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Am J Physiol Renal Physiol 289: F451-F458, 2005. First published March 29, 2005; doi:10.1152/ajprenal.00376.2004
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Regulated expression of renal and intestinal UT-B urea transporter in response to varying urea load

Hideki Inoue,1 Shelley D. Kozlowski,2 Janet D. Klein,2 James L. Bailey,2 Jeff M. Sands,2 and Serena M. Bagnasco1

1Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland; and 2Renal Division, Department of Medicine, Emory University School of Medicine, Atlanta Georgia

Submitted 8 October 2004 ; accepted in final form 24 March 2005

Production, recycling, and elimination of urea are important to maintain nitrogen balance. Adaptation to varying loads of urea due to different protein intake or in renal failure may involve changes in urea transport and may possibly affect urea transporters. In this study, we examined the expression of the UT-B urea transporter in rats fed a low-protein diet (LPD), a high-protein diet (HPD), and a 20% urea-supplemented diet. In the kidney, UT-B protein abundance increased in the outer medulla of both LPD-fed rats and 20% urea-fed rats, without changes in the inner medulla of either group compared with controls. In HPD-fed rats, UT-B protein decreased significantly in both the outer and inner medulla. We identified expression of UT-B in the rat colon, as a 2-kb mRNA transcript and as an ~45-kDa protein, with apical localization in superficial colon epithelial cells. UT-B also is expressed in rat small intestine. In rat colon, UT-B protein abundance was mildly, but significantly, decreased in LPD-fed and 20% urea-fed rats. UT-B abundance also was examined in the colon of 7/8 nephrectomized, uremic rats and in HPD-fed rats and was not significantly different from that in control rats. These findings indicate that UT-B expression is regulated in response to different loads of urea, with a pattern that suggests involvement of tissue-specific regulatory mechanism in kidney and colon.

kidney; urea transport; colon; uremia



Address for reprint requests and other correspondence: S. M. Bagnasco, Dept. of Pathology, Johns Hopkins Hospital, 600 North Wolfe St., Baltimore, MD 21287 (E-mail: sbagnas1{at}jhmi.edu)




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