Circadian regulation of dentate gyrus excitability mediated by G-protein signaling

被引:10
|
作者
Gonzalez, Jose Carlos [1 ,2 ]
Lee, Haeun [1 ,2 ]
Vincent, Angela M. [1 ,2 ]
Hill, Angela L. [1 ,2 ]
Goode, Lacy K. [3 ]
King, Gwendalyn D. [4 ]
Gamble, Karen L. [3 ]
Wadiche, I.
Wadiche, Jacques I. [1 ,2 ]
Overstreet-Wadiche, Linda [1 ,2 ]
机构
[1] Univ Alabama Birmingham, Dept Neurobiol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, McKnight Brain Inst, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Dept Psychiat & Behav Neurobiol, Birmingham, AL 35294 USA
[4] Creighton Univ, Dept Biol, Omaha, NE 68178 USA
来源
CELL REPORTS | 2023年 / 42卷 / 02期
关键词
GRANULE CELLS; CHANNEL; SLEEP; ACTIVATION; CURRENTS; SPARSE; MARKER; WAKE;
D O I
10.1016/j.celrep.2023.112039
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The central circadian regulator within the suprachiasmatic nucleus transmits time of day information by a diurnal spiking rhythm driven by molecular clock genes controlling membrane excitability. Most brain re-gions, including the hippocampus, harbor similar intrinsic circadian transcriptional machinery, but whether these molecular programs generate oscillations of membrane properties is unclear. Here, we show that intrinsic excitability of mouse dentate granule neurons exhibits a 24-h oscillation that controls spiking probability. Diurnal changes in excitability are mediated by antiphase G-protein regulation of potassium and sodium currents that reduce excitability during the Light phase. Disruption of the circadian transcrip-tional machinery by conditional deletion of Bmal1 enhances excitability selectively during the Light phase by removing G-protein regulation. These results reveal that circadian transcriptional machinery regulates intrinsic excitability by coordinated regulation of ion channels by G-protein signaling, highlighting a potential novel mechanism of cell-autonomous oscillations.
引用
收藏
页数:19
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