Abstract
SUMMARYIn various mental disorders, dysfunction of the prefrontal cortex contributes to cognitive deficits. Here we studied how the claustrum (CLA), a nucleus sharing reciprocal connections with the cortex, may participate in these cognitive impairments. We show that specific ensembles of CLA and of medial prefrontal cortex (mPFC) neurons are activated during a task requiring cognitive control such as attentional set-shifting, i.e. the ability to shift attention towards newly relevant stimulus-reward associations while disengaging from irrelevant ones. CLA neurons exert a direct excitatory input on mPFC pyramidal cells, and chemogenetic inhibition of CLA neurons suppresses the formation of specific mPFC assemblies during attentional set-shifting. Furthermore, impairing the recruitment of specific CLA assemblies through opto/chemogenetic manipulations prevents attentional set-shifting. In conclusion, we propose that the CLA controls the reorganization of mPFC ensembles to enable attentional set-shifting, emphasizing a potential role of the CLA-mPFC network in attentional dysfunctions.
Publisher
Cold Spring Harbor Laboratory
Reference106 articles.
1. A whole-brain atlas of monosynaptic input targeting four different cell types in the medial prefrontal cortex of the mouse
2. Remote Control of Neuronal Activity in Transgenic Mice Expressing Evolved G Protein-Coupled Receptors
3. Andrews, T.S. , and Hemberg, M. (2018). M3Drop: Dropout-based feature selection for scRNASeq. Bioinformatics.
4. Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand
5. Arya, S. , Mount, D. , Netanyahu, N. , Silverman, R. , and Wu, A. (1998). An Optimal Algorithm for Approximate Nearest Neighbor Searching Fixed Dimensions, Vol 45.
Cited by
23 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献