Cargando…

Distinct mechanisms of spike timing‐dependent LTD at vertical and horizontal inputs onto L2/3 pyramidal neurons in mouse barrel cortex

Spike timing‐dependent plasticity (STDP) is an attractive candidate to mediate the synaptic changes that support circuit plasticity in sensory cortices during development. STDP is prevalent at excitatory synapses, but it is not known whether the underlying mechanisms are universal, or whether distin...

Descripción completa

Detalles Bibliográficos
Autores principales: Banerjee, Abhishek, González‐Rueda, Ana, Sampaio‐Baptista, Cassandra, Paulsen, Ole, Rodríguez‐Moreno, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4002250/
https://www.ncbi.nlm.nih.gov/pubmed/24760524
http://dx.doi.org/10.1002/phy2.271
_version_ 1782313793038057472
author Banerjee, Abhishek
González‐Rueda, Ana
Sampaio‐Baptista, Cassandra
Paulsen, Ole
Rodríguez‐Moreno, Antonio
author_facet Banerjee, Abhishek
González‐Rueda, Ana
Sampaio‐Baptista, Cassandra
Paulsen, Ole
Rodríguez‐Moreno, Antonio
author_sort Banerjee, Abhishek
collection PubMed
description Spike timing‐dependent plasticity (STDP) is an attractive candidate to mediate the synaptic changes that support circuit plasticity in sensory cortices during development. STDP is prevalent at excitatory synapses, but it is not known whether the underlying mechanisms are universal, or whether distinct mechanisms underpin STDP at different synapses. Here, we set out to compare and contrast STDP at vertical layer 4 and horizontal layer 2/3 inputs onto postsynaptic layer 2/3 neurons in the mouse barrel cortex. We find that both vertical and horizontal inputs show STDP, but that they display different time windows for induction of timing‐dependent long‐term depression (t‐LTD). Moreover, whereas t‐LTD at vertical inputs requires presynaptic NMDA receptors and is expressed presynaptically, using paired recordings we find that t‐LTD at horizontal inputs requires postsynaptic NMDA receptors and is expressed postsynaptically. These results demonstrate that similar forms of plasticity on the same postsynaptic neuron can be mediated by distinct mechanisms, and suggest that these forms of plasticity may enable these two types of cortical synapses to support different functions.
format Online
Article
Text
id pubmed-4002250
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Wiley Periodicals, Inc.
record_format MEDLINE/PubMed
spelling pubmed-40022502014-05-13 Distinct mechanisms of spike timing‐dependent LTD at vertical and horizontal inputs onto L2/3 pyramidal neurons in mouse barrel cortex Banerjee, Abhishek González‐Rueda, Ana Sampaio‐Baptista, Cassandra Paulsen, Ole Rodríguez‐Moreno, Antonio Physiol Rep Original Research Spike timing‐dependent plasticity (STDP) is an attractive candidate to mediate the synaptic changes that support circuit plasticity in sensory cortices during development. STDP is prevalent at excitatory synapses, but it is not known whether the underlying mechanisms are universal, or whether distinct mechanisms underpin STDP at different synapses. Here, we set out to compare and contrast STDP at vertical layer 4 and horizontal layer 2/3 inputs onto postsynaptic layer 2/3 neurons in the mouse barrel cortex. We find that both vertical and horizontal inputs show STDP, but that they display different time windows for induction of timing‐dependent long‐term depression (t‐LTD). Moreover, whereas t‐LTD at vertical inputs requires presynaptic NMDA receptors and is expressed presynaptically, using paired recordings we find that t‐LTD at horizontal inputs requires postsynaptic NMDA receptors and is expressed postsynaptically. These results demonstrate that similar forms of plasticity on the same postsynaptic neuron can be mediated by distinct mechanisms, and suggest that these forms of plasticity may enable these two types of cortical synapses to support different functions. Wiley Periodicals, Inc. 2014-03-26 /pmc/articles/PMC4002250/ /pubmed/24760524 http://dx.doi.org/10.1002/phy2.271 Text en © 2014 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Banerjee, Abhishek
González‐Rueda, Ana
Sampaio‐Baptista, Cassandra
Paulsen, Ole
Rodríguez‐Moreno, Antonio
Distinct mechanisms of spike timing‐dependent LTD at vertical and horizontal inputs onto L2/3 pyramidal neurons in mouse barrel cortex
title Distinct mechanisms of spike timing‐dependent LTD at vertical and horizontal inputs onto L2/3 pyramidal neurons in mouse barrel cortex
title_full Distinct mechanisms of spike timing‐dependent LTD at vertical and horizontal inputs onto L2/3 pyramidal neurons in mouse barrel cortex
title_fullStr Distinct mechanisms of spike timing‐dependent LTD at vertical and horizontal inputs onto L2/3 pyramidal neurons in mouse barrel cortex
title_full_unstemmed Distinct mechanisms of spike timing‐dependent LTD at vertical and horizontal inputs onto L2/3 pyramidal neurons in mouse barrel cortex
title_short Distinct mechanisms of spike timing‐dependent LTD at vertical and horizontal inputs onto L2/3 pyramidal neurons in mouse barrel cortex
title_sort distinct mechanisms of spike timing‐dependent ltd at vertical and horizontal inputs onto l2/3 pyramidal neurons in mouse barrel cortex
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4002250/
https://www.ncbi.nlm.nih.gov/pubmed/24760524
http://dx.doi.org/10.1002/phy2.271
work_keys_str_mv AT banerjeeabhishek distinctmechanismsofspiketimingdependentltdatverticalandhorizontalinputsontol23pyramidalneuronsinmousebarrelcortex
AT gonzalezruedaana distinctmechanismsofspiketimingdependentltdatverticalandhorizontalinputsontol23pyramidalneuronsinmousebarrelcortex
AT sampaiobaptistacassandra distinctmechanismsofspiketimingdependentltdatverticalandhorizontalinputsontol23pyramidalneuronsinmousebarrelcortex
AT paulsenole distinctmechanismsofspiketimingdependentltdatverticalandhorizontalinputsontol23pyramidalneuronsinmousebarrelcortex
AT rodriguezmorenoantonio distinctmechanismsofspiketimingdependentltdatverticalandhorizontalinputsontol23pyramidalneuronsinmousebarrelcortex