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Normal cognitive and social development require posterior cerebellar activity

Cognitive and social capacities require postnatal experience, yet the pathways by which experience guides development are unknown. Here we show that the normal development of motor and nonmotor capacities requires cerebellar activity. Using chemogenetic perturbation of molecular layer interneurons t...

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Autores principales: Badura, Aleksandra, Verpeut, Jessica L, Metzger, Julia W, Pereira, Talmo D, Pisano, Thomas J, Deverett, Ben, Bakshinskaya, Dariya E, Wang, Samuel S-H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6195348/
https://www.ncbi.nlm.nih.gov/pubmed/30226467
http://dx.doi.org/10.7554/eLife.36401
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author Badura, Aleksandra
Verpeut, Jessica L
Metzger, Julia W
Pereira, Talmo D
Pisano, Thomas J
Deverett, Ben
Bakshinskaya, Dariya E
Wang, Samuel S-H
author_facet Badura, Aleksandra
Verpeut, Jessica L
Metzger, Julia W
Pereira, Talmo D
Pisano, Thomas J
Deverett, Ben
Bakshinskaya, Dariya E
Wang, Samuel S-H
author_sort Badura, Aleksandra
collection PubMed
description Cognitive and social capacities require postnatal experience, yet the pathways by which experience guides development are unknown. Here we show that the normal development of motor and nonmotor capacities requires cerebellar activity. Using chemogenetic perturbation of molecular layer interneurons to attenuate cerebellar output in mice, we found that activity of posterior regions in juvenile life modulates adult expression of eyeblink conditioning (paravermal lobule VI, crus I), reversal learning (lobule VI), persistive behavior and novelty-seeking (lobule VII), and social preference (crus I/II). Perturbation in adult life altered only a subset of phenotypes. Both adult and juvenile disruption left gait metrics largely unaffected. Contributions to phenotypes increased with the amount of lobule inactivated. Using an anterograde transsynaptic tracer, we found that posterior cerebellum made strong connections with prelimbic, orbitofrontal, and anterior cingulate cortex. These findings provide anatomical substrates for the clinical observation that cerebellar injury increases the risk of autism.
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spelling pubmed-61953482018-10-22 Normal cognitive and social development require posterior cerebellar activity Badura, Aleksandra Verpeut, Jessica L Metzger, Julia W Pereira, Talmo D Pisano, Thomas J Deverett, Ben Bakshinskaya, Dariya E Wang, Samuel S-H eLife Neuroscience Cognitive and social capacities require postnatal experience, yet the pathways by which experience guides development are unknown. Here we show that the normal development of motor and nonmotor capacities requires cerebellar activity. Using chemogenetic perturbation of molecular layer interneurons to attenuate cerebellar output in mice, we found that activity of posterior regions in juvenile life modulates adult expression of eyeblink conditioning (paravermal lobule VI, crus I), reversal learning (lobule VI), persistive behavior and novelty-seeking (lobule VII), and social preference (crus I/II). Perturbation in adult life altered only a subset of phenotypes. Both adult and juvenile disruption left gait metrics largely unaffected. Contributions to phenotypes increased with the amount of lobule inactivated. Using an anterograde transsynaptic tracer, we found that posterior cerebellum made strong connections with prelimbic, orbitofrontal, and anterior cingulate cortex. These findings provide anatomical substrates for the clinical observation that cerebellar injury increases the risk of autism. eLife Sciences Publications, Ltd 2018-09-20 /pmc/articles/PMC6195348/ /pubmed/30226467 http://dx.doi.org/10.7554/eLife.36401 Text en © 2018, Badura et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Badura, Aleksandra
Verpeut, Jessica L
Metzger, Julia W
Pereira, Talmo D
Pisano, Thomas J
Deverett, Ben
Bakshinskaya, Dariya E
Wang, Samuel S-H
Normal cognitive and social development require posterior cerebellar activity
title Normal cognitive and social development require posterior cerebellar activity
title_full Normal cognitive and social development require posterior cerebellar activity
title_fullStr Normal cognitive and social development require posterior cerebellar activity
title_full_unstemmed Normal cognitive and social development require posterior cerebellar activity
title_short Normal cognitive and social development require posterior cerebellar activity
title_sort normal cognitive and social development require posterior cerebellar activity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6195348/
https://www.ncbi.nlm.nih.gov/pubmed/30226467
http://dx.doi.org/10.7554/eLife.36401
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