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Transient juvenile demyelination impairs maturation and function of parvalbumin-positive interneurons in the prefrontal cortex

Abstract:
Recent studies have highlighted axonal myelination as a common feature of parvalbumin-positive (PV) interneurons throughout the cerebral cortex. However, the precise function of PV interneuron myelination remains incompletely understood. In this study, we used the cuprizone model of demyelination in mice to investigate how PV interneuron myelination might influence their neuronal physiology. Specifically, we examined whether impairing myelination from postnatal day 21 onwards, during a critical neurodevelopmental period of the prefrontal cortex (PFC), can affect PV interneuron maturation and function. Using whole-cell patch-clamp recordings to examine intrinsic properties of PV interneurons in the PFC, we found that juvenile demyelination in mice induced robust alterations of PV interneuron firing patterns. Specifically, we observed that demyelination caused an impairment in the ability of PV interneurons to sustain high-frequency firing associated with a substantial decrease in Kv3-specific currents. We also found a significant impairment in PV interneuron autaptic self-inhibitory transmission, a feature implicated in temporal control of PV interneuron firing during cortical network activity. Following a remyelination period of 5 weeks, PV interneuron properties were only partially recovered, suggesting that transient juvenile demyelination leads to long-lasting impairments of PV interneuron function. In contrast, adult demyelination had no significant effects on PV interneuron firing properties. Together, our data uncovers a critical period for juvenile myelination as an important factor in PFC PV interneuron development and brain maturation.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1371/journal.pbio.3003421

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
Pharmacology
Sub department:
Pharmacology
Role:
Author
ORCID:
0000-0002-1754-283X
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Role:
Author
ORCID:
0000-0002-9777-3338


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Funder identifier:
https://ror.org/04jsz6e67
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Funder identifier:
https://ror.org/052gg0110
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Funder identifier:
https://ror.org/001aqnf71


Publisher:
Public Library of Science
Journal:
PLoS Biology More from this journal
Volume:
23
Issue:
9
Pages:
e3003421-e3003421
Article number:
e3003421
Publication date:
2025-09-30
Acceptance date:
2025-09-16
DOI:
EISSN:
1545-7885
ISSN:
1544-9173


Language:
English
Pubs id:
2300950
UUID:
uuid_696ee71f-8129-4a79-9a89-119b8dcdf7a9
Local pid:
pubs:2300950
Source identifiers:
3358611
Deposit date:
2025-10-09
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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