Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1783364379195998208 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6195348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT baduraaleksandra normalcognitiveandsocialdevelopmentrequireposteriorcerebellaractivity AT verpeutjessical normalcognitiveandsocialdevelopmentrequireposteriorcerebellaractivity AT metzgerjuliaw normalcognitiveandsocialdevelopmentrequireposteriorcerebellaractivity AT pereiratalmod normalcognitiveandsocialdevelopmentrequireposteriorcerebellaractivity AT pisanothomasj normalcognitiveandsocialdevelopmentrequireposteriorcerebellaractivity AT deverettben normalcognitiveandsocialdevelopmentrequireposteriorcerebellaractivity AT bakshinskayadariyae normalcognitiveandsocialdevelopmentrequireposteriorcerebellaractivity AT wangsamuelsh normalcognitiveandsocialdevelopmentrequireposteriorcerebellaractivity |