Brown adipose tissue as an endocrine organ: updates on the emerging role of batokines

被引:12
作者
Martins, Fabiane Ferreira [1 ]
Souza-Mello, Vanessa [1 ]
Aguila, Marcia Barbosa [1 ]
Mandarim-de-Lacerda, Carlos Alberto [1 ]
机构
[1] Univ Estado Rio de Janeiro, Ctr Biomed, Inst Biol, Lab Morfometria Metab & Doenca Cardiovasc, Av 28 Setembro 87 Fds, BR-20551030 Rio De Janeiro, RJ, Brazil
关键词
batokines; bone morphogenetic protein 8; fibroblast growth factor-21; neuregulin; 4; vascular endothelial growth factor A; ENDOTHELIAL GROWTH-FACTOR; GENE-EXPRESSION; THERMOGENESIS; ADIPOGENESIS; INFLAMMATION; HOMEOSTASIS; MYOSTATIN; OREXIN; BMP8B; MICE;
D O I
10.1515/hmbci-2022-0044
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
Brown adipose tissue (BAT) remains active in adults, oxidizing fatty acids or glucose and releasing energy in the form of heat. Brown adipocytes and enhanced thermogenesis are targets for treating obesity and its comorbidities. BAT shows high synthesis activity and secretes several signaling molecules. The brown adipokines, or batokines, take action in an autocrine, paracrine, and endocrine manner. Batokines have a role in the homeostasis of the cardiovascular system, central nervous system, white adipose tissue, liver, and skeletal muscle and exert beneficial effects on BAT. The systemic function of batokines gives BAT an endocrine organ profile. Besides, the batokines Fibroblast Growth Factor-21, Vascular Endothelial Growth Factor A, Bone Morphogenetic Protein 8, Neuregulin 4, Myostatin, and Interleukin-6 emerge as targets to treat obesity and its comorbidities, deserving attention. This review outlines the role of six emerging batokines on BAT and their cross-talk with other organs, focusing on their physiological significance and diet-induced changes.
引用
收藏
页码:219 / 227
页数:9
相关论文
共 75 条
[21]   FGF21 ameliorates the neurocontrol of blood pressure in the high fructose-drinking rats [J].
He, Jian-Li ;
Zhao, Miao ;
Xia, Jing-Jun ;
Guan, Jian ;
Liu, Yang ;
Wang, Lu-Qi ;
Song, Dong-Xue ;
Qu, Mei-Yu ;
Zuo, Meng ;
Wen, Xin ;
Yu, Xue ;
Huo, Rong ;
Pan, Zhen-Wei ;
Ban, Tao ;
Zhang, Yan ;
Zhu, Jiu-Xin ;
Shou, Weinian ;
Qiao, Guo-Fen ;
Li, Bai-Yan .
SCIENTIFIC REPORTS, 2016, 6
[22]   UCP1 Dependent and Independent Thermogenesis in Brown and Beige Adipocytes [J].
Ikeda, Kenji ;
Yamada, Tetsuya .
FRONTIERS IN ENDOCRINOLOGY, 2020, 11
[23]   Brown and Beige Fat: Physiological Roles beyond Heat Generation [J].
Kajimura, Shingo ;
Spiegelman, Bruce M. ;
Seale, Patrick .
CELL METABOLISM, 2015, 22 (04) :546-559
[24]   Muscle, Bone, and Fat Crosstalk: the Biological Role of Myokines, Osteokines, and Adipokines [J].
Kirk, Ben ;
Feehan, Jack ;
Lombardi, Giovanni ;
Duque, Gustavo .
CURRENT OSTEOPOROSIS REPORTS, 2020, 18 (04) :388-400
[25]   Brown Adipose Tissue Controls Skeletal Muscle Function via the Secretion of Myostatin [J].
Kong, Xingxing ;
Yao, Ting ;
Zhou, Peng ;
Kazak, Lawrence ;
Tenen, Danielle ;
Lyubetskaya, Anna ;
Dawes, Brian A. ;
Tsai, Linus ;
Kahn, Barbara B. ;
Spiegelman, Bruce M. ;
Liu, Tiemin ;
Rosen, Evan D. .
CELL METABOLISM, 2018, 28 (04) :631-+
[26]  
Korac A, 2008, HISTOL HISTOPATHOL, V23, P441, DOI 10.14670/HH-23.441
[27]   PPARγ and PPARα synergize to induce robust browning of white fat in vivo [J].
Kroon, Tobias ;
Harms, Matthew ;
Maurer, Stefanie ;
Bonnet, Laurianne ;
Alexandersson, Ida ;
Lindblom, Anna ;
Ahnmark, Andrea ;
Nilsson, Daniel ;
Gennemark, Peter ;
O'Mahony, Gavin ;
Osinski, Victoria ;
McNamara, Coleen ;
Boucher, Jeremie .
MOLECULAR METABOLISM, 2020, 36
[28]   Induction of uncoupling protein 1 by central interleukin-6 gene delivery is dependent on sympathetic innervation of brown adipose tissue and underlies one mechanism of body weight reduction in rats [J].
Li, G ;
Klein, RL ;
Matheny, M ;
King, MA ;
Meyer, EM ;
Scarpace, PJ .
NEUROSCIENCE, 2002, 115 (03) :879-889
[29]   Peripheral IL-6/STAT3 signaling promotes beiging of white fat [J].
Li, Haifang ;
Dong, Mei ;
Liu, Wenhui ;
Gao, Cheng ;
Jia, Yanxin ;
Zhang, Xinzhi ;
Xiao, Xue ;
Liu, Qingxin ;
Lin, Hai .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2021, 1868 (10)
[30]   Fibroblast growth factor 21 inhibited inflammation and fibrosis after myocardial infarction via EGR1 [J].
Li, Jiamin ;
Gong, Liling ;
Zhang, Ruijie ;
Li, Sijia ;
Yu, Hang ;
Liu, Yining ;
Xue, Yadong ;
Huang, Di ;
Xu, Ning ;
Wang, Ying ;
Xu, Yan ;
Zhao, Yiming ;
Li, Qingsui ;
Li, Ming ;
Li, Pengyu ;
Liu, Mingbin ;
Zhang, Zhen ;
Li, Xin ;
Du, Weijie ;
Wang, Ning .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2021, 910