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p21rac2从胞质溶胶向质膜的易位对于中性粒细胞NADPH氧化酶活性既非必要条件也非充分条件。

Translocation of p21rac2 from cytosol to plasma membrane is neither necessary nor sufficient for neutrophil NADPH oxidase activity.

作者信息

Philips M R, Feoktistov A, Pillinger M H, Abramson S B

机构信息

Department of Medicine, New York University School of Medicine, New York 10016, USA.

出版信息

J Biol Chem. 1995 May 12;270(19):11514-21. doi: 10.1074/jbc.270.19.11514.

Abstract

Activation of the membrane-associated NADPH oxidase of neutrophils requires several cytosolic factors including p47phox, p67phox and p21rac2. We compared NADPH oxidase activity with the membrane translocation of p47phox, p67phox, and p21rac2. In a cell-free system, GTP gamma S stimulated translocation of p47phox and p67phox to the plasma membrane only in the presence of arachidonate, and this translocation correlated with NADPH oxidase activity of the reisolated plasma membranes (R = 0.94 and 0.97, respectively). In contrast, GTP gamma S-stimulated p21rac2 translocation with or without arachidonate, and the extent of translocation did not correlate with oxidase activity (R = 0.17). Neutrophil cytoplasts were used to relate membrane translocation of p47phox, p67phox and p21rac2 to membrane oxidase activity in response to the inflammatory agonists. Whereas N-formyl-methionyl-leucyl-phenylalanine stimulated equimolar, transient membrane translocation of p47phox and p67phox which kinetically paralleled NADPH oxidase activity, relatively little p21rac2 translocated (moles of p47phox/p21rac2 = 16.6). Moreover, although phorbol 12-myristate 13-acetate stimulated both the stable translocation of p47phox and p67phox and sustained NADPH oxidase activity, it did not stimulate p21rac2 translocation. From these data we conclude that membrane translocation of p21rac2 does not regulate NADPH oxidase activity stoichiometrically.

摘要

中性粒细胞膜相关NADPH氧化酶的激活需要几种胞质因子,包括p47phox、p67phox和p21rac2。我们将NADPH氧化酶活性与p47phox、p67phox和p21rac2的膜转位进行了比较。在无细胞体系中,只有在花生四烯酸存在的情况下,GTPγS才会刺激p47phox和p67phox转位至质膜,且这种转位与重新分离的质膜的NADPH氧化酶活性相关(相关系数R分别为0.94和0.97)。相比之下,无论有无花生四烯酸,GTPγS均能刺激p21rac2转位,但其转位程度与氧化酶活性无关(相关系数R = 0.17)。利用中性粒细胞胞质体来研究p47phox、p67phox和p21rac2的膜转位与炎症激动剂刺激下的膜氧化酶活性之间的关系。N-甲酰甲硫氨酰亮氨酰苯丙氨酸刺激p47phox和p67phox等摩尔的瞬时膜转位,其动力学与NADPH氧化酶活性平行,而p21rac2的转位相对较少(p47phox/p21rac2的摩尔比 = 16.6)。此外,尽管佛波酯12-肉豆蔻酸酯13-乙酸盐能刺激p47phox和p67phox的稳定转位以及持续的NADPH氧化酶活性,但它并不能刺激p21rac2转位。根据这些数据我们得出结论,p21rac2的膜转位不能按化学计量调节NADPH氧化酶活性。

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