Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/39173
Title: Increased NBCn1 expression, Na+/HCO3- co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension.
Authors: Liang Ng, F.
Boedtkjer, E.
Witkowska, K.
Ren, M.
Zhang, R.
Tucker, A.
Aalkjær, C.
Caulfield, M. J.
Ye, Shu
First Published: 13-Jan-2017
Publisher: Oxford University Press (OUP)
Citation: Human Molecular Genetics, 2017
Abstract: Genome-wide association studies have revealed an association between variation at the SLC4A7 locus and blood pressure. SLC4A7 encodes the electroneutral Na(+)/HCO3 co-transporter NBCn1 which regulates intracellular pH (pHi). We conducted a functional study of variants at this locus in primary cultures of vascular smooth muscle and endothelial cells. In both cell types, we found genotype-dependent differences for rs13082711 in DNA-nuclear protein interactions, where the risk allele is associated with increased SLC4A7 expression level, NBCn1 availability and function as reflected in elevated steady-state pHi and accelerated recovery from intracellular acidosis. However, in the presence of Na(+)/H(+) exchange activity, the SLC4A7 genotypic effect on net base uptake and steady-state pHi persisted only in vascular smooth muscle cells but not endothelial cells. We found no discernable effect of the missense polymorphism resulting in the amino acid substitution Glu326Lys. The finding of a genotypic influence on SLC4A7 expression and pH i regulation in vascular smooth muscle cells provides an insight into the molecular mechanism underlying the association of variation at the SLC4A7 locus with blood pressure.
DOI Link: 10.1093/hmg/ddx015
ISSN: 0964-6906
eISSN: 1460-2083
Links: http://hmg.oxfordjournals.org/content/early/2017/01/13/hmg.ddx015
http://hdl.handle.net/2381/39173
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: © The Author 2017. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Appears in Collections:Published Articles, Dept. of Cardiovascular Sciences

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