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Kawai T , Autieri MV , Scalia R
Adipose Tissue Inflammation and Metabolic Dysfunction in Obesity
Am J Physiol Cell Physiol. 2021 Mar 1;320(3) :C375-C391
PMID: 33356944 URL: https://www.ncbi.nlm.nih.gov/pubmed/33356944
AbstractSeveral lines of preclinical and clinical research have confirmed that chronic low-grade inflammation of adipose tissue is mechanistically linked to metabolic disease and organ tissue complications in the overweight and obese organism. Despite this widely confirmed paradigm, numerous open questions and knowledge gaps remain to be investigated. This is mainly due to the intricately intertwined crosstalk of various pro- and anti- inflammatory signaling cascades involved in the immune response of expanding adipose depots, particularly the visceral adipose tissue. Adipose Tissue inflammation is initiated and sustained over time by dysfunctional adipocytes that secrete inflammatory adipokines and by infiltration of bone-marrow derived immune cells that signal via production of cytokines and chemokines. Despite its low-grade nature, adipose tissue inflammation negatively impacts remote organ function, a phenomenon that is considered causative of the complications of obesity. The aim of this review is to broadly present an overview of adipose tissue inflammation by highlighting the most recent reports in the scientific literature and summarizing our overall understanding of the field. We also discuss key endogenous antiinflammatory mediators and analyze their mechanistic role(s) in the pathogenesis and treatment of adipose tissue inflammation. In doing so, we hope to stimulate studies to uncover novel physiologic, cellular, and molecular targets for the treatment of obesity.
Notes1522-1563 Kawai, Tatsuo Autieri, Michael V Scalia, Rosario DK096521/HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)/ HL141108/HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI)/ HL117724/HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI)/ Journal Article United States Am J Physiol Cell Physiol. 2020 Dec 23. doi: 10.1152/ajpcell.00379.2020.