| ISX-9 potentiates CaMKII delta-mediated BMAL1 activation to enhance circadian amplitude |
| 論文作者 |
Li, HL; Ou, JL; Li, YQ; Xu, NN; Li, Q; Wu, P; Peng, C; Tang, YC; Chang, HC |
| 期刊/會(huì)議名稱 |
COMMUNICATIONS BIOLOGY |
| 論文年度 |
2022 |
| 論文類別 |
Article |
| 摘要 |
Circadian dysregulation associates with numerous diseases including metabolic dysfunction, sleep disorder, depression and aging. Given that declined circadian amplitude is a trait commonly found with compromised health, interventions that design in precluding circadian amplitude from dampening will aid to mitigate complex, circadian-related diseases. Here we identify a neurogenic small molecule ISX-9 that is able to support persistent and higher amplitude of circadian oscillations. ISX-9 improves diurnal metabolic rhythms in middle-aged mice. Moreover, the ISX-9-treated mice show better sleep homeostasis with increased delta power during the day time and higher locomotive activity in the dark period. ISX-9 augments CaMKII delta expression and increases BMAL1 activity via eliciting CaMKII delta-mediated phosphorylation on BMAL1 residues S513/S515/S516, accordingly composes a positive feedback effect on enhancing circadian amplitude. CaMKII delta-targeting, and the use of ISX-9 may serve as decent choices for treating circadian-related disorders. Circadian modulators that exert amplitude-enhancing activity using highthroughput compound screening of small molecules identifies ISX-9, which is shown to augment CaMKII delta expression, increasing BMAL1 activity via CaMKII delta-dependent phosphorylation. |
| 期 |
1 |
| 卷 |
5 |
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