Obesity-induced endoplasmic reticulum stress causes chronic inflammation in adipose tissue

被引:324
作者
Kawasaki, Noritaka [1 ]
Asada, Rie [1 ]
Saito, Atsushi [1 ]
Kanemoto, Soshi [1 ]
Imaizumi, Kazunori [1 ]
机构
[1] Hiroshima Univ, Inst Biomed & Hlth Sci, Dept Biochem, Minami Ku, Hiroshima 7348551, Japan
基金
日本学术振兴会;
关键词
UNFOLDED PROTEIN RESPONSE; KAPPA-B; INSULIN-RESISTANCE; TRANSDUCER OASIS; OXIDATIVE STRESS; FATTY-ACIDS; ER STRESS; ACTIVATION; ACCUMULATION; INVOLVEMENT;
D O I
10.1038/srep00799
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Adipose tissue plays a central role in maintaining metabolic homeostasis under normal conditions. Metabolic diseases such as obesity and type 2 diabetes are often accompanied by chronic inflammation and adipose tissue dysfunction. In this study, we observed that endoplasmic reticulum (ER) stress and the inflammatory response occurred in adipose tissue of mice fed a high-fat diet for a period of 16 weeks. After 16 weeks of feeding, ER stress markers increased and chronic inflammation occurred in adipose tissue. We found that ER stress is induced by free fatty acid (FFA)-mediated reactive oxygen species (ROS) generation and up-regulated gene expression of inflammatory cytokines in 3T3-L1 adipocytes. Oral administration to obese mice of chemical chaperons, which alleviate ER stress, improved chronic inflammation in adipose tissue, followed by the suppression of increased body weight and improved insulin signaling. These results indicate that ER stress plays important pathophysiological roles in obesity-induced adipose tissue dysfunction.
引用
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页数:7
相关论文
共 51 条
[1]   The c-Jun NH2-terminal kinase promotes insulin resistance during association with insulin receptor substrate-1 and phosphorylation of Ser307 [J].
Aguirre, V ;
Uchida, T ;
Yenush, L ;
Davis, R ;
White, MF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (12) :9047-9054
[2]   The Endoplasmic Reticulum Stress Transducer OASIS Is involved in the Terminal Differentiation of Goblet Cells in the Large Intestine [J].
Asada, Rie ;
Saito, Atsushi ;
Kawasaki, Noritaka ;
Kanemoto, Soshi ;
Iwamoto, Hideo ;
Oki, Mami ;
Miyagi, Hidetaka ;
Izumi, Soutarou ;
Imaizumi, Kazunori .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (11) :8144-8153
[3]   The chemical chaperone 4-phenylbutyrate inhibits adipogenesis by modulating the unfolded protein response [J].
Basseri, Sana ;
Lhotak, Sarka ;
Sharma, Arya M. ;
Austin, Richard C. .
JOURNAL OF LIPID RESEARCH, 2009, 50 (12) :2486-2501
[4]   Structure-function analysis of the tertiary bile acid TUDCA for the resolution of endoplasmic reticulum stress in intestinal epithelial cells [J].
Berger, Emanuel ;
Haller, Dirk .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2011, 409 (04) :610-615
[5]   Adipose tissue angiogenesis as a therapeutic target for obesity and metabolic diseases [J].
Cao, Yihai .
NATURE REVIEWS DRUG DISCOVERY, 2010, 9 (02) :107-115
[6]   Endoplasmic reticulum stress, obesity and diabetes [J].
Cnop, Miriam ;
Foufelle, Fabienne ;
Velloso, Licio A. .
TRENDS IN MOLECULAR MEDICINE, 2012, 18 (01) :59-68
[7]   Inflammation and cancer [J].
Coussens, LM ;
Werb, Z .
NATURE, 2002, 420 (6917) :860-867
[8]   Translational repression mediates activation of nuclear factor kappa B by phosphorylated translation initiation factor 2 [J].
Deng, J ;
Lu, PD ;
Zhang, YH ;
Scheuner, D ;
Kaufman, RJ ;
Sonenberg, N ;
Harding, HP ;
Ron, D .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (23) :10161-10168
[9]   Setting the standards: Quality control in the secretory pathway [J].
Ellgaard, L ;
Molinari, M ;
Helenius, A .
SCIENCE, 1999, 286 (5446) :1882-1888
[10]  
Furukawa S., 2004, Journal of Clinical Investigation, V114, P1752, DOI 10.1172/JCI21625