Author: ["Chris D. Ellson","Stéphanie Gobert-Gosse","Karen E Anderson","Keith Davidson","Hediye Erdjument-Bromage","Paul Tempst","Jan W. Thuring","Matthew A. Cooper","Ze-Yi Lim","Andrew B. Holmes","Piers R. J. Gaffney","John Coadwell","Edwin R. Chilvers","Phill T. Hawkins","Len R. Stephens"]
CITE.CC academic search helps you expand the influence of your papers.
Abstract
The production of reactive oxygen species (ROS) by neutrophils has a vital role in defence against a range of infectious agents, and is driven by the assembly of a multi-protein complex containing a minimal core of five proteins: the two membrane-bound subunits of cytochrome b558 (gp91phox and p22phox) and three soluble factors (GTP–Rac, p47phox and p67phox (refs 1, 2). This minimal complex can reconstitute ROS formation in vitro in the presence of non-physiological amphiphiles such as SDS. p40phox has subsequently been discovered as a binding partner for p67phox (ref. 3), but its role in ROS formation is unclear. Phosphoinositide-3-OH kinases (PI(3)Ks) have been implicated in the intracellular signalling pathways coordinating ROS formation4,5 but through an unknown mechanism. We show that the addition of p40phox to the minimal core complex allows a lipid product of PI(3)Ks, phosphatidylinositol 3-phosphate (PtdIns(3)P), to stimulate specifically the formation of ROS. This effect was mediated by binding of PtdIns(3)P to the PX domain6 of p40phox. These results offer new insights into the roles for PI(3)Ks and p40phox in ROS formation and define a cellular ligand for the orphan PX domain.Cite this article
Ellson, C., Gobert-Gosse, S., Anderson, K. et al. PtdIns(3)P regulates the neutrophil oxidase complex by binding to the PX domain of p40phox. Nat Cell Biol 3, 679–682 (2001). https://doi.org/10.1038/35083076 