Literature DB >> 16896189

Cellular distribution of the potassium channel KCNQ1 in normal mouse kidney.

Wencui Zheng1, Jill W Verlander, I Jeanette Lynch, Melanie Cash, Jiahong Shao, Lisa R Stow, Brian D Cain, I David Weiner, Susan M Wall, Charles S Wingo.   

Abstract

Mechanisms of K(+) secretion and absorption along the collecting duct are not understood fully. Because KCNQ1 participates in K(+) secretion within the inner ear and stomach, distribution of KCNQ1 in mouse kidney was studied using Northern and Western analyses, RT-PCR of isolated tubules, and immunohistochemistry. Northern blots demonstrated KCNQ1 transcripts in whole kidney. RT-PCR showed KCNQ1 mRNA in isolated distal convoluted tubule (DCT), connecting segment (CNT), collecting ducts (CD), and glomeruli. Immunoblots of kidney and stomach revealed a approximately 75-kDa protein, the expected mobility for KCNQ1. KCNQ1 was detected by immunohistochemistry throughout the distal nephron and CD. Thick ascending limbs exhibited weak basolateral immunolabel. In DCT and CNT cells, immunolabel was intense and basolateral, although KCNQ1 label was stronger in late than in early DCT. Initial collecting tubule and cortical CD KCNQ1 immunolabel was predominantly diffuse, but many cells exhibited discrete apical label. Double-labeling experiments demonstrated that principal cells, type B intercalated cells, and a few type A intercalated cells exhibited distinct apical KCNQ1 immunolabel. In inner medullary CD, principal cells exhibited distinct basolateral KCNQ1 immunolabel, whereas intercalated cells showed diffuse cytoplasmic staining. Thus KCNQ1 protein is widely distributed in mouse distal nephron and CD, with significant axial and cellular heterogeneity in location and intensity. These findings suggest that KCNQ1 has cell-specific roles in renal ion transport and may participate in K(+) secretion and/or absorption along the thick ascending limb, DCT, connecting tubule, and CD.

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Year:  2006        PMID: 16896189     DOI: 10.1152/ajprenal.00087.2006

Source DB:  PubMed          Journal:  Am J Physiol Renal Physiol        ISSN: 1522-1466


  16 in total

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Authors:  Vidya K Nagalakshmi; Volkhard Lindner; Andy Wessels; Jing Yu
Journal:  Dev Dyn       Date:  2014-11-23       Impact factor: 3.780

Review 2.  Distal convoluted tubule.

Authors:  James A McCormick; David H Ellison
Journal:  Compr Physiol       Date:  2015-01       Impact factor: 9.090

Review 3.  Regulation of transport in the connecting tubule and cortical collecting duct.

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Review 4.  KCNE4 and KCNE5: K(+) channel regulation and cardiac arrhythmogenesis.

Authors:  Geoffrey W Abbott
Journal:  Gene       Date:  2016-07-30       Impact factor: 3.688

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Journal:  Am J Physiol Renal Physiol       Date:  2010-09-22

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Review 7.  Basolateral membrane K+ channels in renal epithelial cells.

Authors:  Kirk L Hamilton; Daniel C Devor
Journal:  Am J Physiol Renal Physiol       Date:  2012-02-15

8.  KCNQ1 and KCNE1 K+ channel components are involved in early left-right patterning in Xenopus laevis embryos.

Authors:  Junji Morokuma; Douglas Blackiston; Michael Levin
Journal:  Cell Physiol Biochem       Date:  2008-04-24

Review 9.  Thick Ascending Limb Sodium Transport in the Pathogenesis of Hypertension.

Authors:  Agustin Gonzalez-Vicente; Fara Saez; Casandra M Monzon; Jessica Asirwatham; Jeffrey L Garvin
Journal:  Physiol Rev       Date:  2019-01-01       Impact factor: 37.312

10.  Basolateral expression of the ammonia transporter family member Rh C glycoprotein in the mouse kidney.

Authors:  Hye-Young Kim; Jill W Verlander; Jesse M Bishop; Brian D Cain; Ki-Hwan Han; Peter Igarashi; Hyun-Wook Lee; Mary E Handlogten; I David Weiner
Journal:  Am J Physiol Renal Physiol       Date:  2009-01-07
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