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Learning-Related Plasticity in Dendrite-Targeting Layer 1 Interneurons
A wealth of data has elucidated the mechanisms by which sensory inputs are encoded in the neocortex, but how these processes are regulated by the behavioral relevance of sensory information is less understood. Here, we focus on neocortical layer 1 (L1), a key location for processing of such top-down...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226614/ https://www.ncbi.nlm.nih.gov/pubmed/30269988 http://dx.doi.org/10.1016/j.neuron.2018.09.001 |
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author | Abs, Elisabeth Poorthuis, Rogier B. Apelblat, Daniella Muhammad, Karzan Pardi, M. Belen Enke, Leona Kushinsky, Dahlia Pu, De-Lin Eizinger, Max Ferdinand Conzelmann, Karl-Klaus Spiegel, Ivo Letzkus, Johannes J. |
author_facet | Abs, Elisabeth Poorthuis, Rogier B. Apelblat, Daniella Muhammad, Karzan Pardi, M. Belen Enke, Leona Kushinsky, Dahlia Pu, De-Lin Eizinger, Max Ferdinand Conzelmann, Karl-Klaus Spiegel, Ivo Letzkus, Johannes J. |
author_sort | Abs, Elisabeth |
collection | PubMed |
description | A wealth of data has elucidated the mechanisms by which sensory inputs are encoded in the neocortex, but how these processes are regulated by the behavioral relevance of sensory information is less understood. Here, we focus on neocortical layer 1 (L1), a key location for processing of such top-down information. Using Neuron-Derived Neurotrophic Factor (NDNF) as a selective marker of L1 interneurons (INs) and in vivo 2-photon calcium imaging, electrophysiology, viral tracing, optogenetics, and associative memory, we find that L1 NDNF-INs mediate a prolonged form of inhibition in distal pyramidal neuron dendrites that correlates with the strength of the memory trace. Conversely, inhibition from Martinotti cells remains unchanged after conditioning but in turn tightly controls sensory responses in NDNF-INs. These results define a genetically addressable form of dendritic inhibition that is highly experience dependent and indicate that in addition to disinhibition, salient stimuli are encoded at elevated levels of distal dendritic inhibition. VIDEO ABSTRACT: |
format | Online Article Text |
id | pubmed-6226614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62266142018-11-16 Learning-Related Plasticity in Dendrite-Targeting Layer 1 Interneurons Abs, Elisabeth Poorthuis, Rogier B. Apelblat, Daniella Muhammad, Karzan Pardi, M. Belen Enke, Leona Kushinsky, Dahlia Pu, De-Lin Eizinger, Max Ferdinand Conzelmann, Karl-Klaus Spiegel, Ivo Letzkus, Johannes J. Neuron Article A wealth of data has elucidated the mechanisms by which sensory inputs are encoded in the neocortex, but how these processes are regulated by the behavioral relevance of sensory information is less understood. Here, we focus on neocortical layer 1 (L1), a key location for processing of such top-down information. Using Neuron-Derived Neurotrophic Factor (NDNF) as a selective marker of L1 interneurons (INs) and in vivo 2-photon calcium imaging, electrophysiology, viral tracing, optogenetics, and associative memory, we find that L1 NDNF-INs mediate a prolonged form of inhibition in distal pyramidal neuron dendrites that correlates with the strength of the memory trace. Conversely, inhibition from Martinotti cells remains unchanged after conditioning but in turn tightly controls sensory responses in NDNF-INs. These results define a genetically addressable form of dendritic inhibition that is highly experience dependent and indicate that in addition to disinhibition, salient stimuli are encoded at elevated levels of distal dendritic inhibition. VIDEO ABSTRACT: Cell Press 2018-11-07 /pmc/articles/PMC6226614/ /pubmed/30269988 http://dx.doi.org/10.1016/j.neuron.2018.09.001 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Abs, Elisabeth Poorthuis, Rogier B. Apelblat, Daniella Muhammad, Karzan Pardi, M. Belen Enke, Leona Kushinsky, Dahlia Pu, De-Lin Eizinger, Max Ferdinand Conzelmann, Karl-Klaus Spiegel, Ivo Letzkus, Johannes J. Learning-Related Plasticity in Dendrite-Targeting Layer 1 Interneurons |
title | Learning-Related Plasticity in Dendrite-Targeting Layer 1 Interneurons |
title_full | Learning-Related Plasticity in Dendrite-Targeting Layer 1 Interneurons |
title_fullStr | Learning-Related Plasticity in Dendrite-Targeting Layer 1 Interneurons |
title_full_unstemmed | Learning-Related Plasticity in Dendrite-Targeting Layer 1 Interneurons |
title_short | Learning-Related Plasticity in Dendrite-Targeting Layer 1 Interneurons |
title_sort | learning-related plasticity in dendrite-targeting layer 1 interneurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226614/ https://www.ncbi.nlm.nih.gov/pubmed/30269988 http://dx.doi.org/10.1016/j.neuron.2018.09.001 |
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