Pan-retinal characterisation of Light Responses from Ganglion Cells in the Developing Mouse Retina
We have investigated the ontogeny of light-driven responses in mouse retinal ganglion cells (RGCs). Using a large-scale, high-density multielectrode array, we recorded from hundreds to thousands of RGCs simultaneously at pan-retinal level, including dorsal and ventral locations. Responses to differe...
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description | We have investigated the ontogeny of light-driven responses in mouse retinal ganglion cells (RGCs). Using a large-scale, high-density multielectrode array, we recorded from hundreds to thousands of RGCs simultaneously at pan-retinal level, including dorsal and ventral locations. Responses to different contrasts not only revealed a complex developmental profile for ON, OFF and ON-OFF responses, but also unveiled differences between dorsal and ventral RGC responses. At eye-opening, dorsal RGCs of all types were more responsive to light, perhaps indicating an environmental priority to nest viewing for pre-weaning pups. The developmental profile of ON and OFF responses exhibited antagonistic behaviour, with the strongest ON responses shortly after eye-opening, followed by an increase in the strength of OFF responses later on. Further, we found that with maturation receptive field (RF) center sizes decrease, spike-triggered averaged responses to white noise become stronger, and centers become more circular while maintaining differences between RGC types. We conclude that the maturation of retinal functionality is not spatially homogeneous, likely reflecting ecological requirements that favour earlier maturation of the dorsal retina. |
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Using a large-scale, high-density multielectrode array, we recorded from hundreds to thousands of RGCs simultaneously at pan-retinal level, including dorsal and ventral locations. Responses to different contrasts not only revealed a complex developmental profile for ON, OFF and ON-OFF responses, but also unveiled differences between dorsal and ventral RGC responses. At eye-opening, dorsal RGCs of all types were more responsive to light, perhaps indicating an environmental priority to nest viewing for pre-weaning pups. The developmental profile of ON and OFF responses exhibited antagonistic behaviour, with the strongest ON responses shortly after eye-opening, followed by an increase in the strength of OFF responses later on. Further, we found that with maturation receptive field (RF) center sizes decrease, spike-triggered averaged responses to white noise become stronger, and centers become more circular while maintaining differences between RGC types. We conclude that the maturation of retinal functionality is not spatially homogeneous, likely reflecting ecological requirements that favour earlier maturation of the dorsal retina.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep42330</identifier><identifier>PMID: 28186129</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/378/2571/1696 ; 631/378/3917 ; 64/60 ; 9/10 ; 9/30 ; Action Potentials - radiation effects ; Aging - physiology ; Animals ; Electrodes ; Eye ; Humanities and Social Sciences ; Life Sciences ; Mice, Inbred C57BL ; multidisciplinary ; Neurons and Cognition ; Ontogeny ; Receptive field ; Retina ; Retinal ganglion cells ; Retinal Ganglion Cells - cytology ; Retinal Ganglion Cells - physiology ; Retinal Ganglion Cells - radiation effects ; Rodents ; Science ; Time Factors ; Weaning</subject><ispartof>Scientific reports, 2017-02, Vol.7 (1), p.42330-42330, Article 42330</ispartof><rights>The Author(s) 2017</rights><rights>Copyright Nature Publishing Group Feb 2017</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright © 2017, The Author(s) 2017 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c472t-d4531afc343ead5c8c632976a009730f3d953e17877ec65a69b49472287183223</citedby><cites>FETCH-LOGICAL-c472t-d4531afc343ead5c8c632976a009730f3d953e17877ec65a69b49472287183223</cites><orcidid>0000-0003-4906-1368 ; 0000-0003-1523-4187</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301206/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301206/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28186129$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://inria.hal.science/hal-01589946$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Hilgen, Gerrit</creatorcontrib><creatorcontrib>Pirmoradian, Sahar</creatorcontrib><creatorcontrib>Pamplona, Daniela</creatorcontrib><creatorcontrib>Kornprobst, Pierre</creatorcontrib><creatorcontrib>Cessac, Bruno</creatorcontrib><creatorcontrib>Hennig, Matthias H.</creatorcontrib><creatorcontrib>Sernagor, Evelyne</creatorcontrib><title>Pan-retinal characterisation of Light Responses from Ganglion Cells in the Developing Mouse Retina</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>We have investigated the ontogeny of light-driven responses in mouse retinal ganglion cells (RGCs). Using a large-scale, high-density multielectrode array, we recorded from hundreds to thousands of RGCs simultaneously at pan-retinal level, including dorsal and ventral locations. Responses to different contrasts not only revealed a complex developmental profile for ON, OFF and ON-OFF responses, but also unveiled differences between dorsal and ventral RGC responses. At eye-opening, dorsal RGCs of all types were more responsive to light, perhaps indicating an environmental priority to nest viewing for pre-weaning pups. The developmental profile of ON and OFF responses exhibited antagonistic behaviour, with the strongest ON responses shortly after eye-opening, followed by an increase in the strength of OFF responses later on. Further, we found that with maturation receptive field (RF) center sizes decrease, spike-triggered averaged responses to white noise become stronger, and centers become more circular while maintaining differences between RGC types. We conclude that the maturation of retinal functionality is not spatially homogeneous, likely reflecting ecological requirements that favour earlier maturation of the dorsal retina.</description><subject>631/378/2571/1696</subject><subject>631/378/3917</subject><subject>64/60</subject><subject>9/10</subject><subject>9/30</subject><subject>Action Potentials - radiation effects</subject><subject>Aging - physiology</subject><subject>Animals</subject><subject>Electrodes</subject><subject>Eye</subject><subject>Humanities and Social Sciences</subject><subject>Life Sciences</subject><subject>Mice, Inbred C57BL</subject><subject>multidisciplinary</subject><subject>Neurons and Cognition</subject><subject>Ontogeny</subject><subject>Receptive field</subject><subject>Retina</subject><subject>Retinal ganglion cells</subject><subject>Retinal Ganglion Cells - cytology</subject><subject>Retinal Ganglion Cells - physiology</subject><subject>Retinal Ganglion Cells - radiation effects</subject><subject>Rodents</subject><subject>Science</subject><subject>Time Factors</subject><subject>Weaning</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNplkd9rFDEQx4MottQ--A9IwBcrbM3PzeZFKKe2hSuK6HPI5WZ3U_aSNdk78L83y9XzbPOSMPOZ72Tmi9BrSi4p4c2HnGAUjHPyDJ0yImTFOGPPj94n6Dzne1KOZFpQ_RKdsIY2NWX6FK2-2VAlmHywA3a9TdZNkHy2k48BxxYvfddP-DvkMYYMGbcpbvC1Dd0wAwsYhox9wFMP-BPsYIijDx2-i9sMpWrWfYVetHbIcP5wn6GfXz7_WNxUy6_Xt4urZeWEYlO1FpJT2zouONi1dI2rOdOqtoRoxUnL11pyoKpRClwtba1XQpdK1ijalDH5Gfq41x23qw2sHYQp2cGMyW9s-m2i9eb_TPC96eLOSE4oI3URuNgL9I_Kbq6WZo4RKhutRb2jhX330CzFX1vIk9n47Mo2bIAyuyn7VVLUSs2ybx-h93Gbyr4LpQlVjAom_zV3KebiaXv4ASVmNtocjC7sm-NJD-RfWwvwfg_kkgodpKOWT9T-AKNzsGY</recordid><startdate>20170210</startdate><enddate>20170210</enddate><creator>Hilgen, Gerrit</creator><creator>Pirmoradian, Sahar</creator><creator>Pamplona, Daniela</creator><creator>Kornprobst, Pierre</creator><creator>Cessac, Bruno</creator><creator>Hennig, Matthias H.</creator><creator>Sernagor, Evelyne</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</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>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4906-1368</orcidid><orcidid>https://orcid.org/0000-0003-1523-4187</orcidid></search><sort><creationdate>20170210</creationdate><title>Pan-retinal characterisation of Light Responses from Ganglion Cells in the Developing Mouse Retina</title><author>Hilgen, Gerrit ; 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Using a large-scale, high-density multielectrode array, we recorded from hundreds to thousands of RGCs simultaneously at pan-retinal level, including dorsal and ventral locations. Responses to different contrasts not only revealed a complex developmental profile for ON, OFF and ON-OFF responses, but also unveiled differences between dorsal and ventral RGC responses. At eye-opening, dorsal RGCs of all types were more responsive to light, perhaps indicating an environmental priority to nest viewing for pre-weaning pups. The developmental profile of ON and OFF responses exhibited antagonistic behaviour, with the strongest ON responses shortly after eye-opening, followed by an increase in the strength of OFF responses later on. Further, we found that with maturation receptive field (RF) center sizes decrease, spike-triggered averaged responses to white noise become stronger, and centers become more circular while maintaining differences between RGC types. We conclude that the maturation of retinal functionality is not spatially homogeneous, likely reflecting ecological requirements that favour earlier maturation of the dorsal retina.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>28186129</pmid><doi>10.1038/srep42330</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-4906-1368</orcidid><orcidid>https://orcid.org/0000-0003-1523-4187</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/378/2571/1696 631/378/3917 64/60 9/10 9/30 Action Potentials - radiation effects Aging - physiology Animals Electrodes Eye Humanities and Social Sciences Life Sciences Mice, Inbred C57BL multidisciplinary Neurons and Cognition Ontogeny Receptive field Retina Retinal ganglion cells Retinal Ganglion Cells - cytology Retinal Ganglion Cells - physiology Retinal Ganglion Cells - radiation effects Rodents Science Time Factors Weaning |
title | Pan-retinal characterisation of Light Responses from Ganglion Cells in the Developing Mouse Retina |
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