| Literature DB >> 26603191 |
Andrew J Murphy1, Michael J Kraakman2, Helene L Kammoun3, Dragana Dragoljevic1, Man K S Lee1, Kate E Lawlor4, John M Wentworth5, Ajithkumar Vasanthakumar6, Motti Gerlic7, Lachlan W Whitehead8, Ladina DiRago9, Louise Cengia9, Rachael M Lane10, Donald Metcalf11, James E Vince4, Leonard C Harrison5, Axel Kallies6, Benjamin T Kile12, Ben A Croker13, Mark A Febbraio14, Seth L Masters15.
Abstract
Interleukin-18 (IL-18) is activated by Caspase-1 in inflammasome complexes and has anti-obesity effects; however, it is not known which inflammasome regulates this process. We found that mice lacking the NLRP1 inflammasome phenocopy mice lacking IL-18, with spontaneous obesity due to intrinsic lipid accumulation. This is exacerbated when the mice are fed a high-fat diet (HFD) or a high-protein diet, but not when mice are fed a HFD with low energy density (high fiber). Furthermore, mice with an activating mutation in NLRP1, and hence increased IL-18, have decreased adiposity and are resistant to diet-induced metabolic dysfunction. Feeding these mice a HFD further increased plasma IL-18 concentrations and strikingly resulted in loss of adipose tissue mass and fatal cachexia, which could be prevented by genetic deletion of IL-18. Thus, NLRP1 is an innate immune sensor that functions in the context of metabolic stress to produce IL-18, preventing obesity and metabolic syndrome.Entities:
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Year: 2015 PMID: 26603191 DOI: 10.1016/j.cmet.2015.09.024
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287