Ng Fu Liang, Boedtkjer Ebbe, Witkowska Kate, Ren Meixia, Zhang Ruoxin, Tucker Arthur, Aalkjær Christian, Caulfield Mark J, Ye Shu
Department of Clinical Pharmacology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Hum Mol Genet. 2017 Mar 1;26(5):989-1002. doi: 10.1093/hmg/ddx015.
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 pHi 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.
全基因组关联研究揭示了SLC4A7基因座变异与血压之间的关联。SLC4A7编码电中性Na⁺/HCO₃⁻共转运蛋白NBCn1,该蛋白调节细胞内pH值(pHi)。我们对血管平滑肌和内皮细胞原代培养物中该基因座的变异进行了功能研究。在这两种细胞类型中,我们发现rs13082711在DNA-核蛋白相互作用中存在基因型依赖性差异,其中风险等位基因与SLC4A7表达水平升高、NBCn1可用性增加以及功能增强有关,这体现在稳态pHi升高和细胞内酸中毒恢复加速上。然而,在存在Na⁺/H⁺交换活性的情况下,SLC4A7基因型对净碱基摄取和稳态pHi的影响仅在血管平滑肌细胞中持续存在,而在内皮细胞中则不存在。我们没有发现导致氨基酸替换Glu326Lys的错义多态性有明显影响。血管平滑肌细胞中基因型对SLC4A7表达和pHi调节的影响这一发现,为深入了解SLC4A7基因座变异与血压关联的分子机制提供了线索。