Literature DB >> 19129254

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

Hye-Young Kim1, Jill W Verlander, Jesse M Bishop, Brian D Cain, Ki-Hwan Han, Peter Igarashi, Hyun-Wook Lee, Mary E Handlogten, I David Weiner.   

Abstract

Ammonia metabolism and transport are critical for acid-base homeostasis. The ammonia transporter family member Rh C glycoprotein (Rhcg) is expressed in distal renal tubular segments, and its expression is regulated in parallel with renal ammonia metabolism. However, there are inconsistencies in its reported subcellular distribution, with both apical and basolateral Rhcg reported in rat and human kidney and only apical expression in mouse kidney. Because the membrane location of Rhcg is critical for understanding its physiological role, we reassessed mouse Rhcg localization using refined immunolocalization methods. Two antibodies directed against different Rhcg-specific epitopes identified both apical and basolateral Rhcg immunolabel in mouse kidney. Immunogold electron microscopy both confirmed basolateral plasma membrane Rhcg expression and showed that apical immunolabel represented expression in both the apical plasma membrane and in subapical cytoplasmic vesicles. Immunoblots and Northern blots identified similar bands in Balb/c and C57BL/6 kidneys, suggesting basolateral Rhcg may result from alternative trafficking. Basolateral Rhcg intensity was strain dependent, with less basolateral Rhcg expression in the Balb/c mouse compared with the C57BL/6 mouse. In mice with collecting duct-specific Rhcg gene deletion, generated using Cre-loxP techniques, neither apical nor basolateral Rhcg immunolabel was identified in the collecting duct, confirming that basolateral Rhcg was the product of the same gene product as apical Rhcg. Although basolateral Rhcg expression differed between C57BL/6 and Balb/c mice, Rh B glycoprotein, which is exclusively basolateral, was expressed at similar levels in the two strains. We conclude that Rhcg is present in both the apical and basolateral plasma membrane in the mouse kidney, where it is likely to contribute to renal ammonia metabolism.

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Year:  2009        PMID: 19129254      PMCID: PMC2660195          DOI: 10.1152/ajprenal.90637.2008

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


  46 in total

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Authors:  Ramanathan M Seshadri; Janet D Klein; Shelley Kozlowski; Jeff M Sands; Young-Hee Kim; Ki-Hwan Han; Mary E Handlogten; Jill W Verlander; I David Weiner
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8.  Identification of distinct subpopulations of intercalated cells in the mouse collecting duct.

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  40 in total

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Authors:  I David Weiner; Jill W Verlander
Journal:  Curr Opin Nephrol Hypertens       Date:  2010-09       Impact factor: 2.894

3.  NBCe1 expression is required for normal renal ammonia metabolism.

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4.  Effect of hypokalemia on renal expression of the ammonia transporter family members, Rh B Glycoprotein and Rh C Glycoprotein, in the rat kidney.

Authors:  Ki-Hwan Han; Hyun-Wook Lee; Mary E Handlogten; Jesse M Bishop; Moshe Levi; Jin Kim; Jill W Verlander; I David Weiner
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Review 5.  Role of NH3 and NH4+ transporters in renal acid-base transport.

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Review 6.  Ammonia Transporters and Their Role in Acid-Base Balance.

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Review 7.  Molecular mechanisms and regulation of urinary acidification.

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Journal:  Compr Physiol       Date:  2014-10       Impact factor: 9.090

Review 8.  Renal Tubular Acidosis: H+/Base and Ammonia Transport Abnormalities and Clinical Syndromes.

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Journal:  Adv Chronic Kidney Dis       Date:  2018-07       Impact factor: 3.620

9.  Expression of the ammonia transporter family member, Rh B Glycoprotein, in the human kidney.

Authors:  Ki-Hwan Han; Hyun-Wook Lee; Mary E Handlogten; Florence Whitehill; Gunars Osis; Byron P Croker; William L Clapp; Jill W Verlander; I David Weiner
Journal:  Am J Physiol Renal Physiol       Date:  2013-01-16

10.  Intercalated cell-specific Rh B glycoprotein deletion diminishes renal ammonia excretion response to hypokalemia.

Authors:  Jesse M Bishop; Hyun-Wook Lee; Mary E Handlogten; Ki-Hwan Han; Jill W Verlander; I David Weiner
Journal:  Am J Physiol Renal Physiol       Date:  2012-12-05
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