Hall A C, Starks I, Shoults C L, Rashidbigi S
University Laboratory of Physiology, Oxford, United Kingdom.
Am J Physiol. 1996 May;270(5 Pt 1):C1300-10. doi: 10.1152/ajpcell.1996.270.5.C1300.
The contributions of various K+ transport pathways in bovine chondrocytes isolated from articular cartilage and their responses to changes in cell volume have been studied. K+(86Rb+) uptake mediated by the Na(+)-K(+) pump and Na(+)-K(+)-2Cl- cotransporter were stimulated by cell shrinkage, the latter as part of the regulatory volume increases (RVI) response, the former as an indirect effect resulting from the rise in intracellular Na+ concentration during RVI. For both transporters, there was an increase in the maximum velocity with no detectable effect on the Michaelis constant. There was no evidence for volume-sensitive K+ transport mediated by the K(+)-Cl- cotransporter, or Ca(2+)-activated K+ channels. However, chondrocyte swelling stimulated a ouabain- and bumetanide-insensitive K+ flux sensitive to pimozide and other drugs, which exhibited some of the properties of the relatively nonspecific volume-sensitive "osmolyte" channel described in other cell types.
对从关节软骨分离的牛软骨细胞中各种钾离子转运途径的作用及其对细胞体积变化的反应进行了研究。细胞收缩刺激了由钠钾泵和钠钾氯共转运体介导的钾离子(86铷离子)摄取,后者作为调节性容积增加(RVI)反应的一部分,前者是RVI期间细胞内钠离子浓度升高产生的间接效应。对于这两种转运体,最大速度均增加,而米氏常数未检测到变化。没有证据表明钾氯共转运体或钙激活钾通道介导容积敏感性钾离子转运。然而,软骨细胞肿胀刺激了对哇巴因和布美他尼不敏感、对匹莫齐特和其他药物敏感的钾离子通量,其表现出其他细胞类型中描述的相对非特异性容积敏感性“渗透溶质”通道的一些特性。