Lee Aven, Dawson Paul A, Markovich Daniel
School of Biomedical Sciences, University of Queensland, Brisbane, Qld 4072, Australia.
Int J Biochem Cell Biol. 2005 Jul;37(7):1350-6. doi: 10.1016/j.biocel.2005.02.013.
Sulfate (SO(4)2-) is an important anion regulating many metabolic and cellular processes. Maintenance of SO4(2-) homeostasis occurs in the renal proximal tubule via membrane transport proteins. Two SO(4)2- transporters that have been characterized and implicated in regulating serum SO4(2-) levels are: NaSi-1, a Na+-SO(4)2- cotransporter located at the brush border membrane and Sat-1, a SO4(2-)-anion exchanger located on the basolateral membranes of proximal tubular cells. Unlike Sat-1, for which very few studies have looked at regulation of its expression, NaSi-1 has been shown to be regulated by various hormones and dietary conditions in vivo. To study this further, NaSi-1 (SLC13A1) and Sat-1 (SLC26A1) gene structures were determined and recent studies have characterized their respective gene promoters. This review presents the current understanding of the transcriptional regulation of NaSi-1 and Sat-1, and describes possible pathogenetic implications which arise as a consequence of altered SO(4)2- homeostasis.
硫酸根离子(SO(4)2-)是一种重要的阴离子,参与调节许多代谢和细胞过程。肾近端小管通过膜转运蛋白维持SO4(2-)的内稳态。已被鉴定并与调节血清SO4(2-)水平相关的两种SO(4)2-转运蛋白分别是:NaSi-1,一种位于刷状缘膜的Na+-SO(4)2-协同转运蛋白;以及Sat-1,一种位于近端小管细胞基底外侧膜的SO4(2-)-阴离子交换蛋白。与Sat-1不同,对其表达调控的研究很少,而NaSi-1已被证明在体内受多种激素和饮食条件的调节。为进一步研究此问题,已确定了NaSi-1(SLC13A1)和Sat-1(SLC26A1)的基因结构,并且最近的研究对它们各自的基因启动子进行了表征。本综述介绍了目前对NaSi-1和Sat-1转录调控的理解,并描述了由于SO(4)2-内稳态改变而可能产生的致病影响。