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麻醉剂激活磷脂酶C会降低细胞膜与细胞骨架的黏附力。

Phospholipase C activation by anesthetics decreases membrane-cytoskeleton adhesion.

作者信息

Raucher D, Sheetz M P

机构信息

Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

J Cell Sci. 2001 Oct;114(Pt 20):3759-66. doi: 10.1242/jcs.114.20.3759.

Abstract

Many different amphiphilic compounds cause an increase in the fluid-phase endocytosis rates of cells in parallel with a decrease in membrane-cytoskeleton adhesion. These compounds, however, do not share a common chemical structure, which leaves the mechanism and even site of action unknown. One possible mechanism of action is through an alteration of inositol lipid metabolism by modifying the cytoplasmic surface of the plasma membrane bilayer. By comparing permeable amphiphilic amines used as local anesthetics with their impermeable analogs, we find that access to the cytoplasmic surface is necessary to increase endocytosis rate and decrease membrane-cytoskeleton adhesion. In parallel, we find that the level of phosphatidylinositol 4,5-bisphosphate (PIP(2)) in the plasma membrane is decreased and cytoplasmic Ca(2+) is increased only by permeable amines. The time course of both the decrease in plasma membrane PIP(2) and the rise in Ca(2+) parallels the decrease in cytoskeleton-membrane adhesion. Inositol labeling shows that phosphatidylinositol-4-phosphate levels are increased by the permeable anesthetics, indicating that lipid turnover is increased. Consistent with previous observations, phospholipase C (PLC) inhibitors block anesthetic effects on the PIP(2) and cytoplasmic Ca(2+) levels, as well as the drop in adhesion. Therefore, we suggest that PLC activity is increased by amine anesthetics at the cytoplasmic surface of the plasma membrane, which results in a decrease in membrane-cytoskeleton adhesion.

摘要

许多不同的两亲性化合物会导致细胞液相内吞率增加,同时膜 - 细胞骨架黏附力下降。然而,这些化合物并不具有共同的化学结构,这使得作用机制甚至作用位点都尚不明确。一种可能的作用机制是通过修饰质膜双层的细胞质表面来改变肌醇脂质代谢。通过比较用作局部麻醉剂的可渗透两亲性胺与其不可渗透的类似物,我们发现进入细胞质表面对于提高内吞率和降低膜 - 细胞骨架黏附力是必要的。同时,我们发现只有可渗透胺会使质膜中磷脂酰肌醇4,5 - 二磷酸(PIP₂)水平降低,细胞质Ca²⁺增加。质膜PIP₂降低和Ca²⁺升高的时间进程与细胞骨架 - 膜黏附力的降低相平行。肌醇标记显示,可渗透麻醉剂会使磷脂酰肌醇 - 4 - 磷酸水平升高,表明脂质周转率增加。与先前的观察结果一致,磷脂酶C(PLC)抑制剂可阻断麻醉剂对PIP₂和细胞质Ca²⁺水平的影响,以及黏附力的下降。因此,我们认为胺类麻醉剂在质膜的细胞质表面会增加PLC活性,从而导致膜 - 细胞骨架黏附力下降。

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