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在培养的人上皮细胞的调节性容积减小过程中,胞质游离Ca2+的双相升高与K+和Cl-电导的激活相关。

Biphasic rises in cytosolic free Ca2+ in association with activation of K+ and Cl- conductance during the regulatory volume decrease in cultured human epithelial cells.

作者信息

Hazama A, Okada Y

机构信息

Department of Physiology, Kyoto University, Faculty of Medicine, Japan.

出版信息

Pflugers Arch. 1990 Aug;416(6):710-4. doi: 10.1007/BF00370619.

Abstract

During exposure to a hypotonic solution (55% osmolarity), cultured human epithelial (Intestine 407) cells exhibit a regulatory volume decrease after osmotic swelling. This process is known to involve parallel activation of volume-regulatory K+ and Cl- conductances. Biphasic increase in the cytosolic free Ca2+ concentration ([Ca2+]i) were observed by microspectrofluorometry, in fura-2-loaded cells upon hypotonic stress. Electrophysiological studies with Ca2(+)-selective and conventional microelectrodes indicated that a biphasic [Ca2+]i increase was associated with a biphasic hyperpolarization, whereas an interposing [Ca2+]i decrease coincided with a transient depolarization. A Ca2+ ionophore, ionomycin, produced a sustained Ca2+ increase and a prolonged hyperpolarization which was sensitive to the K+ channel blocker, quinine. A subsequent hypotonic challenge gave rise to a depolarization, which was sensitive to a stilbene-derivative Cl- channel blocker, without inducing further changes in [Ca2+]i. Normal cell volume regulation in a hypo-osmotic medium could take place even in the presence of ionomycin. It is concluded that a biphasic [Ca2+]i increase is closely associated with activation of the volume-regulatory K+ conductance, and that the interposing [Ca2+]i decrease is neither a causative factor for activation of the volume-regulatory Cl- conductance nor a prerequisite for regulatory volume decrease in epithelial cells exposed to a hypotonic solution.

摘要

在暴露于低渗溶液(渗透压为55%)期间,培养的人上皮(肠407)细胞在渗透性肿胀后会出现调节性容积减小。已知这一过程涉及容积调节性钾离子和氯离子通道的平行激活。通过显微荧光分光光度法,在低渗应激下对负载fura-2的细胞进行观察,发现胞质游离钙离子浓度([Ca2+]i)呈双相增加。使用钙离子选择性微电极和传统微电极进行的电生理研究表明,[Ca2+]i的双相增加与双相超极化相关,而其间的[Ca2+]i降低与短暂去极化同时发生。钙离子载体离子霉素可引起钙离子持续增加和超极化延长,这种超极化对钾离子通道阻滞剂奎宁敏感。随后的低渗刺激会导致去极化,该去极化对一种芪衍生物氯离子通道阻滞剂敏感,且不会引起[Ca2+]i的进一步变化。即使存在离子霉素,在低渗介质中正常的细胞容积调节仍可发生。得出的结论是,[Ca2+]i的双相增加与容积调节性钾离子通道的激活密切相关,且其间的[Ca2+]i降低既不是容积调节性氯离子通道激活的原因,也不是暴露于低渗溶液的上皮细胞调节性容积减小的先决条件。

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