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渗透收缩对Madin-Darby犬肾细胞离子电导的抑制作用。

Inhibition of ion conductances by osmotic shrinkage of Madin-Darby canine kidney cells.

作者信息

Ritter M, Steidl M, Lang F

机构信息

Institute for Physiology, University of Innsbruck, Austria.

出版信息

Am J Physiol. 1991 Oct;261(4 Pt 1):C602-7. doi: 10.1152/ajpcell.1991.261.4.C602.

Abstract

Osmotic swelling of Madin-Darby canine kidney (MDCK) cells enhances the ion conductances of the cell membrane, which allows release of cellular ions and subsequent regulatory cell volume decrease. The present study has been performed to test whether cell shrinkage similarly affects the ion conductances of MDCK cell membranes. Increase of extracellular osmolarity by addition of 50 mM NaCl or 100 mM mannitol leads within 3 min to a hyperpolarization of the cell membrane, a marked increase of cell membrane resistance [by 223 +/- 38% (n = 8) and 228 +/- 21% (n = 5), respectively], as well as a moderate increase of the K+ selectivity of the cell membrane (by 37 +/- 13%, n = 9). Thus exposure to hypertonic extracellular fluid decreases the cell membrane conductances including the K+ conductance. Cell volume measurements reveal a regulatory cell volume increase, which is sensitive to both furosemide and dimethylamiloride. Extracellular ATP (10 microM), which activates calcium-sensitive K+ channels, hyperpolarizes the cell membrane close to the K+ equilibrium potential. The respective values are -69.9 +/- 3.1 mV (n = 9) in isotonic fluid, -79.4 +/- 1.8 mV (n = 9) within 3 min, and -76.4 +/- 1.8 mV (n = 7) within 16-h exposure to hypertonic extracellular fluid. This observation points to a sustained increase of intracellular K+ activity after exposure to hypertonic extracellular fluid.

摘要

马-达二氏犬肾(MDCK)细胞的渗透性肿胀增强了细胞膜的离子电导,这使得细胞内离子释放并随后调节细胞体积减小。本研究旨在测试细胞收缩是否同样影响MDCK细胞膜的离子电导。通过添加50 mM NaCl或100 mM甘露醇使细胞外渗透压升高,在3分钟内导致细胞膜超极化、细胞膜电阻显著增加[分别增加223±38%(n = 8)和228±21%(n = 5)],以及细胞膜K+选择性适度增加(增加37±13%,n = 9)。因此,暴露于高渗细胞外液会降低包括K+电导在内的细胞膜电导。细胞体积测量显示细胞体积有调节性增加,这对呋塞米和二甲基氨氯吡脒均敏感。细胞外ATP(10 microM)可激活钙敏感性K+通道,使细胞膜超极化至接近K+平衡电位。在等渗液中的相应值为-69.9±3.1 mV(n = 9),在3分钟内为-79.4±1.8 mV(n = 9),在暴露于高渗细胞外液16小时内为-76.4±1.8 mV(n = 7)。这一观察结果表明,暴露于高渗细胞外液后细胞内K+活性持续增加。

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