TRPC3 is a major contributor to functional heterogeneity of cerebellar Purkinje cells

Author:

Wu Bin1ORCID,Blot François GC1,Wong Aaron Benson1ORCID,Osório Catarina1,Adolfs Youri2,Pasterkamp R Jeroen2ORCID,Hartmann Jana3,Becker Esther BE4ORCID,Boele Henk-Jan1,De Zeeuw Chris I15ORCID,Schonewille Martijn1ORCID

Affiliation:

1. Department of Neuroscience, Erasmus Medical Center, Rotterdam, Netherlands

2. Department of Translational Neuroscience, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands

3. Institute of Neuroscience, Technical University Munich, Munich, Germany

4. Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom

5. Netherlands Institute for Neuroscience, Royal Dutch Academy for Arts and Sciences, Amsterdam, Netherlands

Abstract

Despite the canonical homogeneous character of its organization, the cerebellum plays differential computational roles in distinct sensorimotor behaviors. Previously, we showed that Purkinje cell (PC) activity differs between zebrin-negative (Z–) and zebrin-positive (Z+) modules (Zhou et al., 2014). Here, using gain-of-function and loss-of-function mouse models, we show that transient receptor potential cation channel C3 (TRPC3) controls the simple spike activity of Z–, but not Z+ PCs. In addition, TRPC3 regulates complex spike rate and their interaction with simple spikes, exclusively in Z– PCs. At the behavioral level, TRPC3 loss-of-function mice show impaired eyeblink conditioning, which is related to Z– modules, whereas compensatory eye movement adaptation, linked to Z+ modules, is intact. Together, our results indicate that TRPC3 is a major contributor to the cellular heterogeneity that introduces distinct physiological properties in PCs, conjuring functional heterogeneity in cerebellar sensorimotor integration.

Funder

European Commission

China Scholarship Council

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

Center for Integrated Protein Science Munich

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference74 articles.

1. Speech deficits in ischaemic cerebellar lesions;Ackermann;Journal of Neurology,1992

2. The cloning of zebrin II reveals its identity with aldolase C;Ahn;Development,1994

3. Locomotor activity modulates associative learning in mouse cerebellum;Albergaria;Nature Neuroscience,2018

4. Cellular heterogeneity: do differences make a difference?;Altschuler;Cell,2010

5. Cerebellar modules and their role as operational cerebellar processing units;Apps;The Cerebellum,2018

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3