Deaton J D, Guerrero T, Howard T H
Department of Pediatrics and Cell Biology and Anatomy, University of Alabama, School of Medicine, Birmingham.
Mol Biol Cell. 1992 Dec;3(12):1427-35. doi: 10.1091/mbc.3.12.1427.
In vitro Ca++ activates gelsolin to sever F-actin and form a gelsolin-actin (GA) complex at the+end of F-actin that is not dissociated by ethylene glycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid (EGTA) but is separated by EGTA+PIP/PIP2. The gelsolin blocks the+end on the actin filament, but the-end of the filament can still initiate actin polymerization. In thrombin activated platelets, evidence suggests that severing of F-actin by gelsolin increases GA complex, creates one-end actin nucleus and one cryptic+end actin nucleus per cut, and then dissociates to yield free+ends to nucleate rapid actin assembly. We examined the role of F-actin severing in creation and regulation of nuclei and polymerization in polymorphonuclear neutrophils (PMNs). At 2-s intervals after formyl peptide (FMLP) activation of endotoxin free (ETF) PMNs, change in GA complex was correlated with change in+end actin nuclei,-end actin nuclei, and F-actin content. GA complex was quantitated by electrophoretograms of proteins absorbed by antigelsolin from cells lysed in 10 mM EGTA,+end actin nuclei as cytochalasin (CD) sensitive and-end actin nuclei as CD insensitive increases in G-pyrenyl actin polymerization rates induced by the same PMNs, and F-actin content by NBDphallacidin binding to fixed cells. Thirty three percent of gelsolin was in GA complex in basal ETF PMNs; from 2-6 s, GA complexes dissociate (low = 15% at 10 s) and sequentially+end nuclei and F-actin content and then-end nuclei increase to a maximum at 10 s. At > s GA complex increase toward basal and + end nuclei and F-actin content returned toward basal. These kinetic data show gelsolin regulates availability of + end nuclei and actin polymerization in FMLP. However, absence of an initial increase in GA complex or - end nucleating activity shows FMLP activation does not cause gelsolin to sever F- or to bind G-actin to create cryptic + end nuclei in PMNs; the results suggest the + nucleus formation is gelsolin independent.
在体外,钙离子激活凝溶胶蛋白,使其切断F-肌动蛋白,并在F-肌动蛋白的正端形成凝溶胶蛋白-肌动蛋白(GA)复合物,该复合物不会被乙二醇双(β-氨基乙醚)-N,N,N',N'-四乙酸(EGTA)解离,但可被EGTA+磷脂酰肌醇/磷脂酰肌醇4,5-二磷酸(PIP/PIP2)分开。凝溶胶蛋白会封闭肌动蛋白丝上的正端,但丝的负端仍可引发肌动蛋白聚合。在凝血酶激活的血小板中,有证据表明凝溶胶蛋白切断F-肌动蛋白会增加GA复合物的形成,每次切断会产生一个单端肌动蛋白核和一个隐蔽的正端肌动蛋白核,然后解离产生游离的正端以启动快速的肌动蛋白组装。我们研究了F-肌动蛋白切断在多形核中性粒细胞(PMN)中核的形成、调控及聚合过程中的作用。在内毒素-free(ETF)PMN被甲酰肽(FMLP)激活后,每隔2秒,GA复合物的变化与正端肌动蛋白核、负端肌动蛋白核及F-肌动蛋白含量的变化相关。GA复合物通过用抗凝溶胶蛋白从在10 mM EGTA中裂解的细胞中吸收的蛋白质的电泳图谱进行定量,正端肌动蛋白核以细胞松弛素(CD)敏感,负端肌动蛋白核以CD不敏感来表示,由相同的PMN诱导的G-芘基肌动蛋白聚合速率增加,F-肌动蛋白含量通过NBD鬼笔环肽与固定细胞的结合来测定。在基础ETF PMN中,33%的凝溶胶蛋白处于GA复合物中;从2到6秒,GA复合物解离(在10秒时低至15%),随后正端核和F-肌动蛋白含量依次增加,然后负端核在10秒时增加到最大值。在>秒时,GA复合物向基础水平增加,正端核和F-肌动蛋白含量恢复到基础水平。这些动力学数据表明凝溶胶蛋白在FMLP中调节正端核的可用性和肌动蛋白聚合。然而,GA复合物或负端成核活性没有初始增加表明FMLP激活不会导致凝溶胶蛋白切断F-肌动蛋白或结合G-肌动蛋白以在PMN中产生隐蔽的正端核;结果表明正核的形成与凝溶胶蛋白无关。