Literature DB >> 20592712

Adaptation to metabolic acidosis and its recovery are associated with changes in anion exchanger distribution and expression in the cortical collecting duct.

Jeffrey M Purkerson1, Shuichi Tsuruoka, D Zachary Suter, Aya Nakamori, George J Schwartz.   

Abstract

It is well known that acid/base disturbances modulate proton/bicarbonate transport in the cortical collecting duct. To study the adaptation further we measured the effect of three days of acidosis followed by the rapid recovery from this acidosis on the number and type of intercalated cells in the rabbit cortical collecting duct. Immunofluorescence was used to determine the expression of apical pendrin in β-intercalated cells and the basolateral anion exchanger (AE1) in α-intercalated cells. Acidosis resulted in decreased bicarbonate and increased proton secretion, which correlated with reduced pendrin expression and the number of pendrin-positive cells, as well as decreased pendrin mRNA and protein abundance in this nephron segment. There was a concomitant increase of basolateral AE1 and α-cell number. Intercalated cell proliferation did not seem to play a role in the adaptation to acidosis. Alkali loading for 6-20 h after acidosis doubled the bicarbonate secretory flux and reduced proton secretion. Pendrin and AE1 expression patterns returned to control levels, demonstrating that adaptive changes by intercalated cells are rapidly reversible. Thus, regulation of intercalated cell anion exchanger expression and distribution plays a key role in adaptation of the cortical collecting duct to perturbations of acid/base.

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Year:  2010        PMID: 20592712      PMCID: PMC4487550          DOI: 10.1038/ki.2010.195

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  42 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-27       Impact factor: 11.205

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Authors:  T Matsumoto; G J Schwartz
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Authors:  S M Grassl; P S Aronson
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5.  Regulation of the expression of the Cl-/anion exchanger pendrin in mouse kidney by acid-base status.

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Journal:  Kidney Int       Date:  2002-12       Impact factor: 10.612

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Journal:  Pediatr Res       Date:  1996-01       Impact factor: 3.756

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Journal:  Am J Physiol       Date:  1985-08

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Authors:  L M Satlin; G J Schwartz
Journal:  J Cell Biol       Date:  1989-09       Impact factor: 10.539

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Review 3.  Collecting duct intercalated cell function and regulation.

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8.  Metabolic acidosis stimulates the production of the antimicrobial peptide cathelicidin in rabbit urine.

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9.  Insights into acidosis-induced regulation of SLC26A4 (pendrin) and SLC4A9 (AE4) transporters using three-dimensional morphometric analysis of β-intercalated cells.

Authors:  Jeffrey M Purkerson; Eric V Heintz; Aya Nakamori; George J Schwartz
Journal:  Am J Physiol Renal Physiol       Date:  2014-07-02

10.  Developmental loss, but not pharmacological suppression, of renal carbonic anhydrase 2 results in pyelonephritis susceptibility.

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