Hibbert Julie E, Butt R Hussain, Coorssen Jens R
Department of Physiology and Biophysics, Faculty of Medicine, University of Calgary, Calgary, Alta., Canada T2N 4N1.
Int J Biochem Cell Biol. 2006 Mar;38(3):461-71. doi: 10.1016/j.biocel.2005.10.008. Epub 2005 Nov 8.
Actin has been suggested as an essential component in the membrane fusion stage of exocytosis. In some model systems disruption of the actin filament network associated with exocytotic membranes results in a decrease in secretion. Here we analyze the fast Ca2+-triggered membrane fusion steps of regulated exocytosis using a stage-specific preparation of native secretory vesicles (SV) to directly test whether actin plays an essential role in this mechanism. Although present on secretory vesicles, selective pharmacological inhibition of actin did not affect the Ca2+-sensitivity, extent, or kinetics of membrane fusion, nor did the addition of exogenous actin or an anti-actin antibody. There was also no discernable affect on inter-vesicle contact (docking). Overall, the results do not support a direct role for actin in the fast, Ca2+-triggered steps of regulated membrane fusion. It would appear that actin acts elsewhere within the exocytotic cycle.
肌动蛋白被认为是胞吐作用膜融合阶段的一个重要组成部分。在一些模型系统中,与胞吐膜相关的肌动蛋白丝网络的破坏会导致分泌减少。在这里,我们使用天然分泌囊泡(SV)的阶段特异性制剂来分析调节性胞吐作用中快速Ca2+触发的膜融合步骤,以直接测试肌动蛋白在这一机制中是否发挥重要作用。尽管肌动蛋白存在于分泌囊泡上,但对肌动蛋白的选择性药理抑制并不影响膜融合的Ca2+敏感性、程度或动力学,添加外源肌动蛋白或抗肌动蛋白抗体也没有影响。对囊泡间接触(对接)也没有明显影响。总体而言,这些结果不支持肌动蛋白在快速、Ca2+触发的调节性膜融合步骤中起直接作用。看来肌动蛋白在胞吐循环的其他地方起作用。