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过氧化氢诱导的细胞F-肌动蛋白增加并未伴随着肌动蛋白成核活性的增加。

H2O2-induced increases in cellular F-actin occur without increases in actin nucleation activity.

作者信息

Omann G M, Harter J M, Burger J M, Hinshaw D B

机构信息

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

出版信息

Arch Biochem Biophys. 1994 Feb 1;308(2):407-12. doi: 10.1006/abbi.1994.1057.

Abstract

Previous work has shown that H2O2 causes an increase in polymerized actin (F-actin) inside cells. To test the hypothesis that increased polymerization resulted from a mechanism involving increased actin nucleation activity, we employed methods utilizing pyrene-labeled actin to quantify the actin nucleation activity of cell lysates and N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) (NBD)-phallacidin binding assays to quantify the amount of F-actin in P388D1 cells. H2O2 increased polymerized actin (NBD-phallacidin assay) in a dose-dependent manner with an effective dose giving 50% response (ED50) approximately 1 mM. Five millimolar H2O2 caused a 1.6-fold increase in NBD-phallacidin staining. In contrast, actin nucleation activity decreased in a dose-dependent manner with a similar ED50. Five millimolar H2O2 caused a 30-40% decrease in actin nucleation activity. The effect was rapid, occurring within 5 min of H2O2 addition. The results indicate that H2O2 causes cytoskeletal changes that enhance NBD-phallacidin binding without increasing actin nucleation activity. Fractionation studies showed that the nucleation activity in H2O2-treated cells and controls sedimented with the Triton X-100-insoluble cytoskeleton, and the cytosolic fraction appeared to contain an inhibitor of actin polymerization.

摘要

先前的研究表明,过氧化氢会导致细胞内聚合肌动蛋白(F-肌动蛋白)增加。为了验证聚合增加是由肌动蛋白成核活性增加的机制引起的这一假设,我们采用了利用芘标记肌动蛋白的方法来量化细胞裂解物的肌动蛋白成核活性,并通过N-(7-硝基苯并-2-恶唑-1,3-二氮杂-4-基)(NBD)-鬼笔环肽结合试验来量化P388D1细胞中F-肌动蛋白的量。过氧化氢以剂量依赖的方式增加了聚合肌动蛋白(NBD-鬼笔环肽试验),有效剂量产生50%反应(ED50)约为1 mM。5 mM过氧化氢导致NBD-鬼笔环肽染色增加了1.6倍。相比之下,肌动蛋白成核活性以剂量依赖的方式降低,ED50相似。5 mM过氧化氢导致肌动蛋白成核活性降低30 - 40%。这种效应迅速,在添加过氧化氢后5分钟内就会出现。结果表明,过氧化氢会引起细胞骨架变化,增强NBD-鬼笔环肽结合,而不会增加肌动蛋白成核活性。分级分离研究表明,过氧化氢处理细胞和对照中的成核活性与Triton X-100不溶性细胞骨架一起沉淀,并且细胞质部分似乎含有肌动蛋白聚合的抑制剂。

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