4.7 Article

-Adrenergic receptors control brown adipose UCP-1 tone and cold response without affecting its circadian rhythmicity

期刊

FASEB JOURNAL
卷 32, 期 10, 页码 5640-5646

出版社

FEDERATION AMER SOC EXP BIOL
DOI: 10.1096/fj.201800452R

关键词

thermogenesis; locomotor activity; molecular clock; brown adipocytes; Rev-erb

资金

  1. U.S. National Institutes of Health, National Institute of Digestive Diabetes and Kidney Diseases [DK102496, DK45586, F30 DK104513]

向作者/读者索取更多资源

Brown adipose tissue (BAT) thermogenic functions are primarily mediated by uncoupling protein (UCP)-1. Ucp1 gene expression is highly induced by cold temperature, via sympathetic nervous system and -adrenergic receptors (ARs). Ucp1 is also repressed by the clock gene Rev-erb, contributing to its circadian rhythmicity. In this study, we investigated mice lacking ARs (-less mice) to test the relationship between AR signaling and the BAT molecular clock. We found that in addition to controlling the induction of Ucp1 and other key BAT genes at near freezing temperatures, ARs are essential for the basal expression of BAT Ucp1 at room temperature. Remarkably, although basal Ucp1 expression is low throughout day and night in -less mice, the circadian rhythmicity of Ucp1 and clock genes in BAT is maintained. Thus, the requirement of AR signaling for BAT activity is independent of the circadian rhythmicity of Ucp1 expression and circadian oscillation of the molecular clock genes. On the other hand, we found that ARs are essential for the normal circadian rhythms of locomotor activity. Our results demonstrate that in addition to controlling the BAT response to extreme cold, AR signaling is necessary to maintain basal Ucp1 tone and to couple BAT circadian rhythmicity to the central clock.Razzoli, M., Emmett, M. J., Lazar, M. A., Bartolomucci, A. -Adrenergic receptors control brown adipose UCP-1 tone and cold response without affecting its circadian rhythmicity.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据