Loading…
Studying Cerebellar Circuits by Remote Control of Selected Neuronal Types with GABA(A) Receptors
Although GABA(A) receptor-mediated inhibition of cerebellar Purkinje cells by molecular layer interneurons (MLIs) has been studied intensely at the cellular level, it has remained unclear how this inhibition regulates cerebellum-dependent behaviour. We have implemented two complementary approaches t...
Saved in:
Published in: | Frontiers in molecular neuroscience 2009-01, Vol.2, p.29-29 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c367t-3198998a1423372425a2b4e6b080c0f3223830dd104eb444e94950fbf5744be53 |
---|---|
cites | |
container_end_page | 29 |
container_issue | |
container_start_page | 29 |
container_title | Frontiers in molecular neuroscience |
container_volume | 2 |
creator | Wisden, William Murray, Andrew J McClure, Christina Wulff, Peer |
description | Although GABA(A) receptor-mediated inhibition of cerebellar Purkinje cells by molecular layer interneurons (MLIs) has been studied intensely at the cellular level, it has remained unclear how this inhibition regulates cerebellum-dependent behaviour. We have implemented two complementary approaches to investigate the function of the MLI-Purkinje cell synapse on the behavioural level. In the first approach we permanently disrupted inhibitory fast synaptic transmission at the synapse by genetically removing the postsynaptic GABA(A) receptors from Purkinje cells (PC-Deltagamma2 mice). We found that chronic disruption of the MLI-Purkinje cell synapse strongly impaired cerebellar learning of the vestibular occular reflex (VOR), presumably by disrupting the temporal patterns of Purkinje cell activity. However, in PC-Deltagamma2 mice the baseline VOR reflex was only mildly affected; indeed PC-Deltagamma2 mice show no ataxia or gait abnormalities, suggesting that MLI control of Purkinje cell activity is either not involved in ongoing motor tasks or that the system compensates for its loss. To investigate the latter possibility we developed an alternative genetic technique; we made the MLI-Purkinje cell synapse selectively sensitive to rapid manipulation with the GABA(A) receptor modulator zolpidem (PC-gamma2-swap mice). Minutes after intraperitoneal zolpidem injection, these PC-gamma2-swap mice developed severe motor abnormalities, revealing a substantial contribution of the MLI-Purkinje cell synapses to real time motor control. The cell-type selective permanent knockout of synaptic GABAergic input and the fast reversible modulation of GABAergic input at the same synapse illustrate how pursuing both strategies gives a fuller view. |
doi_str_mv | 10.3389/neuro.02.029.2009 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_6197e0eba5484236bd2092c2dc989af0</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_6197e0eba5484236bd2092c2dc989af0</doaj_id><sourcerecordid>734237281</sourcerecordid><originalsourceid>FETCH-LOGICAL-c367t-3198998a1423372425a2b4e6b080c0f3223830dd104eb444e94950fbf5744be53</originalsourceid><addsrcrecordid>eNpdUduKFDEQbURxL_oBvkjAB_Vhxsqlk87j2LgXWFZw1-eYpKvXHno6Y5JG5u83s7MuslBQRXHOqeKcqnpHYcl5o79MOMewBFZKLxmAflEdUynZogatX_43H1UnKa0BJJM1f10dFaySSvLj6tdNnrvdMN2RFiM6HEcbSTtEPw85EbcjP3ATMpI2TDmGkYSe3OCIPmNHrvfnJzuS290WE_k75N_kfPV19Wn1udA8bnOI6U31qrdjwreP_bT6efbttr1YXH0_v2xXVwvPpcoLTnWjdWOpYJwrJlhtmRMoHTTgoeeM8YZD11EQ6IQQqIWuoXd9rYRwWPPT6vKg2wW7Nts4bGzcmWAH87AI8c7YmAc_opFUKwR0thZNOSddx0AzzzpffrA9FK2PB61tDH9mTNlshuT33kwY5mQULzTFGlqQH54h12GOxZNkGIem2C2YKih6QPkYUorYP_1HweyTNA9JGmCltNknWTjvH5Vnt8HuifEvOn4P44aXhw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2308265427</pqid></control><display><type>article</type><title>Studying Cerebellar Circuits by Remote Control of Selected Neuronal Types with GABA(A) Receptors</title><source>Open Access: PubMed Central</source><source>ProQuest - Publicly Available Content Database</source><creator>Wisden, William ; Murray, Andrew J ; McClure, Christina ; Wulff, Peer</creator><creatorcontrib>Wisden, William ; Murray, Andrew J ; McClure, Christina ; Wulff, Peer</creatorcontrib><description>Although GABA(A) receptor-mediated inhibition of cerebellar Purkinje cells by molecular layer interneurons (MLIs) has been studied intensely at the cellular level, it has remained unclear how this inhibition regulates cerebellum-dependent behaviour. We have implemented two complementary approaches to investigate the function of the MLI-Purkinje cell synapse on the behavioural level. In the first approach we permanently disrupted inhibitory fast synaptic transmission at the synapse by genetically removing the postsynaptic GABA(A) receptors from Purkinje cells (PC-Deltagamma2 mice). We found that chronic disruption of the MLI-Purkinje cell synapse strongly impaired cerebellar learning of the vestibular occular reflex (VOR), presumably by disrupting the temporal patterns of Purkinje cell activity. However, in PC-Deltagamma2 mice the baseline VOR reflex was only mildly affected; indeed PC-Deltagamma2 mice show no ataxia or gait abnormalities, suggesting that MLI control of Purkinje cell activity is either not involved in ongoing motor tasks or that the system compensates for its loss. To investigate the latter possibility we developed an alternative genetic technique; we made the MLI-Purkinje cell synapse selectively sensitive to rapid manipulation with the GABA(A) receptor modulator zolpidem (PC-gamma2-swap mice). Minutes after intraperitoneal zolpidem injection, these PC-gamma2-swap mice developed severe motor abnormalities, revealing a substantial contribution of the MLI-Purkinje cell synapses to real time motor control. The cell-type selective permanent knockout of synaptic GABAergic input and the fast reversible modulation of GABAergic input at the same synapse illustrate how pursuing both strategies gives a fuller view.</description><identifier>ISSN: 1662-5099</identifier><identifier>EISSN: 1662-5099</identifier><identifier>DOI: 10.3389/neuro.02.029.2009</identifier><identifier>PMID: 20076763</identifier><language>eng</language><publisher>Switzerland: Frontiers Research Foundation</publisher><subject>Ataxia ; Cerebellum ; Gait ; Interneurons ; Investigations ; memory consolidation ; Motor task performance ; Neurons ; Purkinje cell ; Purkinje cells ; Remote control ; Synaptic transmission ; Vestibular system ; Vestibulo-ocular reflex ; Zolpidem ; β-carboline ; γ-aminobutyric acid type A receptor ; γ-Aminobutyric acid A receptors</subject><ispartof>Frontiers in molecular neuroscience, 2009-01, Vol.2, p.29-29</ispartof><rights>2009. Notwithstanding the ProQuest Terms and conditions, you may use this content in accordance with the associated terms available at https://www.frontiersin.org/articles/10.3389/neuro.02.029.2009 .</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c367t-3198998a1423372425a2b4e6b080c0f3223830dd104eb444e94950fbf5744be53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2308265427/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2308265427?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25752,27923,27924,37011,37012,44589,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20076763$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wisden, William</creatorcontrib><creatorcontrib>Murray, Andrew J</creatorcontrib><creatorcontrib>McClure, Christina</creatorcontrib><creatorcontrib>Wulff, Peer</creatorcontrib><title>Studying Cerebellar Circuits by Remote Control of Selected Neuronal Types with GABA(A) Receptors</title><title>Frontiers in molecular neuroscience</title><addtitle>Front Mol Neurosci</addtitle><description>Although GABA(A) receptor-mediated inhibition of cerebellar Purkinje cells by molecular layer interneurons (MLIs) has been studied intensely at the cellular level, it has remained unclear how this inhibition regulates cerebellum-dependent behaviour. We have implemented two complementary approaches to investigate the function of the MLI-Purkinje cell synapse on the behavioural level. In the first approach we permanently disrupted inhibitory fast synaptic transmission at the synapse by genetically removing the postsynaptic GABA(A) receptors from Purkinje cells (PC-Deltagamma2 mice). We found that chronic disruption of the MLI-Purkinje cell synapse strongly impaired cerebellar learning of the vestibular occular reflex (VOR), presumably by disrupting the temporal patterns of Purkinje cell activity. However, in PC-Deltagamma2 mice the baseline VOR reflex was only mildly affected; indeed PC-Deltagamma2 mice show no ataxia or gait abnormalities, suggesting that MLI control of Purkinje cell activity is either not involved in ongoing motor tasks or that the system compensates for its loss. To investigate the latter possibility we developed an alternative genetic technique; we made the MLI-Purkinje cell synapse selectively sensitive to rapid manipulation with the GABA(A) receptor modulator zolpidem (PC-gamma2-swap mice). Minutes after intraperitoneal zolpidem injection, these PC-gamma2-swap mice developed severe motor abnormalities, revealing a substantial contribution of the MLI-Purkinje cell synapses to real time motor control. The cell-type selective permanent knockout of synaptic GABAergic input and the fast reversible modulation of GABAergic input at the same synapse illustrate how pursuing both strategies gives a fuller view.</description><subject>Ataxia</subject><subject>Cerebellum</subject><subject>Gait</subject><subject>Interneurons</subject><subject>Investigations</subject><subject>memory consolidation</subject><subject>Motor task performance</subject><subject>Neurons</subject><subject>Purkinje cell</subject><subject>Purkinje cells</subject><subject>Remote control</subject><subject>Synaptic transmission</subject><subject>Vestibular system</subject><subject>Vestibulo-ocular reflex</subject><subject>Zolpidem</subject><subject>β-carboline</subject><subject>γ-aminobutyric acid type A receptor</subject><subject>γ-Aminobutyric acid A receptors</subject><issn>1662-5099</issn><issn>1662-5099</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdUduKFDEQbURxL_oBvkjAB_Vhxsqlk87j2LgXWFZw1-eYpKvXHno6Y5JG5u83s7MuslBQRXHOqeKcqnpHYcl5o79MOMewBFZKLxmAflEdUynZogatX_43H1UnKa0BJJM1f10dFaySSvLj6tdNnrvdMN2RFiM6HEcbSTtEPw85EbcjP3ATMpI2TDmGkYSe3OCIPmNHrvfnJzuS290WE_k75N_kfPV19Wn1udA8bnOI6U31qrdjwreP_bT6efbttr1YXH0_v2xXVwvPpcoLTnWjdWOpYJwrJlhtmRMoHTTgoeeM8YZD11EQ6IQQqIWuoXd9rYRwWPPT6vKg2wW7Nts4bGzcmWAH87AI8c7YmAc_opFUKwR0thZNOSddx0AzzzpffrA9FK2PB61tDH9mTNlshuT33kwY5mQULzTFGlqQH54h12GOxZNkGIem2C2YKih6QPkYUorYP_1HweyTNA9JGmCltNknWTjvH5Vnt8HuifEvOn4P44aXhw</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Wisden, William</creator><creator>Murray, Andrew J</creator><creator>McClure, Christina</creator><creator>Wulff, Peer</creator><general>Frontiers Research Foundation</general><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7XB</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>20090101</creationdate><title>Studying Cerebellar Circuits by Remote Control of Selected Neuronal Types with GABA(A) Receptors</title><author>Wisden, William ; Murray, Andrew J ; McClure, Christina ; Wulff, Peer</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c367t-3198998a1423372425a2b4e6b080c0f3223830dd104eb444e94950fbf5744be53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Ataxia</topic><topic>Cerebellum</topic><topic>Gait</topic><topic>Interneurons</topic><topic>Investigations</topic><topic>memory consolidation</topic><topic>Motor task performance</topic><topic>Neurons</topic><topic>Purkinje cell</topic><topic>Purkinje cells</topic><topic>Remote control</topic><topic>Synaptic transmission</topic><topic>Vestibular system</topic><topic>Vestibulo-ocular reflex</topic><topic>Zolpidem</topic><topic>β-carboline</topic><topic>γ-aminobutyric acid type A receptor</topic><topic>γ-Aminobutyric acid A receptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wisden, William</creatorcontrib><creatorcontrib>Murray, Andrew J</creatorcontrib><creatorcontrib>McClure, Christina</creatorcontrib><creatorcontrib>Wulff, Peer</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest - Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in molecular neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wisden, William</au><au>Murray, Andrew J</au><au>McClure, Christina</au><au>Wulff, Peer</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Studying Cerebellar Circuits by Remote Control of Selected Neuronal Types with GABA(A) Receptors</atitle><jtitle>Frontiers in molecular neuroscience</jtitle><addtitle>Front Mol Neurosci</addtitle><date>2009-01-01</date><risdate>2009</risdate><volume>2</volume><spage>29</spage><epage>29</epage><pages>29-29</pages><issn>1662-5099</issn><eissn>1662-5099</eissn><abstract>Although GABA(A) receptor-mediated inhibition of cerebellar Purkinje cells by molecular layer interneurons (MLIs) has been studied intensely at the cellular level, it has remained unclear how this inhibition regulates cerebellum-dependent behaviour. We have implemented two complementary approaches to investigate the function of the MLI-Purkinje cell synapse on the behavioural level. In the first approach we permanently disrupted inhibitory fast synaptic transmission at the synapse by genetically removing the postsynaptic GABA(A) receptors from Purkinje cells (PC-Deltagamma2 mice). We found that chronic disruption of the MLI-Purkinje cell synapse strongly impaired cerebellar learning of the vestibular occular reflex (VOR), presumably by disrupting the temporal patterns of Purkinje cell activity. However, in PC-Deltagamma2 mice the baseline VOR reflex was only mildly affected; indeed PC-Deltagamma2 mice show no ataxia or gait abnormalities, suggesting that MLI control of Purkinje cell activity is either not involved in ongoing motor tasks or that the system compensates for its loss. To investigate the latter possibility we developed an alternative genetic technique; we made the MLI-Purkinje cell synapse selectively sensitive to rapid manipulation with the GABA(A) receptor modulator zolpidem (PC-gamma2-swap mice). Minutes after intraperitoneal zolpidem injection, these PC-gamma2-swap mice developed severe motor abnormalities, revealing a substantial contribution of the MLI-Purkinje cell synapses to real time motor control. The cell-type selective permanent knockout of synaptic GABAergic input and the fast reversible modulation of GABAergic input at the same synapse illustrate how pursuing both strategies gives a fuller view.</abstract><cop>Switzerland</cop><pub>Frontiers Research Foundation</pub><pmid>20076763</pmid><doi>10.3389/neuro.02.029.2009</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1662-5099 |
ispartof | Frontiers in molecular neuroscience, 2009-01, Vol.2, p.29-29 |
issn | 1662-5099 1662-5099 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_6197e0eba5484236bd2092c2dc989af0 |
source | Open Access: PubMed Central; ProQuest - Publicly Available Content Database |
subjects | Ataxia Cerebellum Gait Interneurons Investigations memory consolidation Motor task performance Neurons Purkinje cell Purkinje cells Remote control Synaptic transmission Vestibular system Vestibulo-ocular reflex Zolpidem β-carboline γ-aminobutyric acid type A receptor γ-Aminobutyric acid A receptors |
title | Studying Cerebellar Circuits by Remote Control of Selected Neuronal Types with GABA(A) Receptors |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T08%3A29%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Studying%20Cerebellar%20Circuits%20by%20Remote%20Control%20of%20Selected%20Neuronal%20Types%20with%20GABA(A)%20Receptors&rft.jtitle=Frontiers%20in%20molecular%20neuroscience&rft.au=Wisden,%20William&rft.date=2009-01-01&rft.volume=2&rft.spage=29&rft.epage=29&rft.pages=29-29&rft.issn=1662-5099&rft.eissn=1662-5099&rft_id=info:doi/10.3389/neuro.02.029.2009&rft_dat=%3Cproquest_doaj_%3E734237281%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c367t-3198998a1423372425a2b4e6b080c0f3223830dd104eb444e94950fbf5744be53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2308265427&rft_id=info:pmid/20076763&rfr_iscdi=true |