Dong J, Delamere N A
Department of Ophthalmology and Visual Science, Kentucky Lions Eye Research Institute, Louisville.
Am J Physiol. 1994 Dec;267(6 Pt 1):C1553-60. doi: 10.1152/ajpcell.1994.267.6.C1553.
We examined the regulation of Na(+)-K(+)-2Cl- transporter activity by protein kinase C (PKC) in a cell line derived from rabbit nonpigmented ciliary epithelium. Na(+)-K(+)-2Cl- cotransporter activity was measured as the rate of bumetanide-sensitive potassium (86Rb) transport. Phorbol 12,13-dibutyrate (PBDu) was used to activate PKC. PBDu inhibited bumetanide-sensitive potassium (86Rb) uptake, with a half-maximal inhibitory concentration of approximately 0.1 microM. The inhibitory effect of PBDu on potassium uptake by the N(+)-K(+)-2Cl- cotransporter was abolished by PCK downregulation and diminished by 1-(5-isoquinolinylsulfonyl)-2-methylpiperazine, a PKC inhibitor. PBDu inhibited Na(+)-K(+)-2Cl- cotransporter-mediated inward potassium (86Rb) transport by approximately 26% in control cells and by 40% in cells pretreated with ouabain. PKC activation also reduced the rate of bumetanide-sensitive potassium (86Rb) efflux in ouabain-treated cells but not in control (no oubain) cells. PBDu caused little change of intracellular sodium, potassium, or chloride, suggesting that an alteration of cytoplasmic ion composition is not responsible for the observed PBDu-induced changes in the rate of either inward or outward potassium movement mediated by the Na(+)-K(+)-2Cl- cotransporter.
我们在源自兔非色素睫状上皮的细胞系中研究了蛋白激酶C(PKC)对Na(+)-K(+)-2Cl-转运体活性的调节作用。Na(+)-K(+)-2Cl-协同转运体活性通过布美他尼敏感的钾(86Rb)转运速率来测定。佛波醇12,13-二丁酸酯(PBDu)用于激活PKC。PBDu抑制布美他尼敏感的钾(86Rb)摄取,半数最大抑制浓度约为0.1 microM。PKC下调可消除PBDu对N(+)-K(+)-2Cl-协同转运体钾摄取的抑制作用,而PKC抑制剂1-(5-异喹啉磺酰基)-2-甲基哌嗪可减弱该抑制作用。在对照细胞中,PBDu抑制Na(+)-K(+)-2Cl-协同转运体介导的内向钾(86Rb)转运约26%,在用哇巴因预处理的细胞中抑制约40%。PKC激活还降低了哇巴因处理细胞中布美他尼敏感的钾(86Rb)外流速率,但在对照(未用哇巴因)细胞中未降低。PBDu对细胞内钠、钾或氯的影响很小,这表明细胞质离子组成的改变并非PBDu诱导的由Na(+)-K(+)-2Cl-协同转运体介导的内向或外向钾转运速率变化的原因。