Du Juan, Fu Jie, Xia Xian-ming, Shen Bing
Department of Physiology, School of Basic Medicine, Anhui Medical University, Hefei 230032, China.
Department of Gastroenterology and Hepatology, The Fourth Affiliated Hospital of Anhui Medical University, Hefei 230032, China.
Acta Pharmacol Sin. 2016 Jan;37(1):13-8. doi: 10.1038/aps.2015.126.
TRPP2 (polycystin-2, PC2 or PKD2), encoded by the PKD2 gene, is a non-selective cation channel with a large single channel conductance and high Ca(2+) permeability. In cell membrane, TRPP2, along with polycystin-1, TRPV4 and TRPC1, functions as a mechanotransduction channel. In the endoplasmic reticulum, TRPP2 modulates intracellular Ca(2+) release associated with IP3 receptors and the ryanodine receptors. Noteworthily, TRPP2 is widely expressed in vascular endothelial and smooth muscle cells of all major vascular beds, and contributes to the regulation of vessel function. The mutation of the PKD2 gene is a major cause of autosomal dominant polycystic kidney disease (ADPKD), which is not only a common genetic disease of the kidney but also a systemic disorder associated with abnormalities in the vasculature; cardiovascular complications are the leading cause of mortality and morbidity in ADPKD patients. This review provides an overview of the current knowledge regarding the TRPP2 protein and its possible role in cardiovascular function and related diseases.
TRPP2(多囊蛋白-2、PC2或PKD2)由PKD2基因编码,是一种具有大单通道电导和高Ca(2+)通透性的非选择性阳离子通道。在细胞膜中,TRPP2与多囊蛋白-1、TRPV4和TRPC1一起作为机械转导通道发挥作用。在内质网中,TRPP2调节与IP3受体和兰尼碱受体相关的细胞内Ca(2+)释放。值得注意的是,TRPP2在所有主要血管床的血管内皮和平滑肌细胞中广泛表达,并有助于血管功能的调节。PKD2基因的突变是常染色体显性多囊肾病(ADPKD)的主要原因,ADPKD不仅是一种常见的肾脏遗传病,也是一种与血管系统异常相关的全身性疾病;心血管并发症是ADPKD患者死亡和发病的主要原因。本综述概述了目前关于TRPP2蛋白及其在心血管功能和相关疾病中可能作用的知识。