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Publication : GSK3 activity regulates rhythms in hippocampal clock gene expression and synaptic plasticity.

First Author  Besing RC Year  2017
Journal  Hippocampus Volume  27
Issue  8 Pages  890-898
PubMed ID  28556462 Mgi Jnum  J:273508
Mgi Id  MGI:6294161 Doi  10.1002/hipo.22739
Citation  Besing RC, et al. (2017) GSK3 activity regulates rhythms in hippocampal clock gene expression and synaptic plasticity. Hippocampus 27(8):890-898
abstractText  Hippocampal rhythms in clock gene expression, enzymatic activity, and long-term potentiation (LTP) are thought to underlie day-night differences in memory acquisition and recall. Glycogen synthase kinase 3-beta (GSK3beta) is a known regulator of hippocampal function, and inhibitory phosphorylation of GSK3beta exhibits region-specific differences over the light-dark cycle. Here, we sought to determine whether phosphorylation of both GSK3alpha and GSK3beta isoforms has an endogenous circadian rhythm in specific areas of the hippocampus and whether chronic inhibition or activation alters the molecular clock and hippocampal plasticity (LTP). Results indicated a significant endogenous circadian rhythm in phosphorylation of GSK3beta, but not GSK3alpha, in hippocampal CA1 extracts from mice housed in constant darkness for at least 2 weeks. To examine the importance of this rhythm, genetic and pharmacological strategies were used to disrupt the GSK3 activity rhythm by chronically activating or inhibiting GSK3. Chronic activation of both GSK3 isoforms in transgenic mice (GSK3-KI mice) diminished rhythmic BMAL1 expression. On the other hand, chronic treatment with a GSK3 inhibitor significantly shortened the molecular clock period of organotypic hippocampal PER2::LUC cultures. While WT mice exhibited higher LTP magnitude at night compared to day, the day-night difference in LTP magnitude remained with greater magnitude at both times of day in mice with chronic GSK3 activity. On the other hand, pharmacological GSK3 inhibition impaired day-night differences in LTP by blocking LTP selectively at night. Taken together, these results support the model that circadian rhythmicity of hippocampal GSK3beta activation state regulates day/night differences in molecular clock periodicity and a major form of synaptic plasticity (LTP).
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