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蛋白激酶D参与中性粒细胞中NADPH氧化酶的Fcγ受体激活过程。

Involvement of protein kinase D in Fc gamma-receptor activation of the NADPH oxidase in neutrophils.

作者信息

Davidson-Moncada Jan K, Lopez-Lluch Guillermo, Segal Anthony W, Dekker Lodewijk V

机构信息

Centre for Molecular Medicine, Department of Medicine, University College London, The Rayne Institute, 5 University Street, London WC1E 6JJ, UK.

出版信息

Biochem J. 2002 Apr 1;363(Pt 1):95-103. doi: 10.1042/0264-6021:3630095.

Abstract

Protein kinases involved in the activation of the NADPH oxidase by Fc gamma receptors in neutrophils were studied. Of three different protein kinase C (PKC) inhibitors, Gö 6976 inhibited the NADPH oxidase completely, whereas bisindolylmaleimide I and Ro 31-8220 caused a 70-80% inhibition. Thus a Gö 6976-sensitive, bisindolylmaleimide I/Ro 31-8220-insensitive component contributes to NADPH oxidase activation induced by Fc gamma receptors. Down-regulation of PKC isotypes resulted in inhibition of Fc gamma-receptor-activated NADPH oxidase, but a down-regulation-insensitive component was still present. This component was sensitive to Gö 6976, but insensitive to Ro 31-8220. It has been shown previously that protein kinase D/PKC-mu (PKD) shows this same pharmacology in vitro. We show that PKD is present in neutrophils and that, in contrast with PKC isotypes, PKD is not down-regulated. Therefore PKD may participate in NADPH oxidase activation. To obtain direct evidence for this we adopted an antisense approach. Antisense PKD inhibited NADPH oxidase induced by Fc gamma-receptor stimulation by 50% and the Ro 31-8220-insensitive component in the activation was inhibited by antisense PKD. In vitro kinase assays showed that PKD is activated by presenting IgG-opsonized particles to neutrophils. Furthermore, PKD localizes to the area of particle intake in the cell and phosphorylates two of the three cytosolic components of the NADPH oxidase, p40(phox) and p47(phox). Taken together, these data indicate that Fc gamma receptors engage PKD in the regulation of the NADPH oxidase.

摘要

研究了参与中性粒细胞中Fcγ受体激活NADPH氧化酶的蛋白激酶。在三种不同的蛋白激酶C(PKC)抑制剂中,Gö 6976完全抑制了NADPH氧化酶,而双吲哚马来酰亚胺I和Ro 31-8220则导致70-80%的抑制。因此,一种对Gö 6976敏感、对双吲哚马来酰亚胺I/Ro 31-8220不敏感的成分有助于Fcγ受体诱导的NADPH氧化酶激活。PKC同工型的下调导致Fcγ受体激活的NADPH氧化酶受到抑制,但仍存在一个对下调不敏感的成分。该成分对Gö 6976敏感,但对Ro 31-8220不敏感。先前已表明,蛋白激酶D/PKC-μ(PKD)在体外表现出相同的药理学特性。我们发现PKD存在于中性粒细胞中,并且与PKC同工型不同,PKD不会被下调。因此,PKD可能参与NADPH氧化酶的激活。为了获得直接证据,我们采用了反义方法。反义PKD抑制Fcγ受体刺激诱导的NADPH氧化酶达50%,并且激活过程中对Ro 31-8220不敏感的成分也被反义PKD抑制。体外激酶分析表明,向中性粒细胞呈现IgG调理颗粒可激活PKD。此外,PKD定位于细胞内颗粒摄取区域,并使NADPH氧化酶的三个胞质成分中的两个,即p40(phox)和p47(phox)磷酸化。综上所述,这些数据表明Fcγ受体通过PKD参与NADPH氧化酶的调节。

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