, 尖端细胞和柄细胞命运决定, 内皮细胞的增殖、迁移和管腔形成等多个过程。文章以血管发育中的这些关键事件为主线, 总结了G蛋白偶联受体家族成员特别是视紫红质类和卷曲类受体在调节血管发育方面的最新研究进展。文章着重介绍了斑马鱼作为模式生物在血管发育生物学研究中的独特优势, 并展望了利用斑马鱼深入开展G蛋白偶联受体相关研究的广阔前景。

本文引用格式

李方方 李文庆 荆清 . G蛋白偶联受体在血管发育中的作用[J]. 遗传, 2013 , 35(4) : 459 -467 . DOI: 10.3724/SP.J.1005.2013.00459

Abstract

The vascular development consists of two continuous processes: vasculogenesis and angiogenesis. Some researches showed that G protein-coupled receptors (GPCRs) play important roles in these processes, including the regulation of differentiation, migration and coalescence of angioblasts, fate decision of tip and stalk cells, proliferation and migration of endothelial cells and tube formation. For the key events of vasculogenesis and angiogenesis, we summarize the recent advance of GPCRs, especially Class A and F. In particular, the advantages, of zebrafish, which has been widely used in developmental biology as a vertebrate model, are introduced. Using zebrafish will bring the great potential and prospect to demonstrate the role of GPCRs in vascular development in the future.

参考文献

[1] Carmeliet P, Jain RK. Molecular mechanisms and clinical applications of angiogenesis. Nature, 2011, 473 (7347): 298-307.
[2] Adams RH, Alitalo K. Molecular regulation of angiogene-sis and lymphangiogenesis. Nat Rev Mol Cell Biol, 2007, 8(6): 464-478.
[3] You LR, Lin FJ, Lee CT, DeMayo FJ, Tsai MJ, Tsai SY. Suppression of Notch signalling by the COUP-TFII tran-scription factor regulates vein identity. Nature, 2005, 435(7038): 98-104.
[4] Geudens I, Gerhardt H. Coordinating cell behaviour during blood vessel formation. Development, 2011, 138(21): 4569-4583.
[5] Herbert SP, Stainier DY. Molecular control of endothelial cell behaviour during blood vessel morphogenesis. Nat Rev Mol Cell Biol, 2011, 12(9): 551-564.
[6] Krishnan A, Almén MS, Fredriksson R, Schiöth HB. The origin of GPCRs: identification of mammalian like Rhodopsin, Adhesion, Glutamate and Frizzled GPCRs in fungi. PLoS One, 2012, 7(1): e29817.
[7] Liapakis G, Cordomi A, Pardo L. The G-protein coupled receptor family: actors with many faces. Curr Pharm Des, 2012, 18(2): 175-185.
[8] Lappano R, Maggiolini M. G protein-coupled receptors: novel targets for drug discovery in cancer. Nat Rev Drug Discov, 2011, 10(1): 47-60.
[9] Rivera-Lopez CM, Tucker AL, Lynch KR. Lysophos-phatidic acid (LPA) and angiogenesis. Angiogenesis, 2008, 11(3): 301-310.
[10] Liu YJ, Wada R, Yamashita T, Mi YD, Deng CX, Hobson JP, Rosenfeldt HM, Nava VE, Chae SS, Lee MJ, Liu CH, Hla T, Spiegel S, Proia RL. Edg-1, the G protein-coupled receptor for sphingosine-1-phosphate, is essential for vascular maturation. J Clin Invest, 2000, 106(8): 951-961.
[11] Yukiura H, Hama K, Nakanaga K, Tanaka M, Asaoka Y, Okudaira S, Arima N, Inoue A, Hashimoto T, Arai H, Kawahara A, Nishina H, Aoki J. Autotaxin regulates vas-cular development via multiple lysophosphatidic acid (LPA) receptors in Zebrafish. J Biol Chem, 2011, 286(51): 43972-43983.
[12] Contos JJ, Fukushima N, Weiner JA, Kaushal D, Chun J. Requirement for the lpA1 lysophosphatidic acid receptor gene in normal suckling behavior. Proc Natl Acad Sci USA, 2000, 97(24): 13384-13389.
[13] Contos JJ, Ishii I, Fukushima N, Kingsbury MA, Ye X, Kawamura S, Brown JH, Chun J. Characterization of lpa2 (Edg4) and lpa1/lpa2 (Edg2/Edg4) lysophosphatidic acid receptor knockout mice: signaling deficits without obvious phenotypic abnormality attributable to lpa2. Mol Cell Biol, 2002, 22(19): 6921-6929.
[14] Kranenburg O, Poland M, van Horck FP, Drechsel D, Hall A, Moolenaar WH. Activation of RhoA by lysophos-phatidic acid and Gα12/13 subunits in neuronal cells: induc-tion of neurite retraction. Mol Biol Cell, 1999, 10(6): 1851-1857.
[15] Ye XQ, Hama K, Contos JJ, Anliker B, Inoue A, Skinner MK, Suzuki H, Amano T, Kennedy G, Arai H, Aoki J, Chun J. LPA3-mediated lysophosphatidic acid signalling in embryo implantation and spacing. Nature, 2005, 435 (7038): 104-108.
[16] Sumida H, Noguchi K, Kihara Y, Abe M, Yanagida K, Hamano F, Sato S, Tamaki K, Morishita Y, Kano MR, Iwata C, Miyazono K, Sakimura K, Shimizu T, Ishii S. LPA4 regulates blood and lymphatic vessel formation during mouse embryogenesis. Blood, 2010, 116(23): 5060-5070.
[17] Teo ST, Yung YC, Herr DR, Chun J. Lysophosphatidic acid in vascular development and disease. IUBMB Life, 2009, 61(8): 791-799.
[18] Rosen H, Liao JY. Sphingosine 1-phosphate pathway therapeutics: a lipid ligand-receptor paradigm. Curr Opin Chem Biol, 2003, 7(4): 461-468.
[19] Uhlenbrock K, Huber J, Ardati A, Busch AE, Kostenis E. Fluid shear stress differentially regulates gpr3, gpr6, and gpr12 expression in human umbilical vein endothelial cells. Cell Physiol Biochem, 2003, 13(2): 75-84.
[20] Argraves KM, Wilkerson BA, Argraves WS. Sphingos-ine-1-phos
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