Triiodothyronine (T3) promotes brown fat hyperplasia via thyroid hormone receptor α mediated adipocyte progenitor cell proliferation.
Triiodothyronine (T3) promotes brown fat hyperplasia via thyroid hormone receptor α mediated adipocyte progenitor cell proliferation.
复制标题
三碘甲状腺原氨酸(T3)通过甲状腺激素受体α介导的脂肪细胞祖细胞增殖促进棕色脂肪增生
DOI:
10.1038/s41467-022-31154-1
复制
发表时间:
2022-06-13
影响因子:
16.6
通讯作者:
Ying, Hao
中科院分区:
文献类型:
--
作者:
Liu, Shengnan;Shen, Siyi;Yan, Ying;Sun, Chao;Lu, Zhiqiang;Feng, Hua;Ma, Yiruo;Tang, Zhili;Yu, Jing;Wu, Yuting;Gereben, Balazs;Mohacsik, Petra;Fekete, Csaba;Feng, Xiaoyun;Yuan, Feixiang;Guo, Feifan;Hu, Cheng;Shao, Mengle;Gao, Xin;Zhao, Lin;Li, Yuying;Jiang, Jingjing;Ying, Hao
The thyroid hormone (TH)-controlled recruitment process of brown adipose tissue (BAT) is not fully understood. Here, we show that long-term treatment of T3, the active form of TH, increases the recruitment of thermogenic capacity in interscapular BAT of male mice through hyperplasia by promoting the TH receptor α-mediated adipocyte progenitor cell proliferation. Our single-cell analysis reveals the heterogeneous nature and hierarchical trajectory within adipocyte progenitor cells of interscapular BAT. Further analyses suggest that T3 facilitates cell state transition from a more stem-like state towards a more committed adipogenic state and promotes cell cycle progression towards a mitotic state in adipocyte progenitor cells, through mechanisms involving the action of Myc on glycolysis. Our findings elucidate the mechanisms underlying the TH action in adipocyte progenitors residing in BAT and provide a framework for better understanding of the TH effects on hyperplastic growth and adaptive thermogenesis in BAT depot at a single-cell level. Thyroid hormone (TH) action regulates brown adipose tissue thermogenic capacity through incompletely understood mechanisms. Here the authors report that T3, the active form of TH, increases thermogenic capacity via thyroid hormone receptor α-mediated hyperplasia of brown adipose tissue adipocyte progenitor cells.
登录
查看更多内容
影响因子:
82.9
作者:
Shinoda, Kosaku;Luijten, Ineke H. N.;Hasegawa, Yutaka;Hong, Haemin;Sonne, Si B.;Kim, Miae;Xue, Ruidan;Chondronikola, Maria;Cypess, Aaron M.;Tseng, Yu-Hua;Nedergaard, Jan;Sidossis, Labros S.;Kajimura, Shingo
通讯作者:
Kajimura, Shingo
影响因子:
29
作者:
Martínez-Sánchez N;Seoane-Collazo P;Contreras C;Varela L;Villarroya J;Rial-Pensado E;Buqué X;Aurrekoetxea I;Delgado TC;Vázquez-Martínez R;González-García I;Roa J;Whittle AJ;Gomez-Santos B;Velagapudi V;Tung YCL;Morgan DA;Voshol PJ;Martínez de Morentin PB;López-González T;Liñares-Pose L;Gonzalez F;Chatterjee K;Sobrino T;Medina-Gómez G;Davis RJ;Casals N;Orešič M;Coll AP;Vidal-Puig A;Mittag J;Tena-Sempere M;Malagón MM;Diéguez C;Martínez-Chantar ML;Aspichueta P;Rahmouni K;Nogueiras R;Sabio G;Villarroya F;López M
通讯作者:
López M
DOI:
10.1016/j.bbadis.2013.05.027
发表时间:
2014-03
影响因子:
6.2
作者:
Sanchez-Gurmaches, Joan;Guertin, David A.
通讯作者:
Guertin, David A.
影响因子:
3.9
作者:
Kalinovich, Anastasia V.;de Jong, Jasper M. A.;Nedergaard, Jan
通讯作者:
Nedergaard, Jan
影响因子:
5.5
作者:
Shafer, Maxwell E. R.
通讯作者:
Shafer, Maxwell E. R.