| Literature DB >> 28258192 |
Qinqin Pu1,2, Changpei Gan1,2, Rongpeng Li2,3, Yi Li1,2, Shirui Tan2, Xuefeng Li1,2, Yuquan Wei1, Lefu Lan4, Xin Deng5, Haihua Liang6, Feng Ma7, Min Wu8,2.
Abstract
Sepsis is a severe and complicated syndrome that is characterized by dysregulation of host inflammatory responses and organ failure, with high morbidity and mortality. The literature implies that autophagy is a crucial regulator of inflammation in sepsis. In this article, we report that autophagy-related protein 7 (Atg7) is involved in inflammasome activation in Pseudomonas aeruginosa abdominal infection. Following i.p. challenge with P. aeruginosa, atg7fl/fl mice showed impaired pathogen clearance, decreased survival, and widespread dissemination of bacteria into the blood and lung tissue compared with wild-type mice. The septic atg7fl/fl mice also exhibited elevated neutrophil infiltration and severe lung injury. Loss of Atg7 resulted in increased production of IL-1β and pyroptosis, consistent with enhanced inflammasome activation. Furthermore, we demonstrated that P. aeruginosa flagellin is a chief trigger of inflammasome activation in the sepsis model. Collectively, our results provide insight into innate immunity and inflammasome activation in sepsis.Entities:
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Year: 2017 PMID: 28258192 PMCID: PMC5382979 DOI: 10.4049/jimmunol.1601196
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422