Regulation by aldosterone of Na+,K+-ATPase mRNAs, protein synthesis, and sodium transport in cultured kidney cells.
Details
State: Public
Version: Final published version
License: CC BY-NC-SA 4.0
Serval ID
serval:BIB_C1D503E9BA0E
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Regulation by aldosterone of Na+,K+-ATPase mRNAs, protein synthesis, and sodium transport in cultured kidney cells.
Journal
The Journal of cell biology
ISSN
0021-9525
Publication state
Published
Issued date
1987
Peer-reviewed
Oui
Volume
104
Number
5
Pages
1231-7
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't - Publication Status: ppublish
Abstract
Transepithelial Na+ reabsorption across tight epithelia is regulated by aldosterone. Mineralocorticoids modulate the expression of a number of proteins. Na+,K+-ATPase has been identified as an aldosterone-induced protein (Geering, K., M. Girardet, C. Bron, J. P. Kraehenbuhl, and B. C. Rossier, 1982, J. Biol. Chem., 257:10338-10343). Using A6 cells (kidney of Xenopus laevis) grown on filters we demonstrated by Northern blot analysis that the induction of Na+,K+-ATPase was mainly mediated by a two- to fourfold accumulation of both alpha- and beta-subunit mRNAs. The specific competitor spironolactone decreased basal Na+ transport, Na+,K+-ATPase mRNA, and the relative rate of protein biosynthesis, and it blocked the response to aldosterone. Cycloheximide inhibited the aldosterone-dependent sodium transport but did not significantly affect the cytoplasmic accumulation of Na+,K+-ATPase mRNA induced by aldosterone.
Keywords
Aldosterone, Animals, Biological Transport, Active, Cell Line, Cycloheximide, Kidney, Macromolecular Substances, Nucleic Acid Hybridization, Protein Biosynthesis, RNA, Messenger, Sodium, Sodium-Potassium-Exchanging ATPase, Xenopus laevis
Pubmed
Web of science
Open Access
Yes
Create date
24/01/2008 14:00
Last modification date
20/08/2019 16:36
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