Literature DB >> 15465493

Expression of Hairy/Enhancer of Split genes, Hes1 and Hes5, during murine nephron morphogenesis.

Tino D Piscione1, Megan Y J Wu, Susan E Quaggin.   

Abstract

Hairy/Enhancer of Split (Hes) genes encode transcriptional repressors that function as downstream targets of activated Notch receptors in cell fate decisions during tissue development. During nephrogenesis, multiple Notch pathway genes are co-expressed in multi-potent epithelial progenitors (i.e. pre-tubular aggregates), but demonstrate distinct expression patterns in early nephrons (i.e. S-shaped bodies), suggesting that Notch signaling functions in patterning epithelial cell fate during nephron morphogenesis. To define the spatial activation of the Notch pathway in developing nephrons, we analyzed the expression of Hes1 and Hes5 by mRNA in situ hybridization in cryosections of developing kidneys, and compared their spatiotemporal expression with the expression of other Notch pathway genes in nephron progenitors. Hes1, and to a lesser extent Hes5, were expressed in pre-tubular aggregates and comma-shaped bodies of embryonic day (E) 13.5 and newborn kidneys. In S-shaped bodies, Hes1 expression was detected in the middle part which gives rise to the proximal tubule, but also extended into the lower and upper parts which give rise to the glomerulus and distal tubule, respectively, and was similar to the proximal-distal expression patterns for Notch1 and Jagged1 in these nephrogenic structures. In contrast, strong Hes5 expression was restricted to the middle segment of S-shaped bodies, and resembled Delta-like 1 expression. These data show that Hes1 and Hes5 expression are independently regulated along the proximal-distal axis of the developing nephron. Consequently, the differential, spatial regulation of Hes1 and Hes5 gene expression by the Notch signaling pathway in developing nephrons may be a mechanism for patterning cell fate decisions during nephron morphogenesis.

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Year:  2004        PMID: 15465493     DOI: 10.1016/j.modgep.2004.04.007

Source DB:  PubMed          Journal:  Gene Expr Patterns        ISSN: 1567-133X            Impact factor:   1.224


  39 in total

1.  Expression of Notch pathway proteins correlates with albuminuria, glomerulosclerosis, and renal function.

Authors:  Mariana Murea; Jun-Ki Park; Shuchita Sharma; Hideki Kato; Antje Gruenwald; Thiruvur Niranjan; Han Si; David B Thomas; James M Pullman; Michal L Melamed; Katalin Susztak
Journal:  Kidney Int       Date:  2010-06-09       Impact factor: 10.612

2.  The fate of Notch-deficient nephrogenic progenitor cells during metanephric kidney development.

Authors:  Ramon G B Bonegio; Laurence H Beck; Roopkiranjot K Kahlon; Weining Lu; David J Salant
Journal:  Kidney Int       Date:  2011-01-26       Impact factor: 10.612

3.  Maternal undernourished fetal kidneys exhibit differential regulation of nephrogenic genes including downregulation of the Notch signaling pathway.

Authors:  Thomas R Magee; Sanaz A Tafti; Mina Desai; Qinghai Liu; Michael G Ross; Cynthia C Nast
Journal:  Reprod Sci       Date:  2011-01-27       Impact factor: 3.060

Review 4.  Notch in the kidney: development and disease.

Authors:  Yasemin Sirin; Katalin Susztak
Journal:  J Pathol       Date:  2011-08-24       Impact factor: 7.996

Review 5.  Notch signaling in human development and disease.

Authors:  Andrea L Penton; Laura D Leonard; Nancy B Spinner
Journal:  Semin Cell Dev Biol       Date:  2012-01-28       Impact factor: 7.727

6.  Notch2, but not Notch1, is required for proximal fate acquisition in the mammalian nephron.

Authors:  Hui-Teng Cheng; Mijin Kim; M Todd Valerius; Kameswaran Surendran; Karin Schuster-Gossler; Achim Gossler; Andrew P McMahon; Raphael Kopan
Journal:  Development       Date:  2007-01-17       Impact factor: 6.868

Review 7.  Molecular insights into segmentation along the proximal-distal axis of the nephron.

Authors:  Raphael Kopan; Hui-Teng Cheng; Kameswaran Surendran
Journal:  J Am Soc Nephrol       Date:  2007-06-13       Impact factor: 10.121

8.  Notch2 activation in the embryonic kidney depletes nephron progenitors.

Authors:  Sayoko Fujimura; Qing Jiang; Chiyoko Kobayashi; Ryuichi Nishinakamura
Journal:  J Am Soc Nephrol       Date:  2010-03-18       Impact factor: 10.121

9.  The prepattern transcription factor Irx3 directs nephron segment identity.

Authors:  Luca Reggiani; Daniela Raciti; Rannar Airik; Andreas Kispert; André W Brändli
Journal:  Genes Dev       Date:  2007-09-15       Impact factor: 11.361

Review 10.  The pathogenic role of Notch activation in podocytes.

Authors:  Thiruvur Niranjan; Mariana Murea; Katalin Susztak
Journal:  Nephron Exp Nephrol       Date:  2009-03-17
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