Targeting of Rac1 to the Phagocyte Membrane Is Sufficient for the Induction of NADPH Oxidase Assembly

• Published in: The Journal of biological chemistry 2000-12, Vol.275 (51), p.40073-40081
• Main Authors: Gorzalczany, Yara, Sigal, Natalia, Itan, Michal, Lotan, Ofra, Pick, Edgar
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Cell Membrane - metabolism; Enzyme Activation; flavocytochromes; Molecular Sequence Data; NADPH oxidase; NADPH Oxidases - metabolism; Phagocytes - enzymology; Phagocytes - metabolism; phosphatidylcholine; Protein Prenylation; rac1 GTP-Binding Protein - chemistry; rac1 GTP-Binding Protein - metabolism; Rac1 protein
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M006013200

The superoxide (O⨪2)-generating NADPH oxidase complex of phagocytes consists of a membrane-associated flavocytochrome (cytochrome b559) and four cytosolic proteins, p47phox , p67phox , p40phox , and the small GTPase Rac (Rac1 or -2). NADPH oxidase activation (O⨪2 production) is elicited as the consequence of assembly of some or all cytosolic components with cytochromeb559. This process can be reproduced in anin vitro system consisting of phagocyte membranes, p47phox , p67phox , and Rac, activated by an anionic amphiphile. We now show that post-translationally processed (prenylated) Rac1 initiates NADPH oxidase assembly, expressed in O⨪2 production, in a cell-free system containing phagocyte membrane vesicles and p67phox , in the absence of an activating amphiphile and of p47phox . Prenylated Cdc42Hs, a GTPase closely related to Rac, is inactive under the same conditions. Results obtained with phagocyte membrane vesicles can be reproduced fully by replacing these with partially purified cytochrome b559, incorporated in phosphatidylcholine vesicles. Prenylated, but not nonprenylated, Rac1 binds spontaneously to phagocyte membrane vesicles and also to artificial, protein-free, phosphatidylcholine vesicles, a process counteracted by GDP dissociation inhibitor for Rho. Binding of prenylated Rac1 to membrane vesicles is accompanied by the recruitment of p67phox to the same location and the formation of an assembled NADPH oxidase complex, producing O⨪2 upon the addition of NADPH. Amphiphile and p47phox -independent NADPH oxidase activation by prenylated Rac1 is inhibited by Rho GDP dissociation inhibitor and by phosphatidylcholine vesicles, both competing with membrane for prenylated Rac1. We conclude that, in vitro, targeting of Rac to the phagocyte membrane is sufficient for the induction of NADPH oxidase assembly, suggesting that the principal or, possibly, the only role of Rac is to recruit cytosolic p67phox to the membrane environment, to be followed by the interaction of p67phox with cytochromeb559.