Exploring the In Vivo Role of the Mitochondrial Calcium Uniporter in Brown Fat Bioenergetics

被引:39
作者
Flicker, Daniel [1 ,2 ,3 ,4 ]
Sancak, Yasemin [1 ,2 ,3 ,4 ,5 ]
Mick, Eran [1 ,2 ,3 ,4 ]
Goldberger, Olga [1 ,2 ,3 ,4 ]
Mootha, Vamsi K. [1 ,2 ,3 ,4 ]
机构
[1] Massachusetts Gen Hosp, Howard Hughes Med Inst, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA
[3] Harvard Med Sch, Dept Syst Biol, Boston, MA 02115 USA
[4] Broad Inst, Cambridge, MA 02141 USA
[5] Univ Washington, Sch Med, Dept Pharmacol, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
GLUTATHIONE TRANSFERASE A3-3; INTEGRATED STRESS-RESPONSE; DIET-INDUCED THERMOGENESIS; ADIPOSE-TISSUE; SKELETAL-MUSCLE; ENDOPLASMIC-RETICULUM; ESSENTIAL COMPONENT; NEGATIVE-FEEDBACK; BEIGE ADIPOCYTES; CA2+ RELEASE;
D O I
10.1016/j.celrep.2019.04.013
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mitochondrial calcium uniporter has been proposed to coordinate the organelle's energetics with calcium signaling. Uniporter current has previously been reported to be extremely high in brown adipose tissue (BAT), yet it remains unknown how the uniporter contributes to BAT physiology. Here, we report the generation and characterization of a mouse model lacking Mcu, the pore forming subunit of the uniporter, specifically in BAT(BAT-Mcu-KO). BAT-Mcu-KO mice lack uniporter-based calcium uptake in BAT mitochondria but exhibit unaffected cold tolerance, diet-induced obesity, and transcriptional response to cold in BAT. Unexpectedly, we found in wild-type animals that cold powerfully activates the ATF4-dependent integrated stress response (ISR) in BAT and upregulates circulating FGF21 and GDF15, raising the hypothesis that the ISR partly underlies the pleiotropic effects of BAT on systemic metabolism. Our study demonstrates that the uniporter is largely dispensable for BAT thermogenesis and demonstrates activation of the ISR in BAT in response to cold.
引用
收藏
页码:1364 / +
页数:17
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