Adipocyte Inflammation Is Essential for Healthy Adipose Tissue Expansion and Remodeling

被引:583
作者
Asterholm, Ingrid Wernstedt [1 ]
Tao, Caroline [1 ]
Morley, Thomas S. [1 ]
Wang, Qiong A. [1 ]
Delgado-Lopez, Fernando [3 ]
Wang, Zhao V. [1 ]
Scherer, Philipp E. [1 ,2 ]
机构
[1] UT Southwestern Med Ctr, Touchstone Diabet Ctr, Dept Internal Med, Dallas, TX 75390 USA
[2] UT Southwestern Med Ctr, Dept Cell Biol, Dallas, TX 75390 USA
[3] Univ Catolica Maule, Fac Med, Talca, Chile
基金
瑞典研究理事会; 美国国家卫生研究院;
关键词
NECROSIS-FACTOR-ALPHA; INSULIN-RESISTANCE; IDENTIFICATION; EXPRESSION; OBESITY; FAT; DIFFERENTIATION; ADIPOGENESIS; HOMEOSTASIS; PROGRESSION;
D O I
10.1016/j.cmet.2014.05.005
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Chronic inflammation constitutes an important link between obesity and its pathophysiological sequelae. In contrast to the belief that inflammatory signals exert a fundamentally negative impact on metabolism, we show that proinflammatory signaling in the adipocyte is in fact required for proper adipose tissue remodeling and expansion. Three mouse models with an adipose tissue-specific reduction in proinflammatory potential were generated that display a reduced capacity for adipogenesis in vivo, while the differentiation potential is unaltered in vitro. Upon high-fat-diet exposure, the expansion of visceral adipose tissue is prominently affected. This is associated with decreased intestinal barrier function, increased hepatic steatosis, and metabolic dysfunction. An impaired local proinflammatory response in the adipocyte leads to increased ectopic lipid accumulation, glucose intolerance, and systemic inflammation. Adipose tissue inflammation is therefore an adaptive response that enables safe storage of excess nutrients and contributes to a visceral depot barrier that effectively filters gut-derived endotoxin.
引用
收藏
页码:103 / 118
页数:16
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