Larsen E H, Ussing H H, Spring K R
Laboratory of Kidney and Electrolyte Metabolism, National Heart, Lung and Blood Institute, Bethesda, Maryland 20892.
J Membr Biol. 1987;99(1):25-40. doi: 10.1007/BF01870619.
The optical sectioning video imaging technique was used for measurements of the volume of mitochondria-rich (m.r.) cells of the isolated epithelium of toad skin. Under short-circuit conditions, cell volume decreased by about 14% in response to bilateral exposure to Cl-free (gluconate substitution) solutions, apical exposure to a sodium-free solution, or to amiloride. Serosal exposure to ouabain resulted in a large increase in volume, which could be prevented either by the simultaneous application of amiloride in the apical solution or by the exposure of the epithelium to bilateral Cl-free solutions. Unilateral exposure to a Cl-free solution did not prevent ouabain-induced cell swelling. It is concluded that m.r. cells have an amiloride-blockable Na conductance in the apical membrane, a ouabain-sensitive Na pump in the basolateral membrane, and a passive Cl permeability in both membranes. From the initial rate of ouabain-induced cell volume increase the active Na current carried by a single m.r. cell was estimated to be 9.9 +/- 1.3 pA. Voltage clamping of the preparation in the physiological range of potentials (0 to -100 mV, serosa grounded) resulted in a cell volume increase with a time course similar to that of the stimulation of the voltage-dependent Cl conductance. Volume increase and conductance activation were prevented by exposure of the tissue to a Cl-free apical solution. The steady-state volume of the m.r. cells increased with the clamping voltage, and at -100 mV the volume was about 1.15 times that under short-circuit conditions. The rate of volume increase during current passage was significantly decreased by lowering the serosal K concentration (Ki) to 0.5 mM, but was independent of whether Ki was 2.4, 5, or 10 mM. This indicates that the K conductance of the serosal membrane becomes rate limiting for the uptake of KCl when Ki is significantly lower than its physiological value. It is concluded that the voltage-activated Cl currents flow through the m.r. cells and that swelling is caused by an uptake of Cl ions from the apical bath and K ions from the serosal bath. Bilateral exposure of the tissue to hypo- or hypertonic bathing solutions changed cell volume without detectable changes in the Cl conductance. The volume response to external osmotic perturbations followed that of an osmometer with an osmotically inactive volume of 21%.(ABSTRACT TRUNCATED AT 400 WORDS)
光学切片视频成像技术用于测量蟾蜍皮肤分离上皮中富含线粒体(m.r.)细胞的体积。在短路条件下,双侧暴露于无氯(葡萄糖酸盐替代)溶液、顶端暴露于无钠溶液或阿米洛利后,细胞体积减少约14%。浆膜暴露于哇巴因导致体积大幅增加,这可通过在顶端溶液中同时应用阿米洛利或使上皮暴露于双侧无氯溶液来预防。单侧暴露于无氯溶液不能预防哇巴因诱导的细胞肿胀。结论是,m.r.细胞顶端膜具有阿米洛利可阻断的钠电导,基底外侧膜具有哇巴因敏感的钠泵,且两侧膜均具有被动氯通透性。根据哇巴因诱导的细胞体积增加的初始速率,估计单个m.r.细胞携带的主动钠电流为9.9±1.3 pA。在生理电位范围(0至 -100 mV,浆膜接地)对标本进行电压钳制导致细胞体积增加,其时间进程与电压依赖性氯电导刺激相似。组织暴露于无氯顶端溶液可防止体积增加和电导激活。m.r.细胞的稳态体积随钳制电压增加,在 -100 mV时体积约为短路条件下的1.15倍。将浆膜钾浓度(Ki)降至0.5 mM可显著降低电流通过期间的体积增加速率,但与Ki为2.4、5或10 mM无关。这表明当Ki显著低于其生理值时,浆膜的钾电导成为氯化钾摄取的速率限制因素。结论是,电压激活的氯电流流经m.r.细胞,肿胀是由从顶端浴摄取氯离子和从浆膜浴摄取钾离子引起的。组织双侧暴露于低渗或高渗浴液会改变细胞体积,但氯电导无明显变化。对外部渗透压扰动的体积反应遵循渗透计的反应,渗透惰性体积为21%。(摘要截短于400字)