Suzuki M
Department of Pharmacology, Jichi Medical School, Tochigi, Japan.
Nihon Jinzo Gakkai Shi. 1995 Aug;37(8):422-7.
The renal collecting tubules are responsible for secretion of K+ into the urine and play a major regulatory role in K+ homeostasis of mammals. There are several factors which affect K+ secretion, including aldosterone, K intakes and acid-base balance. We have cloned a complementary DNA encoding a K+ channel of the rabbit renal cortical collecting tubule cells (RACTK1). RACTK1 is a voltage-independent, pH sensitive K(+)-permeable channel, encoding 284 amino-acids, and putatively having two transmembrane segments. This channel is located not only in the luminal membrane of the collecting duct but also in the vascular smooth muscles of the several arteries. The expression of RACTK1 is regulated by external pH but neither by aldosterone nor by K+ concentration in cultured cells. Thus RACTK1 seems to be a unique and distinct from K+ channels in that it is regulated specifically by changes in ambient pH, contributing to the pH dependent urinary K+ excretion.
肾集合小管负责将K⁺分泌到尿液中,并在哺乳动物的K⁺稳态中发挥主要调节作用。有几个因素会影响K⁺分泌,包括醛固酮、K⁺摄入量和酸碱平衡。我们克隆了一个编码兔肾皮质集合小管细胞K⁺通道(RACTK1)的互补DNA。RACTK1是一种电压非依赖性、pH敏感的K⁺通透通道,编码284个氨基酸,推测有两个跨膜片段。该通道不仅位于集合管的管腔膜中,还位于几条动脉的血管平滑肌中。RACTK1的表达受细胞外pH调节,但不受醛固酮或培养细胞中K⁺浓度的调节。因此,RACTK1似乎是一种独特的K⁺通道,因为它受环境pH变化的特异性调节,有助于pH依赖性尿K⁺排泄。