期刊
CELL METABOLISM
卷 12, 期 6, 页码 580-592出版社
CELL PRESS
DOI: 10.1016/j.cmet.2010.11.002
关键词
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资金
- Nutrigenomics Consortium, TI Food and Nutrition, Netherlands Heart Foundation [2007B046]
- Netherlands Organisation for Scientific Research [40-00812-98-08030]
- National Institutes of Health [R01DK082582]
- American Diabetes Association [7-08-JF-47]
Dietary saturated fat is linked to numerous chronic diseases, including cardiovascular disease. Here we study the role of the lipoprotein lipase inhibitor AngptI4 in the response to dietary saturated fat. Strikingly, in mice lacking AngptI4, saturated fat induces a severe and lethal phenotype characterized by fibrinopurulent peritonitis, ascites, intestinal fibrosis, and cachexia. These abnormalities are preceded by a massive acute phase response induced by saturated but not unsaturated fat or medium-chain fat, originating in mesenteric lymph nodes (MLNs). MLNs undergo dramatic expansion and contain numerous lipid-laden macrophages. In peritoneal macrophages incubated with chyle, AngptI4 dramatically reduced foam cell formation, inflammatory gene expression, and chyle-induced activation of ER stress. Induction of macrophage AngptI4 by fatty acids is part of a mechanism that serves to reduce postprandial lipid uptake from chyle into MLN-resident macrophages by inhibiting triglyceride hydrolysis, thereby preventing macrophage activation and foam cell formation and protecting against progressive, uncontrolled saturated fat-induced inflammation.
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