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IgSF11 homophilic adhesion proteins promote layer-specific synaptic assembly of the cortical interneuron subtype

The most prominent structural hallmark of the mammalian neocortical circuitry is the layer-based organization of specific cell types and synaptic inputs. Accordingly, cortical inhibitory interneurons (INs), which shape local network activity, exhibit subtype-specific laminar specificity of synaptic...

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Autores principales: Hayano, Yasufumi, Ishino, Yugo, Hyun, Jung Ho, Orozco, Carlos G., Steinecke, André, Potts, Elizabeth, Oisi, Yasuhiro, Thomas, Connon I., Guerrero-Given, Debbie, Kim, Eunjoon, Kwon, Hyung-Bae, Kamasawa, Naomi, Taniguchi, Hiroki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8279514/
https://www.ncbi.nlm.nih.gov/pubmed/34261648
http://dx.doi.org/10.1126/sciadv.abf1600
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author Hayano, Yasufumi
Ishino, Yugo
Hyun, Jung Ho
Orozco, Carlos G.
Steinecke, André
Potts, Elizabeth
Oisi, Yasuhiro
Thomas, Connon I.
Guerrero-Given, Debbie
Kim, Eunjoon
Kwon, Hyung-Bae
Kamasawa, Naomi
Taniguchi, Hiroki
author_facet Hayano, Yasufumi
Ishino, Yugo
Hyun, Jung Ho
Orozco, Carlos G.
Steinecke, André
Potts, Elizabeth
Oisi, Yasuhiro
Thomas, Connon I.
Guerrero-Given, Debbie
Kim, Eunjoon
Kwon, Hyung-Bae
Kamasawa, Naomi
Taniguchi, Hiroki
author_sort Hayano, Yasufumi
collection PubMed
description The most prominent structural hallmark of the mammalian neocortical circuitry is the layer-based organization of specific cell types and synaptic inputs. Accordingly, cortical inhibitory interneurons (INs), which shape local network activity, exhibit subtype-specific laminar specificity of synaptic outputs. However, the underlying molecular mechanisms remain unknown. Here, we demonstrate that Immunoglobulin Superfamily member 11 (IgSF11) homophilic adhesion proteins are preferentially expressed in one of the most distinctive IN subtypes, namely, chandelier cells (ChCs) that specifically innervate axon initial segments of pyramidal neurons (PNs), and their synaptic laminar target. Loss-of-function experiments in either ChCs or postsynaptic cells revealed that IgSF11 is required for ChC synaptic development in the target layer. While overexpression of IgSF11 in ChCs enlarges ChC presynaptic boutons, expressing IgSF11 in nontarget layers induces ectopic ChC synapses. These findings provide evidence that synapse-promoting adhesion proteins, highly localized to synaptic partners, determine the layer-specific synaptic connectivity of the cortical IN subtype.
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spelling pubmed-82795142021-07-16 IgSF11 homophilic adhesion proteins promote layer-specific synaptic assembly of the cortical interneuron subtype Hayano, Yasufumi Ishino, Yugo Hyun, Jung Ho Orozco, Carlos G. Steinecke, André Potts, Elizabeth Oisi, Yasuhiro Thomas, Connon I. Guerrero-Given, Debbie Kim, Eunjoon Kwon, Hyung-Bae Kamasawa, Naomi Taniguchi, Hiroki Sci Adv Research Articles The most prominent structural hallmark of the mammalian neocortical circuitry is the layer-based organization of specific cell types and synaptic inputs. Accordingly, cortical inhibitory interneurons (INs), which shape local network activity, exhibit subtype-specific laminar specificity of synaptic outputs. However, the underlying molecular mechanisms remain unknown. Here, we demonstrate that Immunoglobulin Superfamily member 11 (IgSF11) homophilic adhesion proteins are preferentially expressed in one of the most distinctive IN subtypes, namely, chandelier cells (ChCs) that specifically innervate axon initial segments of pyramidal neurons (PNs), and their synaptic laminar target. Loss-of-function experiments in either ChCs or postsynaptic cells revealed that IgSF11 is required for ChC synaptic development in the target layer. While overexpression of IgSF11 in ChCs enlarges ChC presynaptic boutons, expressing IgSF11 in nontarget layers induces ectopic ChC synapses. These findings provide evidence that synapse-promoting adhesion proteins, highly localized to synaptic partners, determine the layer-specific synaptic connectivity of the cortical IN subtype. American Association for the Advancement of Science 2021-07-14 /pmc/articles/PMC8279514/ /pubmed/34261648 http://dx.doi.org/10.1126/sciadv.abf1600 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Hayano, Yasufumi
Ishino, Yugo
Hyun, Jung Ho
Orozco, Carlos G.
Steinecke, André
Potts, Elizabeth
Oisi, Yasuhiro
Thomas, Connon I.
Guerrero-Given, Debbie
Kim, Eunjoon
Kwon, Hyung-Bae
Kamasawa, Naomi
Taniguchi, Hiroki
IgSF11 homophilic adhesion proteins promote layer-specific synaptic assembly of the cortical interneuron subtype
title IgSF11 homophilic adhesion proteins promote layer-specific synaptic assembly of the cortical interneuron subtype
title_full IgSF11 homophilic adhesion proteins promote layer-specific synaptic assembly of the cortical interneuron subtype
title_fullStr IgSF11 homophilic adhesion proteins promote layer-specific synaptic assembly of the cortical interneuron subtype
title_full_unstemmed IgSF11 homophilic adhesion proteins promote layer-specific synaptic assembly of the cortical interneuron subtype
title_short IgSF11 homophilic adhesion proteins promote layer-specific synaptic assembly of the cortical interneuron subtype
title_sort igsf11 homophilic adhesion proteins promote layer-specific synaptic assembly of the cortical interneuron subtype
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8279514/
https://www.ncbi.nlm.nih.gov/pubmed/34261648
http://dx.doi.org/10.1126/sciadv.abf1600
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