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Molecular and cellular rhythms in excitatory and inhibitory neurons in the mouse prefrontal cortex.

Jennifer N BurnsAaron K JenkinsRuoFei YinWei ZongChelsea A VadnieLauren M DePoyKaitlyn A PetersenMariya TsyglakovaMadeline R ScottGeorge C TsengYanhua H HuangColleen A McClung
Published in: bioRxiv : the preprint server for biology (2024)
Previous studies have shown that there are rhythms in gene expression in the mouse prefrontal cortex (PFC); however, the contribution of different cell types and potential variation by sex has not yet been determined. Of particular interest are excitatory pyramidal cells and inhibitory parvalbumin (PV) interneurons, as interactions between these cell types are essential for regulating the excitation/inhibition balance and controlling many of the cognitive functions regulated by the PFC. In this study, we identify cell-type specific rhythms in the translatome of PV and pyramidal cells in the mouse PFC and assess diurnal rhythms in PV cell electrophysiological properties. We find that while core molecular clock genes are conserved and synchronized between cell types, pyramidal cells have nearly twice as many rhythmic transcripts as PV cells (35% vs. 18%). Rhythmic transcripts in pyramidal cells also show a high degree of overlap between sexes, both in terms of which transcripts are rhythmic and in the biological processes associated with them. Conversely, in PV cells, rhythmic transcripts from males and females are largely distinct. Moreover, we find sex-specific effects of phase on action potential properties in PV cells that are eliminated by environmental circadian disruption. Together, this study demonstrates that rhythms in gene expression and electrophysiological properties in the mouse PFC vary by both cell type and sex. Moreover, the biological processes associated with these rhythmic transcripts may provide insight into the unique functions of rhythms in these cells, as well as their selective vulnerabilities to circadian disruption.
Keyphrases
  • induced apoptosis
  • gene expression
  • cell cycle arrest
  • signaling pathway
  • dna methylation
  • oxidative stress
  • prefrontal cortex
  • genome wide
  • bone marrow
  • human health