AJP - Renal AJP: Cell Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Am J Physiol Renal Physiol (April 23, 2008). doi:10.1152/ajprenal.90245.2008
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Google Scholar
Right arrow Articles by McDonald, F. J
PubMed
Right arrow PubMed Citation
Right arrow Articles by McDonald, F. J
Submitted on April 10, 2008
Revised on April 16, 2008
Accepted on April 17, 2008

A new SGK1 knockout mouse

Fiona J McDonald1*

1 University of Otago

* To whom correspondence should be addressed. E-mail: fiona.mcdonald{at}stonebow.otago.ac.nz.

The Serum and Glucocorticoid regulated Kinase (SGK1) is a component of the pathway mediating activation of the epithelial sodium channel, ENaC, in the aldosterone-sensitive distal nephron (ASDN). Two knockout mouse models for SGK1 have now been described. On a low salt diet salt wasting is observed in both models, but decreased ENaC activity is reported in the collecting ducts of one model while an increase was observed in the new model. The abundance of the Na+ Cl- cotransporter is suggested to be decreased in the absence of SGK1 in the new model. Further, the new paper reports that SGK1 is not needed for chronic aldosterone stimulation of ENaC, and that lack of SGK1 reduces the processing of the {gamma}ENaC protein to a 65 kDa form.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Visit Other APS Journals Online
Copyright © 1977 by the American Physiological Society.