Literature DB >> 15238618

Plasticity of mouse renal collecting duct in response to potassium depletion.

Lydie Cheval1, Jean Paul Duong Van Huyen, Patrick Bruneval, Jean-Marc Verbavatz, Jean-Marc Elalouf, Alain Doucet.   

Abstract

Plasticity of mouse renal collecting duct in response to potassium depletion.--Renal collecting ducts are the main sites for regulation of whole body potassium balance. Changes in dietary intake of potassium induce pleiotropic adaptations of collecting duct cells, which include alterations of ion and water transport properties along with an hypertrophic response. To study the pleiotropic adaptation of the outer medullary collecting duct (OMCD) to dietary potassium depletion, we combined functional studies of renal function (ion, water, and acid/base handling), analysis of OMCD hypertrophy (electron microscopy) and hyperplasia (PCNA labeling), and large scale analysis of gene expression (transcriptome analysis). The transcriptome of OMCD was compared in mice fed either a normal or a potassium-depleted diet for 3 days using serial analysis of gene expression (SAGE) adapted for downsized extracts. SAGE is based on the generation of transcript-specific tag libraries. Approximately 20,000 tags corresponding to 10,000 different molecular species were sequenced in each library. Among the 186 tags differentially expressed (P < 0.05) between the two libraries, 120 were overexpressed and 66 were downregulated. The SAGE expression profile obtained in the control library was representative of different functional classes of proteins and of the two cell types (principal and alpha-intercalated cells) constituting the OMCD. Combined with gene expression analysis, results of functional and morphological studies allowed us to identify candidate genes for distinct physiological processes modified by potassium depletion: sodium, potassium, and water handling, hyperplasia and hypertrophy. Finally, comparison of mouse and human OMCD transcriptomes allowed us to address the question of the relevance of the mouse as a model for human physiology and pathophysiology.

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Year:  2004        PMID: 15238618     DOI: 10.1152/physiolgenomics.00055.2004

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   3.107


  9 in total

Review 1.  Global analysis of gene expression in mammalian kidney.

Authors:  Olga Soutourina; Lydie Cheval; Alain Doucet
Journal:  Pflugers Arch       Date:  2004-12-21       Impact factor: 3.657

2.  NBCe1-A is required for the renal ammonia and K+ response to hypokalemia.

Authors:  Hyun-Wook Lee; Autumn N Harris; Michael F Romero; Paul A Welling; Charles S Wingo; Jill W Verlander; I David Weiner
Journal:  Am J Physiol Renal Physiol       Date:  2019-12-16

3.  Discovery of genes related to diabetic nephropathy in various animal models by current techniques.

Authors:  Jun Wada; Lin Sun; Yashpal S Kanwar
Journal:  Contrib Nephrol       Date:  2011-01-20       Impact factor: 1.580

Review 4.  The Rh protein family: gene evolution, membrane biology, and disease association.

Authors:  Cheng-Han Huang; Mao Ye
Journal:  Cell Mol Life Sci       Date:  2009-12-02       Impact factor: 9.261

5.  H,K-ATPase type 2 contributes to salt-sensitive hypertension induced by K(+) restriction.

Authors:  Christine Walter; Mariem Ben Tanfous; Katia Igoudjil; Amel Salhi; Geneviève Escher; Gilles Crambert
Journal:  Pflugers Arch       Date:  2016-08-25       Impact factor: 3.657

6.  GDF15 triggers homeostatic proliferation of acid-secreting collecting duct cells.

Authors:  Jean Paul Duong Van Huyen; Lydie Cheval; May Bloch-Faure; Marie France Belair; Didier Heudes; Patrick Bruneval; Alain Doucet
Journal:  J Am Soc Nephrol       Date:  2008-07-23       Impact factor: 10.121

7.  Of mice and men: divergence of gene expression patterns in kidney.

Authors:  Lydie Cheval; Fabien Pierrat; Rabary Rajerison; David Piquemal; Alain Doucet
Journal:  PLoS One       Date:  2012-10-03       Impact factor: 3.240

8.  Dissecting the Effects of Aldosterone and Hypokalemia on the Epithelial Na+ Channel and the NaCl Cotransporter.

Authors:  Mathias Kristensen; Robert A Fenton; Søren B Poulsen
Journal:  Front Physiol       Date:  2022-04-26       Impact factor: 4.755

9.  The serine-threonine kinase PIM3 is an aldosterone-regulated protein in the distal nephron.

Authors:  Alessia Spirli; Lydie Cheval; Anne Debonneville; David Penton; Caroline Ronzaud; Marc Maillard; Alain Doucet; Johannes Loffing; Olivier Staub
Journal:  Physiol Rep       Date:  2019-08
  9 in total

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