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2.
Am J Physiol Renal Physiol ; 291(1): F218-24, 2006 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-16478974

RESUMEN

To identify novel gene targets of vasopressin regulation in the renal medulla, we performed a cDNA microarray study on the inner medullary tissue of mice following a 48-h water restriction protocol. In this study, 4,625 genes of the possible approximately 12,000 genes on the array were included in the analysis, and of these 157 transcripts were increased and 63 transcripts were decreased by 1.5-fold or more. Quantitative, real-time PCR measurements confirmed the increases seen for 12 selected transcripts, and the decreases were confirmed for 7 transcripts. In addition, we measured transcript abundance for many renal collecting duct proteins that were not represented on the array; aquaporin-2 (AQP2), AQP3, Pax-8, and alpha- and beta-Na-K-ATPase subunits were all significantly increased in abundance; the beta- and gamma-subunits of ENaC and the vasopressin type 1A receptor were significantly decreased. To correlate changes in mRNA expression with changes in protein expression, we carried out quantitative immunoblotting. For most of the genes examined, changes in mRNA abundances were not associated with concomitant protein abundance changes; however, AQP2 transcript abundance and protein abundance did correlate. Surprisingly, aldolase B transcript abundance was increased but protein abundance was decreased following 48 h of water restriction. Several transcripts identified by microarray were novel with respect to their expression in mouse renal medullary tissues. The steroid hormone enzyme 3beta-hydroxysteroid dehydrogenase 4 (3betaHSD4) was identified as a novel target of vasopressin regulation, and via dual labeling immunofluorescence we colocalized the expression of this protein to AQP2-expressing collecting ducts of the kidney. These studies have identified several transcripts whose abundances are regulated in mouse inner medulla in response to an increase in endogenous vasopressin levels and could play roles in the regulation of salt and water excretion.


Asunto(s)
3-Hidroxiesteroide Deshidrogenasas/análisis , 3-Hidroxiesteroide Deshidrogenasas/genética , Regulación Enzimológica de la Expresión Génica/fisiología , Médula Renal/química , Túbulos Renales Colectores/química , Privación de Agua/fisiología , Animales , Acuaporina 2/análisis , Acuaporina 2/genética , Acuaporina 2/fisiología , Acuaporina 3/análisis , Acuaporina 3/genética , Acuaporina 3/fisiología , ADN Complementario/análisis , Canales Epiteliales de Sodio , Fructosa-Bifosfato Aldolasa/análisis , Fructosa-Bifosfato Aldolasa/genética , Fructosa-Bifosfato Aldolasa/fisiología , Médula Renal/fisiología , Túbulos Renales Colectores/fisiología , Ratones , Ratones Endogámicos ICR , Análisis de Secuencia por Matrices de Oligonucleótidos , Factor de Transcripción PAX8 , Factores de Transcripción Paired Box/análisis , Factores de Transcripción Paired Box/genética , Factores de Transcripción Paired Box/fisiología , ARN Mensajero/análisis , Receptores de Vasopresinas/análisis , Receptores de Vasopresinas/genética , Receptores de Vasopresinas/fisiología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Canales de Sodio/análisis , Canales de Sodio/genética , Canales de Sodio/fisiología , ATPasa Intercambiadora de Sodio-Potasio/análisis , ATPasa Intercambiadora de Sodio-Potasio/genética , ATPasa Intercambiadora de Sodio-Potasio/fisiología , Vasopresinas/sangre , Vasopresinas/fisiología
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