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人类多形核白细胞中肌动蛋白聚合/解聚的振荡反应

Oscillating actin polymerization/depolymerization responses in human polymorphonuclear leukocytes.

作者信息

Omann G M, Porasik M M, Sklar L A

机构信息

Department of Surgery, University of Michigan Medical School, Ann Arbor 48109.

出版信息

J Biol Chem. 1989 Oct 5;264(28):16355-8.

PMID:2550438
Abstract

Leukotriene B4 and platelet-activating factor induced a rapidly oscillating actin polymerization/depolymerization response in human polymorphonuclear leukocytes. N-Formylpeptides were deficient in the ability to induce these oscillations. Flow cytometric analysis of filamentous actin verified that all cells were synchronously responding in this cyclic manner. The hypothesis was tested that these oscillations were analogous to chemical oscillations, i.e. oscillations of intermediate species in chemical systems that are far from equilibrium (Epstein, I. R., Kustin, K., DeKepper, P., and Orban, M. (1983) Sci. Am. 248, 112). Actin polymerization/depolymerization cycles were terminated by adding receptor antagonist a few seconds after initiation of the response by agonists. Thus the oscillations did not represent chemical oscillations that hypothetically could result from a rapid jump of the intracellular milieu to a state far from equilibrium. Rather, continued occupancy of receptors and/or occupancy of new receptors was required to sustain the oscillations. This suggested that the oscillations resulted from regulated polymerization and depolymerization pathways. In simultaneous measurements of actin-associated right angle light scatter and intracellular calcium, no calcium oscillations were detected. Thus, cycles of actin polymerization/depolymerization were not regulated by calcium oscillations.

摘要

白三烯B4和血小板活化因子可在人多形核白细胞中诱导快速振荡的肌动蛋白聚合/解聚反应。N-甲酰肽缺乏诱导这些振荡的能力。丝状肌动蛋白的流式细胞术分析证实,所有细胞均以这种循环方式同步反应。有人提出一个假设,即这些振荡类似于化学振荡,也就是远离平衡态的化学系统中中间物种的振荡(爱泼斯坦,I.R.,库斯汀,K.,德凯珀,P.,和奥尔班,M.(1983年)《科学美国人》248,112)。在激动剂引发反应几秒钟后加入受体拮抗剂,可终止肌动蛋白聚合/解聚循环。因此,这些振荡并不代表假设中可能由细胞内环境迅速跃迁至远离平衡态而产生的化学振荡。相反,需要持续占据受体和/或占据新的受体来维持振荡。这表明振荡是由受调控的聚合和解聚途径引起的。在同时测量与肌动蛋白相关的直角光散射和细胞内钙时,未检测到钙振荡。因此,肌动蛋白聚合/解聚循环不受钙振荡的调控。

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