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Priming of neutrophil oxidative burst in diabetes requires preassembly of the NADPH oxidase
Author(s) -
Omori Kazuhiro,
Ohira Taisuke,
Uchida Yushi,
Ayilavarapu Srinivas,
Batista Eraldo L.,
Yagi Motohiko,
Iwata Tomoyuki,
Liu Hongsheng,
Hasturk Hatice,
Kantarci Alpdogan,
Van Dyke Thomas E.
Publication year - 2008
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1189/jlb.1207832
Subject(s) - nadph oxidase , p22phox , respiratory burst , superoxide , oxidative stress , glycation , biology , medicine , endocrinology , receptor , microbiology and biotechnology , biochemistry , enzyme
Hyperglycemia associated with diabetes mellitus results in the priming of neutrophils leading to oxidative stress that is, in part, responsible for diabetic complications. p47 phox , a NADPH oxidase cytosolic subunit, is a key protein in the assembly of the NADPH oxidase leading to superoxide generation. Little is known about the priming mechanism of oxidative pathways in neutrophils of people with diabetes. In this study, the kinetics of p47 phox activation was investigated by comparing neutrophils from diabetic and healthy subjects, and the mechanism of hyperglycemia‐induced changes was studied by using neutrophil‐like HL‐60 cells as a model. In resting neutrophils from diabetic subjects, p47 phox prematurely translocates to the cell membrane and preassembles with p22 phox , a NADPH oxidase membrane subunit. This premature p47 phox translocation and preassembly with p22 phox were also observed in HL‐60 cells cultured with high glucose (HG; 25 mM) and with the specific ligand for the receptor for advanced glycation end products (RAGE), S100B. Phosphorylation of ERK1/2, but not p38 MAPK, was the primary signaling pathway, as evidenced by PD98059 suppressing the translocation of p47 phox in HL‐60 cells incubated with HG and S100B. HL‐60 cells cultured in HG and S100B exhibited a 1.8‐fold increase in fMLP‐induced superoxide generation compared with those cultured in normal glucose (5.5 mM). These data suggest that HG and increased AGE prime neutrophils and increase oxidative stress inducing the translocation of p47 phox to the cell membrane and preassembly with p22 phox by stimulating a RAGE‐ERK1/2 pathway.