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SLC20蛋白家族:兼具钠磷共转运体和病毒受体的双重功能。

The SLC20 family of proteins: dual functions as sodium-phosphate cotransporters and viral receptors.

作者信息

Collins James F, Bai Liqun, Ghishan Fayez K

机构信息

Department of Pediatrics, Steele Memorial Children's Research Center, University of Arizona College of Medicine, 1501 N. Campbell Ave., P.O. Box 245073, Tucson, AZ 85724, USA.

出版信息

Pflugers Arch. 2004 Feb;447(5):647-52. doi: 10.1007/s00424-003-1088-x. Epub 2003 May 21.

DOI:10.1007/s00424-003-1088-x
PMID:12759754
Abstract

The SLC20 family transport proteins were originally identified as retroviral receptors (called Glvr-1 and Ram-1). Since then, they have been shown to function as sodium-phosphate (Na/P(i)) cotransporters, and have subsequently been classified as type III Na/P(i) cotransporters (now called Pit-1 and Pit-2). The Pit cotransporters share approximately 60% sequence homology, they have a high affinity for P(i), they are electrogenic with a coupling stoichiometry of >1 Na(+) per P(i) ion cotransported, and are inhibited by alkaline pH and phosphonoformic acid (PFA). Pit-1 and Pit-2 expression and/or activity has also been shown to be regulated by P(i) deprivation in some, but not all cells and tissues examined. The Pit-1 and Pit-2 cotransporters are widely expressed, but cell-type specific expression has only been investigated in bone, kidney and intestine. Both proteins are likely expressed on the basolateral membranes of polarized epithelial cells, where they are likely involved in cellular P(i) homeostasis. The Pit-1 and Pit-2 gene promoters have been cloned and characterized. While the exact roles of the Pit cotransporters in different cell types has not been definitively determined, they may be involved in important physiological pathways in bone, aortic smooth muscle cells, parathyroid glands, kidney and intestine.

摘要

溶质载体家族20(SLC20)转运蛋白最初被鉴定为逆转录病毒受体(称为Glvr-1和Ram-1)。从那时起,它们已被证明具有钠-磷酸盐(Na/P(i))共转运体的功能,随后被归类为III型Na/P(i)共转运体(现在称为Pit-1和Pit-2)。Pit共转运体具有约60%的序列同源性,它们对P(i)具有高亲和力,它们是电生性的,每共转运1个P(i)离子的偶联化学计量>1个Na(+),并且受到碱性pH和膦甲酸(PFA)的抑制。在一些但并非所有检测的细胞和组织中,Pit-1和Pit-2的表达和/或活性也已被证明受P(i)缺乏的调节。Pit-1和Pit-2共转运体广泛表达,但仅在骨、肾和肠道中研究了细胞类型特异性表达。这两种蛋白可能都表达于极化上皮细胞的基底外侧膜上,在那里它们可能参与细胞内P(i)的稳态。Pit-1和Pit-2基因启动子已被克隆和表征。虽然Pit共转运体在不同细胞类型中的确切作用尚未明确确定,但它们可能参与骨、主动脉平滑肌细胞、甲状旁腺、肾和肠道中的重要生理途径。

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