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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...

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Detalles Bibliográficos
Autores principales: Ng, Fu Liang, Boedtkjer, Ebbe, Witkowska, Kate, Ren, Meixia, Zhang, Ruoxin, Tucker, Arthur, Aalkjær, Christian, Caulfield, Mark J., Ye, Shu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
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
Descripción
Sumario: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.