Literature DB >> 29631353

Expression of the B splice variant of NBCe1 (SLC4A4) in the mouse kidney.

Lijuan Fang1, Hyun-Wook Lee1, Chao Chen1, Autumn N Harris1, Michael F Romero2, Jill W Verlander1, I David Weiner1,3.   

Abstract

Sodium-coupled bicarbonate transporters are critical for renal electrolyte transport. The electrogenic, sodium-coupled bicarbonate cotransporter, isoform 1 (NBCe1), encoded by the SLC4A4 geneencoded by the SLC4A4 gene has five multiple splice variants; the A splice variant, NBCe1-A, is the primary basolateral bicarbonate transporter in the proximal convoluted tubule. This study's purpose was to determine if there is expression of additional NBCe1 splice variants in the mouse kidney, their cellular distribution, and their regulation by metabolic acidosis. In wild-type mice, an antibody reactive only to NBCe1-A showed basolateral immunolabel only in cortical proximal tubule (PT) segments, whereas an antibody reactive to all NBCe1 splice variants (pan-NBCe1) showed basolateral immunolabel in PT segments in both the cortex and outer medulla. In mice with NBCe1-A deletion, the pan-NBCe1 antibody showed basolateral PT immunolabel in both the renal cortex and outer stripe of the outer medulla, and immunoblot analysis showed expression of a ~121-kDa protein. RT-PCR of mRNA from NBCe1-A knockout mice directed at splice variant-specific regions showed expression of only NBCe1-B mRNA. In wild-type kidney, RT-PCR confirmed expression of mRNA for the NBCe1-B splice variant and absence of mRNA for the C, D, and E splice variants. Finally, exogenous acid loading increased expression in the proximal straight tubule in the outer stripe of the outer medulla. These studies demonstrate that the NBCe1-B splice variant is present in the PT, and its expression increases in response to exogenous acid loading, suggesting it participates in the PT contribution to acid-base homeostasis.

Entities:  

Keywords:  SLC4A4; acidosis; bicarbonate; proximal tubule; transport

Mesh:

Substances:

Year:  2018        PMID: 29631353      PMCID: PMC6172571          DOI: 10.1152/ajprenal.00515.2017

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


  62 in total

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Journal:  Curr Opin Nephrol Hypertens       Date:  2013-09       Impact factor: 2.894

Review 4.  Metabolic Acidosis of CKD: An Update.

Authors:  Jeffrey A Kraut; Nicolaos E Madias
Journal:  Am J Kidney Dis       Date:  2015-10-23       Impact factor: 8.860

5.  Colonic anion secretory defects and metabolic acidosis in mice lacking the NBC1 Na+/HCO3- cotransporter.

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6.  Parallel adaptation of the rabbit renal cortical sodium/proton antiporter and sodium/bicarbonate cotransporter in metabolic acidosis and alkalosis.

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Review 7.  Modular structure of sodium-coupled bicarbonate transporters.

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8.  Collecting duct-specific Rh C glycoprotein deletion alters basal and acidosis-stimulated renal ammonia excretion.

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9.  Proximal tubule-specific glutamine synthetase deletion alters basal and acidosis-stimulated ammonia metabolism.

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Journal:  BMC Nephrol       Date:  2014-04-03       Impact factor: 2.388

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  8 in total

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2.  NBCe1-A is required for the renal ammonia and K+ response to hypokalemia.

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3.  Extrarenal Signs of Proximal Renal Tubular Acidosis Persist in Nonacidemic Nbce1b/c-Null Mice.

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4.  Differences in acidosis-stimulated renal ammonia metabolism in the male and female kidney.

Authors:  Autumn N Harris; Hyun-Wook Lee; Lijuan Fang; Jill W Verlander; I David Weiner
Journal:  Am J Physiol Renal Physiol       Date:  2019-08-07

5.  Acid-base effects of combined renal deletion of NBCe1-A and NBCe1-B.

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6.  Role of the renal androgen receptor in sex differences in ammonia metabolism.

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8.  Expression of the regulated isoform of the electrogenic Na+/HCO3- cotransporter, NBCe1, is enriched in pacemaker interstitial cells of Cajal.

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  8 in total

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