Details

Autor(en) / Beteiligte

• Belambri, Sahra A.
• Rolas, Loïc
• Raad, Houssam
• Hurtado‐Nedelec, Margarita
• Dang, Pham My‐Chan
• El‐Benna, Jamel

Titel

NADPH oxidase activation in neutrophils: Role of the phosphorylation of its subunits

Ist Teil von

• European journal of clinical investigation, 2018-11, Vol.48 (S2), p.e12951-n/a

Ort / Verlag

England: Blackwell Publishing Ltd

Erscheinungsjahr

2018

Link zum Volltext

Quelle

Wiley Online Library - AutoHoldings Journals

Beschreibungen/Notizen

• Neutrophils are key cells of innate immunity and during inflammation. Upon activation, they produce large amounts of superoxide anion (O2−.) and ensuing reactive oxygen species (ROS) to kill phagocytized microbes. The enzyme responsible for O2−. production is called the phagocyte NADPH oxidase. This is a multicomponent enzyme system that becomes active after assembly of four cytosolic proteins (p47phox, p67phox, p40phox and Rac2) with the transmembrane proteins (p22phox and gp91phox, which form the cytochrome b558). gp91phox represents the catalytic subunit of the NADPH oxidase and is also called NOX2. NADPH oxidase‐derived ROS are essential for microbial killing and innate immunity; however, excessive ROS production induces tissue injury and prolonged inflammatory reactions that contribute to inflammatory diseases. Thus, NADPH oxidase activation must be tightly regulated in time and space to limit ROS production. NADPH oxidase activation is regulated by several processes such as phosphorylation of its components, exchange of GDP/GTP on Rac2 and binding of p47phox and p40phox to phospholipids. This review aims to provide new insights into the role of the phosphorylation of the NADPH oxidase components, that is gp91phox, p22phox, p47phox, p67phox and p40phox, in the activation of this enzyme.