肾脏发育中信号通路的调控作用

doi:10.16288/j.yczz.2015.01.001

遗传 ›› 2015, Vol. 37 ›› Issue (1): 1-7.doi: 10.16288/j.yczz.2015.01.001

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肾脏发育中信号通路的调控作用

邱晓^{1, 2}, 韦荣飞^{1, 2}, 张令强², 贺福初^{1, 2}

1. 清华大学生命科学学院,北京 100089;
2. 军事医学科学院放射与辐射医学研究所,蛋白质组学国家重点实验室,北京 100850

收稿日期:2014-07-26 修回日期:2014-10-15 出版日期:2015-01-20 发布日期:2015-01-20
通讯作者: 张令强,研究员,研究方向：蛋白质泛素化修饰与疾病。E-mail: zhanglq550@163.com E-mail:zhanglq550@163.com
作者简介:邱晓,在读博士研究生,研究方向：细胞生物学。E-mail: sdsqiuxiao378@126.com韦荣飞,在读博士研究生,研究方向：细胞生物学。E-mail: weirongfei2010@163.com
基金资助:
国家自然科学基金项目(编号：31125010,31471364)和重大科学研究计划课题部分项目(编号：2012CB910304,2011CB910602)资助

The roles of signaling pathways in regulating kidney development

Xiao Qiu^{1, 2}, Rongfei Wei^{1, 2}, Lingqiang Zhang², Fuchu He^{1, 2}

1. School of Life Sciences, Tsinghua University, Beijing 100089, China; 2. State Key Laboratory of Proteomics, Beijing Institute of Radiation Medicine, Beijing 100850, China

Received:2014-07-26 Revised:2014-10-15 Online:2015-01-20 Published:2015-01-20

摘要/Abstract

摘要： 肾脏发育是一个复杂的过程,需要在输尿管芽细胞和基质细胞相互诱导下,引起细胞生长、增殖、分化,从而产生肾单位及各种管状结构,最终发育为成熟的肾脏。在肾脏发育过程中,GDNF/Ret、Wnt、BMP等一系列信号通路参与了发育的调控过程。这些信号通路在肾脏发育的不同阶段或不同位置发挥着重要的调控作用,并且通路之间存在相互的调控,从而形成了一个复杂而精细的调控网络,保证了肾脏的正常发育。文章概括了肾脏发育的过程,总结了肾脏发育过程中相关信号通路对肾脏发育的调控作用以及信号通路之间的相互调控。

关键词: 肾脏发育, GDNF/Ret, Wnt, BMP, FGF, Notch

Abstract: The development of mammalian kidney is a complex process. The reciprocal inductive interactions between epithelial cells and metanephric mesenchymal cells determine cell fates including proliferation, growth, apoptosis, and eventually contribute to the formation of an intact kidney. Multiple signaling pathways, including the GDNF/Ret, Wnt and BMP signaling pathways, have been shown to regulate the development of kidney. A myriad of signaling pathways and their cross-talks form a precise spatiotemporal regulatory network, which ensures the kidney to be properly organized. In this review, we summarize the physiological process of kidney development as well as the involved signaling pathways and their interplay.

Key words: kidney development, GDNF/Ret, Wnt, BMP, FGF, Notch

邱晓, 韦荣飞, 张令强, 贺福初. 肾脏发育中信号通路的调控作用[J]. 遗传, 2015, 37(1): 1-7.

Xiao Qiu, Rongfei Wei, Lingqiang Zhang, Fuchu He. The roles of signaling pathways in regulating kidney development[J]. HEREDITAS(Beijing), 2015, 37(1): 1-7.

参考文献

[1] Chai OH, Song CH, Park SK, Kim W, Cho ES. Molecular regulation of kidney development. Anat Cell Biol , 2013, 46(1): 19-31.
[2] Patel SR, Dressler GR. The genetics and epigenetics of kidney development. Semin Nephrol , 2013, 33(4): 314-326.
[3] Faa G, Gerosa C, Fanni D, Monga G, Zaffanello M, Van Eyken P, Fanos V. Morphogenesis and molecular mechanisms involved in human kidney development. J Cell Physiol , 2012, 227(3): 1257-1268.
[4] Dressler GR. The cellular basis of kidney development. Annu Rev Cell Dev Biol , 2006, 22: 509-529.
[5] Sequeira Lopez MLS, Gomez RA. Development of the renal arterioles. J Am Soc Nephrol , 2011, 22(12): 2156-2165.
[6] Davis TK, Hoshi M, Jain S. To bud or not to bud: the RET perspective in CAKUT. Pediatr Nephrol , 2014, 29(4): 597- 608.
[7] Schuchardt A, D'Agati V, Larsson-Blomberg L, Costantini F, Pachnis V. Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature , 1994, 367(6461): 380-383.
[8] Pichel JG, Shen L, Sheng HZ, Granholm AC, Drago J, Grinberg A, Lee EJ, Huang SP, Saarma M, Hoffer BJ, Sariola H, Westphal H. Defects in enteric innervation and kidney development in mice lacking GDNF. Nature , 1996, 382(6586): 73-76.
[9] Chi X, Michos O, Shakya R, Riccio P, Enomoto H, Licht JD, Asai N, Takahashi M, Ohgami N, Kato M, Mendelsohn C, Costantini F. Ret-dependent cell rearrangements in the Wolffian duct epithelium initiate ureteric bud morphogenesis. Dev Cell , 2009, 17(2): 199-209.
[10] Hoshi M, Batourina E, Mendelsohn C, Jain S. Novel mechanisms of early upper and lower urinary tract patterning regulated by RetY1015 docking tyrosine in mice. Development , 2012, 139(13): 2405-2415.
[11] Costantini F. GDNF/Ret signaling and renal branching morphogenesis: From mesenchymal signals to epithelial cell behaviors. Organogenesis , 2010, 6(4): 252-262.
[12] Tang MJ, Cai Y, Tsai SJ, Wang YK, Dressler GR. Ureteric bud outgrowth in response to RET activation is mediated by phosphatidylinositol 3-kinase. Dev Biol, 2002, 243(1): 128-136.
[13] Yang YZ. Wnt signaling in development and disease. Cell Biosci , 2012, 2(1): 14.
[14] Freese JL, Pino D, Pleasure SJ. Wnt signaling in development and disease. Neurobiol Dis , 2010, 38(2): 148-153.
[15] Stark K, Vainio S, Vassileva G, McMahon AP. Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4. Nature , 1994, 372(6507): 679-683.
[16] Carroll TJ, Park JS, Hayashi S, Majumdar A, McMahon AP. Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system. Dev Cell , 2005, 9(2): 283-292.
[17] Park JS, Valerius MT, McMahon AP. Wnt/β-catenin signaling regulates nephron induction during mouse kidney development. Development , 2007, 134(13): 2533-2539.
[18] Fischer E, Legue E, Doyen A, Nato F, Nicolas JF, Torres V, Yaniv M, Pontoglio M. Defective planar cell polarity in polycystic kidney disease. Nat Genet , 2006, 38(1): 21-23.
[19] Karner CM, Chirumamilla R, Aoki S, Igarashi P, Wallingford JB, Carroll TJ. Wnt9b signaling regulates planar cell polarity and kidney tubule morphogenesis. Nat Genet , 2009, 41(7): 793-799.
[20] Yu J, Carroll TJ, Rajagopal J, Kobayashi A, Ren Q, McMahon AP. A Wnt7b-dependent pathway regulates the orientation of epithelial cell division and establishes the cortico-medullary axis of the mammalian kidney. Development , 2009, 136(1): 161-171.
[21] Oxburgh L, Brown AC, Muthukrishnan SD, Fetting JL. Bone morphogenetic protein signaling in nephron progenitor cells. Pediat Nephrol , 2014, 29(4): 531-536.
[22] Pope JC 4th, Brock JW 3rd, Adams MC, Stephens FD, Ichikawa I. How they begin and how they end: classic and new theories for the development and deterioration of congenital anomalies of the kidney and urinary tract, CAKUT. J Am Soc Nephrol , 1999, 10(9): 2018-2028.
[23] Dudley AT, Lyons KM, Robertson EJ. A requirement for bone morphogenetic protein-7 during development of the mammalian kidney and eye. Genes Dev , 1995, 9(22): 2795-2807.
[24] Winnier G, Blessing M, Labosky PA, Hogan BL. Bone morphogenetic protein-4 is required for mesoderm formation and patterning in the mouse. Genes Dev , 1995, 9(17): 2105-2116.
[25] Tomita M, Asada M, Asada N, Nakamura J, Oguchi A, Higashi AY, Endo S, Robertson E, Kimura T, Kita T, Economides AN, Kreidberg J, Yanagita M. Bmp7 maintains undifferentiated kidney progenitor population and determines nephron numbers at birth. PLoS One , 2013, 8(8): e73554.
[26] Trueb B, Amann R, Gerber SD. Role of FGFRL1 and other FGF signaling proteins in early kidney development. Cell Mol Life Sci , 2013, 70(14): 2505-2518.
[27] Tsang M, Dawid IB. Promotion and attenuation of FGF signaling through the Ras-MAPK pathway. Sci STKE , 2004, 2004(228): pe17.
[28] Qiao J, Bush KT, Steer DL, Stuart RO, Sakurai H, Wachsman W, Nigam SK. Multiple fibroblast growth factors support growth of the ureteric bud but have different effects on branching morphogenesis. Mech Dev , 2001, 109(2): 123-135.
[29] Ohuchi H, Hori Y, Yamasaki M, Harada H, Sekine K, Kato S, Itoh N. FGF10 acts as a major ligand for FGF receptor 2 IIIb in mouse multi-organ development. Biochem Biophys Res Commun , 2000, 277(3): 643-649.
[30] De Moerlooze L, Spencer-Dene B, Revest JM, Hajihosseini M, Rosewell I, Dickson C. An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis. Development , 2000, 127(3): 483-492.
[31] Barak H, Huh SH, Chen S, Jeanpierre C, Martinovic J, Parisot M, Bole-Feysot C, Nitschke P, Salomon R, Antignac C, Ornitz DM, Kopan R. FGF9 and FGF20 maintain the stemness of nephron progenitors in mice and man. Dev Cell , 2012, 22(6): 1191-1207.
[32] Grieshammer U, Cebrian C, Ilagan R, Meyers E, Herzlinger D, Martin GR. FGF8 is required for cell survival at distinct stages of nephrogenesis and for regulation of gene expression in nascent nephrons. Development , 2005, 132(17): 3847-3857.
[33] Wang P, Pereira FA, Beasley D, Zheng H. Presenilins are required for the formation of comma- and S-shaped bodies during nephrogenesis. Development , 2003, 130(20): 5019- 5029.
[34] Jeong HW, Jeon US, Koo BK, Kim WY, Im SK, Shin J, Cho Y, Kim J, Kong YY. Inactivation of Notch signaling in the renal collecting duct causes nephrogenic diabetes insipidus in mice. J Clin Invest , 2009, 119(11): 3290-3300.
[35] Boyle SC, Liu ZY, Kopan R. Notch signaling is required for the formation of mesangial cells from a stromal mesenchyme precursor during kidney development. Development , 2014, 141(2): 346-354.
[36] Yu J, Carroll TJ, McMahon AP. Sonic hedgehog regulates proliferation and differentiation of mesenchymal cells in the mouse metanephric kidney. Development , 2002, 129(22): 5301-5312.
[37] Zhang X, Mernaugh G, Yang DH, Gewin L, Srichai MB, Harris RC, Iturregui JM, Nelson RD, Kohan DE, Abrahamson D, Fassler R, Yurchenco P, Pozzi A, Zent R. β1 integrin is necessary for ureteric bud branching morphogenesis and maintenance of collecting duct structural integrity. Development , 2009, 136(19): 3357-3366.
[38] Pepicelli CV, Kispert A, Rowitch DH, McMahon AP. GDNF induces branching and increased cell proliferation in the ureter of the mouse. Dev Biol , 1997, 192(1): 193-198.
[39] Majumdar A, Vainio S, Kispert A, McMahon J, McMahon AP. Wnt11 and Ret/Gdnf pathways cooperate in regulating ureteric branching during metanephric kidney development. Development , 2003, 130(14): 3175-3185.
[40] Michos O, Goncalves A, Lopez-Rios J, Tiecke E, Naillat F, Beier K, Galli A, Vainio S, Zeller R. Reduction of BMP4 activity by gremlin 1 enables ureteric bud outgrowth and GDNF/WNT11 feedback signalling during kidney branching morphogenesis. Development , 2007, 134(13): 2397-2405.
[41] Michos O, Cebrian C, Hyink D, Grieshammer U, Williams L, D'Agati V, Licht JD, Martin GR, Costantini F. Kidney development in the absence of Gdnf and Spry1 requires Fgf10 . PLoS Genetics , 2010, 6(1): e1000809.
[42] Nishita M, Qiao S, Miyamoto M, Okinaka Y, Yamada M, Hashimoto R, Iijima K, Otani H, Hartmann C, Nishinakamura R, Minami Y. Role of Wnt5a-Ror2 signaling in morphogenesis of the metanephric mesenchyme during ureteric budding. Mol Cell Biol , 2014, 34(16): 3096-3105.
[43] Herr F, Schreiner I, Baal N, Pfarrer C, Zygmunt M. Expression patterns of Notch receptors and their ligands Jagged and Delta in human placenta. Placenta , 2011, 32(8): 554-563.

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肾脏发育中信号通路的调控作用

The roles of signaling pathways in regulating kidney development

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