Oxidative modifications of extracellular matrix promote the second wave of inflammation via β2 integrins.
Ontology highlight
ABSTRACT: Early stages of inflammation are characterized by extensive oxidative insult by recruited and activated neutrophils. Secretion of peroxidases, including the main enzyme, myeloperoxidase, leads to the generation of reactive oxygen species. We show that this oxidative insult leads to polyunsaturated fatty acid (eg, docosahexaenoate), oxidation, and accumulation of its product 2-(ω-carboxyethyl)pyrrole (CEP), which, in turn, is capable of protein modifications. In vivo CEP is generated predominantly at the inflammatory sites in macrophage-rich areas. During thioglycollate-induced inflammation, neutralization of CEP adducts dramatically reduced macrophage accumulation in the inflamed peritoneal cavity while exhibiting no effect on the early recruitment of neutrophils, suggesting a role in the
SUBMITTER: Yakubenko VP
PROVIDER: S-EPMC6034644 | biostudies-literature | 2018 Jul
REPOSITORIES: biostudies-literature
ACCESS DATA