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Ouabain-Induced Cytoplasmic Vesicles and Their Role in Cell Volume Maintenance

机译:Ouabain诱导的细胞质囊泡及其在细胞体积维持中的作用

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摘要

Cellular swelling is controlled by an active mechanism of cell volume regulation driven by a Na+/K+-dependent ATPase and by aquaporins which translocate water along the osmotic gradient. Na+/K+-pump may be blocked by ouabain, a digitalic derivative, by inhibition of ATP, or by drastic ion alterations of extracellular fluid. However, it has been observed that some tissues are still able to control their volume despite the presence of ouabain, suggesting the existence of other mechanisms of cell volume control. In 1977, by correlating electron microscopy observation with ion and water composition of liver slices incubated in different metabolic conditions in the presence or absence of ouabain, we observed that hepatocytes were able to control their volume extruding water and recovering ion composition in the presence of ouabain. In particular, hepatocytes were able to sequester ions and water in intracellular vesicles and then secrete them at the bile canaliculus pole. We named this “vesicular mechanism of cell volume control.” Afterward, this mechanism has been confirmed by us and other laboratories in several mammalian tissues. This review summarizes evidences regarding this mechanism, problems that are still pending, and questions that need to be answered. Finally, we shortly review the importance of cell volume control in some human pathological conditions.
机译:通过由Na + / K + +依赖性ATP酶和沿渗透梯度汇编水的水通道蛋白的电池体积调节的活性机制来控制细胞溶胀。 Na + / k + -pump可以被Ouabain,赋形剂,通过抑制ATP或细胞外液的激烈改变来阻塞。然而,已经观察到,尽管存在Ouabain,一些组织仍然能够控制其体积,这表明存在细胞体积控制的其他机制。 1977年,通过将电子显微镜观察与肝脏不同代谢条件的离子和水组合物相关,我们观察到肝细胞能够在奥巴班存在下控制其体积挤出水和回收离子组合物。特别地,肝细胞能够在细胞内囊泡中螯合离子和水,然后在胆汁穴位杆处分泌它们。我们将此命名为此“细胞体积控制的凹凸机制”。之后,这种机制已被美国和其他几个哺乳动物组织中的实验室确认。本综述总结了有关此机制的证据,仍处于未决的问题以及需要回答的问题。最后,我们不久审查了细胞体积控制在某些人类病理条件下的重要性。

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