Abstract

Social recognition memory (SRM) is a key determinant of social interactions. While the cerebellum emerges as an important region for social behavior, how cerebellar activity affects social functions remains unclear. We selectively increased the excitability of molecular layer interneurons (MLIs) to suppress Purkinje cell firing in the mouse cerebellar vermis. Chemogenetic perturbation of MLIs impaired SRM without affecting sociability, anxiety levels, motor coordination or object recognition. Optogenetic interference of MLIs during distinct phases of a social recognition test revealed the cerebellar engagement in the retrieval, but not encoding, of social information. c-Fos mapping after the social recognition test showed that cerebellar manipulation decreased brain-wide interregional correlations and altered network structure from medial prefrontal cortex and hippocampus-centered to amygdala-centered modules. Anatomical tracing demonstrated hierarchical projections from the central cerebellum to the social brain network integrating amygdalar connections. Our findings suggest that the cerebellum organizes the neural matrix necessary for SRM.

Social memory integrates past experiences into social interactions by distinguishing familiar from novel conspecifics. In this study, the authors delineated a role of the cerebellum in organizing the neural matrix required for social memory.

Details

Title
Social memory deficit caused by dysregulation of the cerebellar vermis
Author
Chao, Owen Y. 1 ; Pathak, Salil Saurav 1 ; Zhang, Hao 1   VIAFID ORCID Logo  ; Augustine, George J. 2   VIAFID ORCID Logo  ; Christie, Jason M. 3 ; Kikuchi, Chikako 4 ; Taniguchi, Hiroki 5 ; Yang, Yi-Mei 6   VIAFID ORCID Logo 

 Department of Biomedical Sciences, University of Minnesota Medical School, Duluth, USA (GRID:grid.17635.36) (ISNI:0000000419368657) 
 Nanyang Technological University, Lee Kong Chian School of Medicine, Singapore, Singapore (GRID:grid.59025.3b) (ISNI:0000 0001 2224 0361) 
 University of Colorado School of Medicine, Aurora, USA (GRID:grid.430503.1) (ISNI:0000 0001 0703 675X) 
 Max Planck Florida Institute for Neuroscience, Jupiter, USA (GRID:grid.421185.b) (ISNI:0000 0004 0380 459X) 
 Department of Pathology, Ohio State University Wexner Medical Center, Columbus, USA (GRID:grid.412332.5) (ISNI:0000 0001 1545 0811); Chronic Brain Injury, Ohio State University Wexner Medical Center, Columbus, USA (GRID:grid.412332.5) (ISNI:0000 0001 1545 0811) 
 Department of Biomedical Sciences, University of Minnesota Medical School, Duluth, USA (GRID:grid.17635.36) (ISNI:0000000419368657); Department of Neuroscience, University of Minnesota, Minneapolis, USA (GRID:grid.17635.36) (ISNI:0000 0004 1936 8657) 
Pages
6007
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2869052271
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.