Browning of white fat: agents and implications for beige adipose tissue to type 2 diabetes

被引:165
作者
Kaisanlahti, A. [1 ]
Glumoff, T. [2 ]
机构
[1] Univ Oulu, Bioctr Oulu, Canc Res & Translat Med, Res Unit, Aapistie 5,POB 5281, Oulu 90014, Finland
[2] Univ Oulu, Fac Biochem & Mol Med, Aapistie 7A,POB 5400, Oulu 90014, Finland
关键词
Brown adipose tissue; Beige adipose tissue; Type; 2; diabetes; Browning; DIET-INDUCED OBESITY; PPAR-GAMMA ACTIVATION; MITOCHONDRIAL BIOGENESIS; UNCOUPLING PROTEIN-1; INSULIN-RESISTANCE; GLUCOSE-UPTAKE; ADIPOCYTES; THERMOGENESIS; ADIPOGENESIS; EXPRESSION;
D O I
10.1007/s13105-018-0658-5
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
Mammalian adipose tissue is traditionally categorized into white and brown relating to their function and morphology: while white serves as an energy storage, brown adipose tissue acts as the heat generator maintaining the core body temperature. The most recently identified type of fat, beige adipocyte tissue, resembles brown fat by morphology and function but is developmentally more related to white. The synthesis of beige fat, so-called browning of white fat, has developed into a topical issue in diabetes and metabolism research. This is due to its favorable effect on whole-body energy metabolism and the fact that it can be recruited during adult life. Indeed, brown and beige adipose tissues have been demonstrated to play a role in glucose homeostasis, insulin sensitivity, and lipid metabolismall factors related to pathogenesis of type 2 diabetes. Many agents capable of initiating browning have been identified so far and tested widely in humans and animal models including in vitro and in vivo experiments. Interestingly, several agents demonstrated to have browning activity are in fact secreted as adipokines from brown and beige fat tissue, suggesting a physiological relevance both in beige adipocyte recruitment processes and in maintenance of metabolic homeostasis. The newest findings on agents driving beige fat recruitment, their mechanisms, and implications on type 2 diabetes are discussed in this review.
引用
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页码:1 / 10
页数:10
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