Abstract
The neuronal mechanisms that establish 24-hour rhythms in feeding and metabolism remain incompletely understood. In this issue of the JCI, Adlanmerini and colleagues explored the relationship between temporal and homeostatic control of energy balance by focusing on mice that lacked the genes encoding the clock repressor elements REV-ERBαand -β, specifically in the tuberal hypothalamus. Notably, the clock transcription cycle mediated intraneuronal response to the adipostatic hormone leptin. These results show that REV-ERBαand -β in the hypothalamus are necessary for maintaining leptin responsiveness and metabolic homeostasis and lay the foundation to explore how transcriptional changes may link energysensing cell types with day/night rhythms. Such information may lead to therapeutics that alleviate the adverse effects of chronic shift work.
Original language | English (US) |
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Article number | e144655 |
Journal | Journal of Clinical Investigation |
Volume | 131 |
Issue number | 1 |
DOIs | |
State | Published - Jan 4 2021 |
Funding
We acknowledge Biliana Marcheva for help with the figure and support from the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) grants R01DK090625, R01DK100814, 1R01DK113011-01A1, and K99DK124682, the National Institute on Aging (NIA) grants P01AG011412 and R01AG065988 (to JB), the Swedish Research Council grant 2014-6888, and the Swedish Society for Medical Research (to JC).
ASJC Scopus subject areas
- General Medicine