Myeloid-specific SIRT1 Deletion Aggravates Hepatic Inflammation and Steatosis in High-fat Diet-fed Mice.
10.4196/kjpp.2015.19.5.451
- Author:
Kyung Eun KIM
1
;
Hwajin KIM
;
Rok Won HEO
;
Hyun Joo SHIN
;
Chin Ok YI
;
Dong Hoon LEE
;
Hyun Joon KIM
;
Sang Soo KANG
;
Gyeong Jae CHO
;
Wan Sung CHOI
;
Gu Seob ROH
Author Information
1. Department of Anatomy and Convergence Medical Science, Institute of Health Sciences, Gyeongsang National University School of Medicine, Jinju 660-751, Korea. anaroh@gnu.ac.kr
- Publication Type:Original Article
- Keywords:
Hepatic steatosis;
High-fat diet;
Nuclear factor kappa B;
Sirtuin 1
- MeSH:
Acetylation;
Actins;
Animals;
Collagen;
Connective Tissue Growth Factor;
Diet;
Diet, High-Fat;
Fibrosis;
Glucose;
Inflammation*;
Insulin Resistance;
Liver;
Macrophages;
Metabolism;
Mice*;
NF-kappa B;
Obesity;
Sirtuin 1;
Sterol Regulatory Element Binding Protein 1;
Weight Gain
- From:The Korean Journal of Physiology and Pharmacology
2015;19(5):451-460
- CountryRepublic of Korea
- Language:English
-
Abstract:
Sirtuin 1 (SIRT1) is a mammalian NAD+-dependent protein deacetylase that regulates cellular metabolism and inflammatory response. The organ-specific deletion of SIRT1 induces local inflammation and insulin resistance in dietary and genetic obesity. Macrophage-mediated inflammation contributes to insulin resistance and metabolic syndrome, however, the macrophage-specific SIRT1 function in the context of obesity is largely unknown. C57/BL6 wild type (WT) or myeloid-specific SIRT1 knockout (KO) mice were fed a high-fat diet (HFD) or normal diet (ND) for 12 weeks. Metabolic parameters and markers of hepatic steatosis and inflammation in liver were compared in WT and KO mice. SIRT1 deletion enhanced HFD-induced changes on body and liver weight gain, and increased glucose and insulin resistance. In liver, SIRT1 deletion increased the acetylation, and enhanced HFD-induced nuclear translocation of nuclear factor kappa B (NF-kappaB), hepatic inflammation and macrophage infiltration. HFD-fed KO mice showed severe hepatic steatosis by activating lipogenic pathway through sterol regulatory element-binding protein 1 (SREBP-1), and hepatic fibrogenesis, as indicated by induction of connective tissue growth factor (CTGF), alpha-smooth muscle actin (alpha-SMA), and collagen secretion. Myeloid-specific deletion of SIRT1 stimulates obesity-induced inflammation and increases the risk of hepatic fibrosis. Targeted induction of macrophage SIRT1 may be a good therapy for alleviating inflammation-associated metabolic syndrome.
