Wt-1 Expression Linked to Nitric Oxide Availability during Neonatal Obstructive Nephropathy

The wt-1 gene encodes a zinc finger DNA-binding protein that acts as a transcriptional activator or repressor depending on the cellular or chromosomal context. The wt-1 regulates the expression of a large number of genes that have a critical role in kidney development. Congenital obstructive nephrop...

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Main Authors: Luciana Mazzei, Walter Manucha
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:Advances in Urology
Online Access:http://dx.doi.org/10.1155/2013/401750
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spelling doaj-ca9c8c47333c4c3b8fb3a8d21d2e22c12020-11-25T00:52:30ZengHindawi LimitedAdvances in Urology1687-63691687-63772013-01-01201310.1155/2013/401750401750Wt-1 Expression Linked to Nitric Oxide Availability during Neonatal Obstructive NephropathyLuciana Mazzei0Walter Manucha1Área de Fisiopatología, Departamento de Patología, Facultad de Ciencias Médicas, Universidad Nacional de Cuyo, Centro Universitario, CP 5500, Mendoza, ArgentinaÁrea de Fisiopatología, Departamento de Patología, Facultad de Ciencias Médicas, Universidad Nacional de Cuyo, Centro Universitario, CP 5500, Mendoza, ArgentinaThe wt-1 gene encodes a zinc finger DNA-binding protein that acts as a transcriptional activator or repressor depending on the cellular or chromosomal context. The wt-1 regulates the expression of a large number of genes that have a critical role in kidney development. Congenital obstructive nephropathy disrupts normal renal development and causes chronic progressive interstitial fibrosis, which contributes to renal growth arrest, ultimately leading to chronic renal failure. Wt-1 is downregulated during congenital obstructive nephropathy, leading to apoptosis. Of great interest, nitric oxide bioavailability associated with heat shock protein 70 (Hsp70) interaction may modulate wt-1 mRNA expression, preventing obstruction-induced cell death during neonatal unilateral ureteral obstruction. Moreover, recent genetic researches have allowed characterization of many of the complex interactions among the individual components cited, but the realization of new biochemical, molecular, and functional experiments as proposed in our and other research labs allows us to establish a deeper level of commitment among proteins involved and the potential pathogenic consequences of their imbalance.http://dx.doi.org/10.1155/2013/401750
collection DOAJ
language English
format Article
sources DOAJ
author Luciana Mazzei
Walter Manucha
spellingShingle Luciana Mazzei
Walter Manucha
Wt-1 Expression Linked to Nitric Oxide Availability during Neonatal Obstructive Nephropathy
Advances in Urology
author_facet Luciana Mazzei
Walter Manucha
author_sort Luciana Mazzei
title Wt-1 Expression Linked to Nitric Oxide Availability during Neonatal Obstructive Nephropathy
title_short Wt-1 Expression Linked to Nitric Oxide Availability during Neonatal Obstructive Nephropathy
title_full Wt-1 Expression Linked to Nitric Oxide Availability during Neonatal Obstructive Nephropathy
title_fullStr Wt-1 Expression Linked to Nitric Oxide Availability during Neonatal Obstructive Nephropathy
title_full_unstemmed Wt-1 Expression Linked to Nitric Oxide Availability during Neonatal Obstructive Nephropathy
title_sort wt-1 expression linked to nitric oxide availability during neonatal obstructive nephropathy
publisher Hindawi Limited
series Advances in Urology
issn 1687-6369
1687-6377
publishDate 2013-01-01
description The wt-1 gene encodes a zinc finger DNA-binding protein that acts as a transcriptional activator or repressor depending on the cellular or chromosomal context. The wt-1 regulates the expression of a large number of genes that have a critical role in kidney development. Congenital obstructive nephropathy disrupts normal renal development and causes chronic progressive interstitial fibrosis, which contributes to renal growth arrest, ultimately leading to chronic renal failure. Wt-1 is downregulated during congenital obstructive nephropathy, leading to apoptosis. Of great interest, nitric oxide bioavailability associated with heat shock protein 70 (Hsp70) interaction may modulate wt-1 mRNA expression, preventing obstruction-induced cell death during neonatal unilateral ureteral obstruction. Moreover, recent genetic researches have allowed characterization of many of the complex interactions among the individual components cited, but the realization of new biochemical, molecular, and functional experiments as proposed in our and other research labs allows us to establish a deeper level of commitment among proteins involved and the potential pathogenic consequences of their imbalance.
url http://dx.doi.org/10.1155/2013/401750
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AT waltermanucha wt1expressionlinkedtonitricoxideavailabilityduringneonatalobstructivenephropathy
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