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培养的PC12细胞在体积调节过程中的细胞骨架与离子运动

Cytoskeleton and ion movements during volume regulation in cultured PC12 cells.

作者信息

Cornet M, Ubl J, Kolb H A

机构信息

Laboratory of Cell and Tissue Biology, University of Liège, Belgium.

出版信息

J Membr Biol. 1993 Apr;133(2):161-70. doi: 10.1007/BF00233796.

Abstract

The present study investigates the role of cytoskeletal elements, microtubules and microfilaments, on ion transport systems activated during volume regulatory processes in PC12 pheochromocytoma cells. Disruption of microtubule network by colchicine (0.1 mM) or vinblastine sulfate (10 microM) has no significant effect on PC12 cell hydration or on changes of the intracellular K+, Cl- and Na+ content observed in hypo-osmotic conditions. Disruption of microfilament network by cytochalasin B strongly affects volume regulation in a dose-dependent manner. Cytochalasin B leads to a potentiation of the initial cell swelling and the regulatory volume decrease is suppressed. Although, the internal K+ and Cl- level decreases significantly, as demonstrated by measurements of intracellular ion content and 86Rb fluxes. Using the patch-clamp technique, we could demonstrate in PC12 cell membranes an ion channel whose gating is affected by application of a negative hydrostatic pressure (mechanical stress) to the membrane patch, by exposure of the cell to hypoosmotic medium (osmotic stress), or by disruption of the microfilament network with cytochalasin B.

摘要

本研究探讨细胞骨架成分,即微管和微丝,在PC12嗜铬细胞瘤细胞容积调节过程中激活的离子转运系统上所起的作用。用秋水仙碱(0.1 mM)或硫酸长春碱(10 microM)破坏微管网络,对PC12细胞的水合作用或在低渗条件下观察到的细胞内钾、氯和钠含量的变化没有显著影响。用细胞松弛素B破坏微丝网络以剂量依赖方式强烈影响容积调节。细胞松弛素B导致初始细胞肿胀增强,调节性容积减小受到抑制。尽管通过细胞内离子含量测量和86Rb通量证明,细胞内钾和氯水平显著降低。使用膜片钳技术,我们可以在PC12细胞膜中证明一种离子通道,其门控受以下因素影响:对膜片施加负静水压力(机械应力)、使细胞暴露于低渗介质(渗透应力)或用细胞松弛素B破坏微丝网络。

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