The molecular basis of embryonic kidney development
- PMID: 9152004
- DOI: 10.1016/s0925-4773(97)00667-9
The molecular basis of embryonic kidney development
Abstract
The development of the mature mammalian kidney begins with the invasion of metanephric mesenchyme by ureteric bud. Mesenchymal cells near the bud become induced and convert to an epithelium which goes on to generate the functional filtering unit of the kidney, the nephron. The collecting duct system is elaborated by the branching ureter, the growth of which is dependent upon signals from the metanephric mesenchyme. The process of reciprocal induction between ureter and mesenchyme is repeated many times over during development and is the key step in generating the overall architecture of the kidney. Genetic studies in mice have allowed researchers to begin to unravel the molecular signals that govern these early events. These experiments have revealed that a number of essential gene products are required for distinct steps in kidney organogenesis. Here we review and summarize the developmental role played by some of these molecules, especially certain transcription factors and growth factors and their receptors. Although the factors involved are far from completely known a rough framework of a molecular cascade which governs embryonic kidney development is beginning to emerge.
Similar articles
-
Wnt11 and Ret/Gdnf pathways cooperate in regulating ureteric branching during metanephric kidney development.Development. 2003 Jul;130(14):3175-85. doi: 10.1242/dev.00520. Development. 2003. PMID: 12783789
-
Regulation of ureteric bud outgrowth by Pax2-dependent activation of the glial derived neurotrophic factor gene.Development. 2001 Dec;128(23):4747-56. doi: 10.1242/dev.128.23.4747. Development. 2001. PMID: 11731455
-
Glial cell line-derived neurotrophic factor stimulates ureteric bud outgrowth and enhances survival of ureteric bud cells in vitro.Exp Nephrol. 1998 Jul-Aug;6(4):337-51. doi: 10.1159/000020541. Exp Nephrol. 1998. PMID: 9690097
-
[Renal development and its molecular mechanism].Tanpakushitsu Kakusan Koso. 2005 May;50(6 Suppl):644-9. Tanpakushitsu Kakusan Koso. 2005. PMID: 15926494 Review. Japanese. No abstract available.
-
The tip-top branching ureter.Curr Opin Cell Biol. 1997 Dec;9(6):877-84. doi: 10.1016/s0955-0674(97)80091-9. Curr Opin Cell Biol. 1997. PMID: 9425354 Review.
Cited by
-
Aquaporin 2 promotes cell migration and epithelial morphogenesis.J Am Soc Nephrol. 2012 Sep;23(9):1506-17. doi: 10.1681/ASN.2012010079. Epub 2012 Aug 2. J Am Soc Nephrol. 2012. PMID: 22859853 Free PMC article.
-
GDNF: a novel factor with therapeutic potential for neurodegenerative disorders.Mol Neurobiol. 1999 Feb;19(1):43-59. doi: 10.1007/BF02741377. Mol Neurobiol. 1999. PMID: 10321971
-
Bim gene dosage is critical in modulating nephron progenitor survival in the absence of microRNAs during kidney development.FASEB J. 2017 Aug;31(8):3540-3554. doi: 10.1096/fj.201700010R. Epub 2017 Apr 26. FASEB J. 2017. PMID: 28446592 Free PMC article.
-
PAX2 loss by immunohistochemistry occurs early and often in endometrial hyperplasia.Int J Gynecol Pathol. 2012 Mar;31(2):151-159. doi: 10.1097/PGP.0b013e318226b376. Int J Gynecol Pathol. 2012. PMID: 22317873 Free PMC article.
-
Deregulated expression of the homeobox gene Cux-1 in transgenic mice results in downregulation of p27(kip1) expression during nephrogenesis, glomerular abnormalities, and multiorgan hyperplasia.Dev Biol. 2002 May 1;245(1):157-71. doi: 10.1006/dbio.2002.0636. Dev Biol. 2002. PMID: 11969263 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases