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Increased NBCn1 expression, Na(+)/ [Formula: see text] co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension
Genome-wide association studies have revealed an association between variation at the SLC4A7 locus and blood pressure. SLC4A7 encodes the electroneutral Na(+)/ [Formula: see text] co-transporter NBCn1 which regulates intracellular pH (pH(i)). We conducted a functional study of variants at this locus...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409084/ https://www.ncbi.nlm.nih.gov/pubmed/28087731 http://dx.doi.org/10.1093/hmg/ddx015 |
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author | Ng, Fu Liang Boedtkjer, Ebbe Witkowska, Kate Ren, Meixia Zhang, Ruoxin Tucker, Arthur Aalkjær, Christian Caulfield, Mark J. Ye, Shu |
author_facet | Ng, Fu Liang Boedtkjer, Ebbe Witkowska, Kate Ren, Meixia Zhang, Ruoxin Tucker, Arthur Aalkjær, Christian Caulfield, Mark J. Ye, Shu |
author_sort | Ng, Fu Liang |
collection | PubMed |
description | Genome-wide association studies have revealed an association between variation at the SLC4A7 locus and blood pressure. SLC4A7 encodes the electroneutral Na(+)/ [Formula: see text] co-transporter NBCn1 which regulates intracellular pH (pH(i)). 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 pH(i) 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 pH(i) 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. |
format | Online Article Text |
id | pubmed-5409084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54090842017-05-03 Increased NBCn1 expression, Na(+)/ [Formula: see text] co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension Ng, Fu Liang Boedtkjer, Ebbe Witkowska, Kate Ren, Meixia Zhang, Ruoxin Tucker, Arthur Aalkjær, Christian Caulfield, Mark J. Ye, Shu Hum Mol Genet Articles Genome-wide association studies have revealed an association between variation at the SLC4A7 locus and blood pressure. SLC4A7 encodes the electroneutral Na(+)/ [Formula: see text] co-transporter NBCn1 which regulates intracellular pH (pH(i)). 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 pH(i) 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 pH(i) 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. Oxford University Press 2017-03-01 2017-01-13 /pmc/articles/PMC5409084/ /pubmed/28087731 http://dx.doi.org/10.1093/hmg/ddx015 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ 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. |
spellingShingle | Articles Ng, Fu Liang Boedtkjer, Ebbe Witkowska, Kate Ren, Meixia Zhang, Ruoxin Tucker, Arthur Aalkjær, Christian Caulfield, Mark J. Ye, Shu Increased NBCn1 expression, Na(+)/ [Formula: see text] co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension |
title | Increased NBCn1 expression, Na(+)/ [Formula: see text] co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension |
title_full | Increased NBCn1 expression, Na(+)/ [Formula: see text] co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension |
title_fullStr | Increased NBCn1 expression, Na(+)/ [Formula: see text] co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension |
title_full_unstemmed | Increased NBCn1 expression, Na(+)/ [Formula: see text] co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension |
title_short | Increased NBCn1 expression, Na(+)/ [Formula: see text] co-transport and intracellular pH in human vascular smooth muscle cells with a risk allele for hypertension |
title_sort | increased nbcn1 expression, na(+)/ [formula: see text] co-transport and intracellular ph in human vascular smooth muscle cells with a risk allele for hypertension |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409084/ https://www.ncbi.nlm.nih.gov/pubmed/28087731 http://dx.doi.org/10.1093/hmg/ddx015 |
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