多磷酸肌苷作为膜骨架稳定性的调节因子。

Kroc Foundation series Pub Date : 1984-01-01
M P Sheetz, W P Wang, D L Kreutzer
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引用次数: 0

摘要

膜骨架是肌动蛋白、谱蛋白和相关蛋白的二维复合体,位于大多数质膜的细胞质表面。该复合物的组分被认为控制整体膜蛋白的横向迁移以及影响细胞形状和运动。在早期的研究中,我们观察到添加多磷酸肌醇脂可以增加膜骨架的解离。在白细胞功能的初步研究中,我们观察到添加Trental后趋化性的增加与多磷酸肌醇水平的增加有关。因此,我们认为,多磷酸肌苷有助于,如果不是必需的,细胞的流动性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polyphosphoinositides as regulators of membrane skeletal stability.

The membrane skeleton is a two-dimensional complex of actin, spectrinlike, and associated proteins which lies on the cytoplasmic face of most plasma membranes. Components of this complex are believed to control the lateral mobility of integral membrane proteins as well as influence cell shape and motility. In earlier studies we observed that the addition of polyphosphorylated inositol lipids could increased membrane skeleton dissociation. In preliminary studies of leukocyte function we have observed that increased chemotaxis with Trental addition is correlated with increased polyphosphoinositide levels. Consequently, we suggest that polyphosphoinositides contribute to, if not are requisite for, cellular mobility.

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