CPT1C is required for synaptic plasticity and oscillatory activity that supports motor, associative and non‐associative learning

Carnitine palmitoyltransferase 1c (CPT1C) is a neuron‐specific protein widely distributed throughout the CNS and highly expressed in discrete brain areas including the hypothalamus, hippocampus, amygdala and different motor regions. Its deficiency has recently been shown to disrupt dendritic spine m...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of physiology Vol. 601; no. 16; pp. 3533 - 3556
Main Authors: Iborra‐Lázaro, Guillermo, Djebari, Souhail, Sánchez‐Rodríguez, Irene, Gratacòs‐Batlle, Esther, Sánchez‐Fernández, Nuria, Radošević, Marija, Casals, Núria, Navarro‐López, Juan de Dios, Soto del Cerro, David, Jiménez‐Díaz, Lydia
Format: Journal Article
Language:English
Published: England Wiley Subscription Services, Inc 01-08-2023
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Carnitine palmitoyltransferase 1c (CPT1C) is a neuron‐specific protein widely distributed throughout the CNS and highly expressed in discrete brain areas including the hypothalamus, hippocampus, amygdala and different motor regions. Its deficiency has recently been shown to disrupt dendritic spine maturation and AMPA receptor synthesis and trafficking in the hippocampus, but its contribution to synaptic plasticity and cognitive learning and memory processes remains mostly unknown. Here, we aimed to explore the molecular, synaptic, neural network and behavioural role of CPT1C in cognition‐related functions by using CPT1C knockout (KO) mice. CPT1C‐deficient mice showed extensive learning and memory deficits. The CPT1C KO animals exhibited impaired motor and instrumental learning that seemed to be related, in part, to locomotor deficits and muscle weakness but not to mood alterations. In addition, CPT1C KO mice showed detrimental hippocampus‐dependent spatial and habituation memory, most probably attributable to inefficient dendritic spine maturation, impairments in long‐term plasticity at the CA3–CA1 synapse and aberrant cortical oscillatory activity. In conclusion, our results reveal that CPT1C is not only crucial for motor function, coordination and energy homeostasis, but also has a crucial role in the maintenance of learning and memory cognitive functions. Key points CPT1C, a neuron‐specific interactor protein involved in AMPA receptor synthesis and trafficking, was found to be highly expressed in the hippocampus, amygdala and various motor regions. CPT1C‐deficient animals exhibited energy deficits and impaired locomotion, but no mood changes were found. CPT1C deficiency disrupts hippocampal dendritic spine maturation and long‐term synaptic plasticity and reduces cortical γ oscillations. CPT1C was found to be crucial for motor, associative and non‐associative learning and memory. figure legend CPT1C regulates the trafficking of AMPA receptors containing the GluA1 subunit to the membrane surface and the maturation of dendritic spines in the hippocampus. The absence of CPT1C compromises hippocampal synaptic plasticity and cortical oscillatory processes, causes motor and energy dysfunction and induces cognitive deficits affecting associative and non‐associative forms of learning and memory.
Bibliography:The peer review history is available in the Supporting information section of this article
J. de D. Navarro‐López, D. S. del Cerro and L. Jiménez‐Díaz contributed equally to this work and they share last authorship.
https://doi.org/10.1113/JP284248#support‐information‐section
Handling Editors: David Wyllie & James Coxon
.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0022-3751
1469-7793
DOI:10.1113/JP284248