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Intrinsic Cell-Class-Specific Modulation of Intracellular Chloride Levels and Inhibitory Function, in Cortical Networks, between Day and Night

Lookup NU author(s): Dr Laura Alberio, Amy Marshall, Dr Rob Graham, Connie Mackenzie-Gray Scott, Dr Luciano Saieva, Dr Sasha Gartside, Professor Andrew Trevelyan

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

Copyright © 2025 Alberio et al. Recent work showed unexpectedly large, daily modulation of intracellular chloride concentration ([Cl-]in) in cortical pyramidal cells, with consequences for GABAergic function and network excitability ( Alfonsa et al., 2023; Pracucci et al., 2023). One explanation for this [Cl-]in modulation is that it arises from variation in presynaptic drive. In that case, neuronal classes with similar synaptic inputs should show correlated changes in activity-dependent ionic redistribution. To examine this prediction, we performed in vivo, LSSm-ClopHensor imaging to measure [Cl-]in and pHin in populations of parvalbumin- (PV) and somatostatin (SST)-expressing interneurons in neocortical Layer 2/3 of male and female adult mice. Imaging was performed at zeitgeber time (ZT)5 and ZT17, when pyramidal cell [Cl-]in shows maximal divergence ( Pracucci et al., 2023). Interestingly, PV interneurons also showed large physiological [Cl-]in modulation between these times but out-of-phase with that in pyramidal cells, being raised at ZT5 and lower at ZT17, and with a far higher mean [Cl-]in SST interneurons showed less modulation, with higher variance, and with a temporal dynamic resembling the pyramidal cell pattern. Notably, in vitro experimental assays of inhibition, involving these two classes of interneuron, differed markedly at ZT5 and ZT17. The persistence of these time-of-day effects in vitro and the difference in [Cl-]in dynamics between pyramidal cells and PV interneurons in vivo both point toward cell-intrinsic regulation being more important than activity-dependent effects in setting these slow, daily, physiological, ionic redistribution patterns. We discuss what other possible factors may influence variations in brain state through the day.


Publication metadata

Author(s): Alberio L, Marshall A, Graham RT, MacKenzie-Gray Scott C, Saieva L, Gartside SE, Ratto GM, Trevelyan AJ

Publication type: Article

Publication status: Published

Journal: eNeuro

Year: 2025

Volume: 12

Issue: 12

Online publication date: 02/12/2025

Acceptance date: 10/10/2025

Date deposited: 12/01/2026

ISSN (electronic): 2373-2822

Publisher: Society for Neuroscience

URL: https://doi.org/10.1523/ENEURO.0325-25.2025

DOI: 10.1523/ENEURO.0325-25.2025

PubMed id: 41330631


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Funding

Funder referenceFunder name
#NEXTGENERATIONEU (NGEU)
BB/P019854/1Biotechnology and Biological Sciences Research Council (BBSRC)
Epilepsy Research Institute Doctoral Training Programme
Epilepsy Research UK (Celine Newman Bursary)
Ministry of University and Research (MUR)
MR/R005427/1Medical Research Council (MRC)
National Recovery and Resilience Plan (NRRP)
Newcastle University Faculty Fellowship
Newcastle University Faculty PhD studentship
Regione Toscana project DECODE-EE
Project MNESYS (PE0000006)
Royal Society/CNR grant

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