microRNAs as a New Mechanism Regulating Adipose Tissue Inflammation in Obesity and as a Novel Therapeutic Strategy in the Metabolic Syndrome

被引:69
作者
Ge, Qian [1 ]
Brichard, Sonia [2 ]
Yi, Xu [3 ]
Li, QiFu [1 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 1, Dept Endocrinol, Chongqing 400016, Peoples R China
[2] Univ Louvain, Inst Expt & Clin Res, Endocrinol Diabet & Nutr Unit, Med Sect, B-1200 Brussels, Belgium
[3] Third Mil Med Univ, Daping Hosp, Inst Surg Res, Neurol Unit, Chongqing 400042, Peoples R China
关键词
TOLL-LIKE RECEPTORS; INSULIN-RESISTANCE; CELL DEVELOPMENT; GENE-EXPRESSION; INNATE IMMUNITY; HYPOXIA; STRESS; MICE; ADIPOGENESIS; ENDOTOXEMIA;
D O I
10.1155/2014/987285
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Obesity is associated closely with the metabolic syndrome ( MS). It is well known that obesity-induced chronic inflammation plays a fundamental role in the pathogenesis of MS. White adipose tissue ( AT) is the primary site for the initiation and exacerbation of obesity-associated inflammation. Exploring the mechanisms of white AT inflammation and resetting the immunological balance in white AT could be crucial for the management of MS. Several prominent molecular mechanisms have been proposed to mediate inflammation in white AT, including hypoxia, endoplasmic reticulum stress, lipotoxicity, and metabolic endotoxemia. Recently, a growing body of evidence supports the role of miRNAs as a new important inflammatory mediator by regulating both the adaptive and innate immunity. This review will focus on the implication of miRNAs in white AT inflammation in obesity, and will also highlight the potential of miRNAs as targets for therapeutic intervention in MS as well as the challenges lying in miRNA-targeting therapeutics.
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页数:10
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