| Literature DB >> 22447028 |
Mehmet A Eskan1, Ravi Jotwani, Toshiharu Abe, Jindrich Chmelar, Jong-Hyung Lim, Shuang Liang, Paul A Ciero, Jennifer L Krauss, Fenge Li, Martina Rauner, Lorenz C Hofbauer, Eun Young Choi, Kyoung-Jin Chung, Ahmed Hashim, Michael A Curtis, Triantafyllos Chavakis, George Hajishengallis.
Abstract
Aging is linked to greater susceptibility to chronic inflammatory diseases, several of which, including periodontitis, involve neutrophil-mediated tissue injury. Here we found that aging-associated periodontitis was accompanied by lower expression of Del-1, an endogenous inhibitor of neutrophil adhesion dependent on the integrin LFA-1, and by reciprocal higher expression of interleukin 17 (IL-17). Consistent with that, IL-17 inhibited gingival endothelial cell expression of Del-1, thereby promoting LFA-1-dependent recruitment of neutrophils. Young Del-1-deficient mice developed spontaneous periodontitis that featured excessive neutrophil infiltration and IL-17 expression; disease was prevented in mice doubly deficient in Del-1 and LFA-1 or in Del-1 and the IL-17 receptor. Locally administered Del-1 inhibited IL-17 production, neutrophil accumulation and bone loss. Therefore, Del-1 suppressed LFA-1-dependent recruitment of neutrophils and IL-17-triggered inflammatory pathology and may thus be a promising therapeutic agent for inflammatory diseases.Entities:
Mesh:
Substances:
Year: 2012 PMID: 22447028 PMCID: PMC3330141 DOI: 10.1038/ni.2260
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606