Peroxisomal regulation of redox homeostasis and adipocyte metabolism

被引:36
作者
Liu, Jingjing [1 ]
Lu, Wen [1 ,2 ]
Shi, Bimin [2 ]
Klein, Samuel [3 ]
Su, Xiong [1 ,3 ]
机构
[1] Soochow Univ, Dept Biochem & Mol Biol, Coll Med, Suzhou 215123, Peoples R China
[2] Soochow Univ, Affiliated Hosp 1, Dept Endocrinol, Suzhou 215006, Peoples R China
[3] Washington Univ, Sch Med, Ctr Human Nutr, St Louis, MO 63110 USA
来源
REDOX BIOLOGY | 2019年 / 24卷
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
Peroxisomes; Redox; Lipid metabolism; Adipocytes; Mitochondria; OXIDATIVE STRESS; ADIPOSE-TISSUE; WHITE ADIPOCYTE; S-NITROSYLATION; ETHER LIPIDS; OBESITY; DIFFERENTIATION; MITOCHONDRIA; TARGETS; THERMOGENESIS;
D O I
10.1016/j.redox.2019.101167
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Peroxisomes are ubiquitous cellular organelles required for specific pathways of fatty acid oxidation and lipid synthesis, and until recently their functions in adipocytes have not been well appreciated. Importantly, peroxisomes host many oxygen-consumption reactions and play a major role in generation and detoxification of reactive oxygen species (ROS) and reactive nitrogen species (RNS), influencing whole cell redox status. Here, we review recent progress in peroxisomal functions in lipid metabolism as related to ROS/RNS metabolism and discuss the roles of peroxisomal redox homeostasis in adipogenesis and adipocyte metabolism. We provide a framework for understanding redox regulation of peroxisomal functions in adipocytes together with testable hypotheses for developing therapies for obesity and the related metabolic diseases.
引用
收藏
页数:8
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