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细胞体积的生物学意义。

The biological significance of cell volume.

作者信息

Lang F, Ritter M, Völkl H, Häussinger D

机构信息

Institute for Physiology, University of Innsbruck, Austria.

出版信息

Ren Physiol Biochem. 1993 Jan-Apr;16(1-2):48-65. doi: 10.1159/000173751.

Abstract

To survive, cells have to avoid excessive alterations of their volume. To this end, cells have developed a complex machinery of cell volume regulatory mechanisms comprising transport across the cell membrane and metabolism. Upon cell swelling, they loose electrolytes mainly via selective K+ channels and unselective ion channels and/or KCl symport, upon cell shrinkage they accumulate ions by Na+,K+,2Cl- cotransport and parallel operation of Na+/H+ exchange and Cl-/HCO3- exchange. In addition, cell shrinkage stimulates glycogenolysis, proteolysis and formation of organic osmolytes such as amino acids, methylamines and polyols. Cell swelling stimulates formation of glycogen and proteins and cellular release of organic osmolytes. Alterations of cell volume do play a crucial role in the regulation of cell function, as illustrated by four examples: 1. Epithelial transport may lead to cell swelling, which then triggers volume regulatory mechanisms modifying transcellular transport. 2. Insulin swells hepatocytes by activation of Na+,K+,2Cl- cotransport and Na+/H+ exchange, glucagon shrinks those cells by activation of ion channels. The respective volume changes participate in the regulation of cellular protein and glycogen metabolism by these hormones. 3. Growth factors and expression of ras oncogene activate Na+,K+,2Cl- cotransport and Na+/H+ exchange, leading to the respective cell swelling. 4. Hepatocyte swelling triggers a hepatorenal reflex decreasing renal blood flow.

摘要

为了生存,细胞必须避免其体积发生过度改变。为此,细胞已发展出一套复杂的细胞体积调节机制,包括跨细胞膜运输和代谢。细胞肿胀时,它们主要通过选择性钾离子通道、非选择性离子通道和/或氯化钾同向转运体来丢失电解质;细胞收缩时,它们通过钠钾氯共转运体以及钠氢交换体和氯碳酸氢根交换体的协同作用来积累离子。此外,细胞收缩会刺激糖原分解、蛋白质分解以及有机渗透溶质(如氨基酸、甲胺和多元醇)的形成。细胞肿胀则会刺激糖原和蛋白质的形成以及有机渗透溶质的细胞释放。细胞体积的改变在细胞功能调节中起着至关重要的作用,以下四个例子说明了这一点:1. 上皮运输可能导致细胞肿胀,进而触发调节机制改变跨细胞运输。2. 胰岛素通过激活钠钾氯共转运体和钠氢交换体使肝细胞肿胀,胰高血糖素通过激活离子通道使这些细胞收缩。相应的体积变化参与了这些激素对细胞蛋白质和糖原代谢的调节。3. 生长因子和ras癌基因的表达激活钠钾氯共转运体和钠氢交换体,导致相应的细胞肿胀。4. 肝细胞肿胀会引发肝肾反射,减少肾血流量。

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