Cargando…

A Transient Translaminar GABAergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal Somatosensory Cortex

GABAergic activity is thought to influence developing neocortical sensory circuits. Yet the late postnatal maturation of local layer (L)4 circuits suggests alternate sources of GABAergic control in nascent thalamocortical networks. We show that a population of L5b, somatostatin (SST)-positive intern...

Descripción completa

Detalles Bibliográficos
Autores principales: Marques-Smith, Andre, Lyngholm, Daniel, Kaufmann, Anna-Kristin, Stacey, Jacqueline A., Hoerder-Suabedissen, Anna, Becker, Esther B.E., Wilson, Michael C., Molnár, Zoltán, Butt, Simon J.B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742537/
https://www.ncbi.nlm.nih.gov/pubmed/26844833
http://dx.doi.org/10.1016/j.neuron.2016.01.015
_version_ 1782414210830958592
author Marques-Smith, Andre
Lyngholm, Daniel
Kaufmann, Anna-Kristin
Stacey, Jacqueline A.
Hoerder-Suabedissen, Anna
Becker, Esther B.E.
Wilson, Michael C.
Molnár, Zoltán
Butt, Simon J.B.
author_facet Marques-Smith, Andre
Lyngholm, Daniel
Kaufmann, Anna-Kristin
Stacey, Jacqueline A.
Hoerder-Suabedissen, Anna
Becker, Esther B.E.
Wilson, Michael C.
Molnár, Zoltán
Butt, Simon J.B.
author_sort Marques-Smith, Andre
collection PubMed
description GABAergic activity is thought to influence developing neocortical sensory circuits. Yet the late postnatal maturation of local layer (L)4 circuits suggests alternate sources of GABAergic control in nascent thalamocortical networks. We show that a population of L5b, somatostatin (SST)-positive interneuron receives early thalamic synaptic input and, using laser-scanning photostimulation, identify an early transient circuit between these cells and L4 spiny stellates (SSNs) that disappears by the end of the L4 critical period. Sensory perturbation disrupts the transition to a local GABAergic circuit, suggesting a link between translaminar and local control of SSNs. Conditional silencing of SST+ interneurons or conversely biasing the circuit toward local inhibition by overexpression of neuregulin-1 type 1 results in an absence of early L5b GABAergic input in mutants and delayed thalamic innervation of SSNs. These data identify a role for L5b SST+ interneurons in the control of SSNs in the early postnatal neocortex.
format Online
Article
Text
id pubmed-4742537
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Cell Press
record_format MEDLINE/PubMed
spelling pubmed-47425372016-02-26 A Transient Translaminar GABAergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal Somatosensory Cortex Marques-Smith, Andre Lyngholm, Daniel Kaufmann, Anna-Kristin Stacey, Jacqueline A. Hoerder-Suabedissen, Anna Becker, Esther B.E. Wilson, Michael C. Molnár, Zoltán Butt, Simon J.B. Neuron Article GABAergic activity is thought to influence developing neocortical sensory circuits. Yet the late postnatal maturation of local layer (L)4 circuits suggests alternate sources of GABAergic control in nascent thalamocortical networks. We show that a population of L5b, somatostatin (SST)-positive interneuron receives early thalamic synaptic input and, using laser-scanning photostimulation, identify an early transient circuit between these cells and L4 spiny stellates (SSNs) that disappears by the end of the L4 critical period. Sensory perturbation disrupts the transition to a local GABAergic circuit, suggesting a link between translaminar and local control of SSNs. Conditional silencing of SST+ interneurons or conversely biasing the circuit toward local inhibition by overexpression of neuregulin-1 type 1 results in an absence of early L5b GABAergic input in mutants and delayed thalamic innervation of SSNs. These data identify a role for L5b SST+ interneurons in the control of SSNs in the early postnatal neocortex. Cell Press 2016-02-03 /pmc/articles/PMC4742537/ /pubmed/26844833 http://dx.doi.org/10.1016/j.neuron.2016.01.015 Text en © 2016 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
Marques-Smith, Andre
Lyngholm, Daniel
Kaufmann, Anna-Kristin
Stacey, Jacqueline A.
Hoerder-Suabedissen, Anna
Becker, Esther B.E.
Wilson, Michael C.
Molnár, Zoltán
Butt, Simon J.B.
A Transient Translaminar GABAergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal Somatosensory Cortex
title A Transient Translaminar GABAergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal Somatosensory Cortex
title_full A Transient Translaminar GABAergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal Somatosensory Cortex
title_fullStr A Transient Translaminar GABAergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal Somatosensory Cortex
title_full_unstemmed A Transient Translaminar GABAergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal Somatosensory Cortex
title_short A Transient Translaminar GABAergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal Somatosensory Cortex
title_sort transient translaminar gabaergic interneuron circuit connects thalamocortical recipient layers in neonatal somatosensory cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742537/
https://www.ncbi.nlm.nih.gov/pubmed/26844833
http://dx.doi.org/10.1016/j.neuron.2016.01.015
work_keys_str_mv AT marquessmithandre atransienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT lyngholmdaniel atransienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT kaufmannannakristin atransienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT staceyjacquelinea atransienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT hoerdersuabedissenanna atransienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT beckerestherbe atransienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT wilsonmichaelc atransienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT molnarzoltan atransienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT buttsimonjb atransienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT marquessmithandre transienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT lyngholmdaniel transienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT kaufmannannakristin transienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT staceyjacquelinea transienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT hoerdersuabedissenanna transienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT beckerestherbe transienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT wilsonmichaelc transienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT molnarzoltan transienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex
AT buttsimonjb transienttranslaminargabaergicinterneuroncircuitconnectsthalamocorticalrecipientlayersinneonatalsomatosensorycortex