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TSPAN5 Enriched Microdomains Provide a Platform for Dendritic Spine Maturation through Neuroligin-1 Clustering

Tetraspanins are a class of evolutionarily conserved transmembrane proteins with 33 members identified in mammals that have the ability to organize specific membrane domains, named tetraspanin-enriched microdomains (TEMs). Despite the relative abundance of different tetraspanins in the CNS, few stud...

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Autores principales: Moretto, Edoardo, Longatti, Anna, Murru, Luca, Chamma, Ingrid, Sessa, Alessandro, Zapata, Jonathan, Hosy, Eric, Sainlos, Matthieu, Saint-Pol, Julien, Rubinstein, Eric, Choquet, Daniel, Broccoli, Vania, Schiavo, Giampietro, Thoumine, Olivier, Passafaro, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899445/
https://www.ncbi.nlm.nih.gov/pubmed/31665629
http://dx.doi.org/10.1016/j.celrep.2019.09.051
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author Moretto, Edoardo
Longatti, Anna
Murru, Luca
Chamma, Ingrid
Sessa, Alessandro
Zapata, Jonathan
Hosy, Eric
Sainlos, Matthieu
Saint-Pol, Julien
Rubinstein, Eric
Choquet, Daniel
Broccoli, Vania
Schiavo, Giampietro
Thoumine, Olivier
Passafaro, Maria
author_facet Moretto, Edoardo
Longatti, Anna
Murru, Luca
Chamma, Ingrid
Sessa, Alessandro
Zapata, Jonathan
Hosy, Eric
Sainlos, Matthieu
Saint-Pol, Julien
Rubinstein, Eric
Choquet, Daniel
Broccoli, Vania
Schiavo, Giampietro
Thoumine, Olivier
Passafaro, Maria
author_sort Moretto, Edoardo
collection PubMed
description Tetraspanins are a class of evolutionarily conserved transmembrane proteins with 33 members identified in mammals that have the ability to organize specific membrane domains, named tetraspanin-enriched microdomains (TEMs). Despite the relative abundance of different tetraspanins in the CNS, few studies have explored their role at synapses. Here, we investigate the function of TSPAN5, a member of the tetraspanin superfamily for which mRNA transcripts are found at high levels in the mouse brain. We demonstrate that TSPAN5 is localized in dendritic spines of pyramidal excitatory neurons and that TSPAN5 knockdown induces a dramatic decrease in spine number because of defects in the spine maturation process. Moreover, we show that TSPAN5 interacts with the postsynaptic adhesion molecule neuroligin-1, promoting its correct surface clustering. We propose that membrane compartmentalization by tetraspanins represents an additional mechanism for regulating excitatory synapses.
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spelling pubmed-68994452020-01-21 TSPAN5 Enriched Microdomains Provide a Platform for Dendritic Spine Maturation through Neuroligin-1 Clustering Moretto, Edoardo Longatti, Anna Murru, Luca Chamma, Ingrid Sessa, Alessandro Zapata, Jonathan Hosy, Eric Sainlos, Matthieu Saint-Pol, Julien Rubinstein, Eric Choquet, Daniel Broccoli, Vania Schiavo, Giampietro Thoumine, Olivier Passafaro, Maria Cell Rep Article Tetraspanins are a class of evolutionarily conserved transmembrane proteins with 33 members identified in mammals that have the ability to organize specific membrane domains, named tetraspanin-enriched microdomains (TEMs). Despite the relative abundance of different tetraspanins in the CNS, few studies have explored their role at synapses. Here, we investigate the function of TSPAN5, a member of the tetraspanin superfamily for which mRNA transcripts are found at high levels in the mouse brain. We demonstrate that TSPAN5 is localized in dendritic spines of pyramidal excitatory neurons and that TSPAN5 knockdown induces a dramatic decrease in spine number because of defects in the spine maturation process. Moreover, we show that TSPAN5 interacts with the postsynaptic adhesion molecule neuroligin-1, promoting its correct surface clustering. We propose that membrane compartmentalization by tetraspanins represents an additional mechanism for regulating excitatory synapses. Cell Press 2019-10-30 /pmc/articles/PMC6899445/ /pubmed/31665629 http://dx.doi.org/10.1016/j.celrep.2019.09.051 Text en © 2019 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
Moretto, Edoardo
Longatti, Anna
Murru, Luca
Chamma, Ingrid
Sessa, Alessandro
Zapata, Jonathan
Hosy, Eric
Sainlos, Matthieu
Saint-Pol, Julien
Rubinstein, Eric
Choquet, Daniel
Broccoli, Vania
Schiavo, Giampietro
Thoumine, Olivier
Passafaro, Maria
TSPAN5 Enriched Microdomains Provide a Platform for Dendritic Spine Maturation through Neuroligin-1 Clustering
title TSPAN5 Enriched Microdomains Provide a Platform for Dendritic Spine Maturation through Neuroligin-1 Clustering
title_full TSPAN5 Enriched Microdomains Provide a Platform for Dendritic Spine Maturation through Neuroligin-1 Clustering
title_fullStr TSPAN5 Enriched Microdomains Provide a Platform for Dendritic Spine Maturation through Neuroligin-1 Clustering
title_full_unstemmed TSPAN5 Enriched Microdomains Provide a Platform for Dendritic Spine Maturation through Neuroligin-1 Clustering
title_short TSPAN5 Enriched Microdomains Provide a Platform for Dendritic Spine Maturation through Neuroligin-1 Clustering
title_sort tspan5 enriched microdomains provide a platform for dendritic spine maturation through neuroligin-1 clustering
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899445/
https://www.ncbi.nlm.nih.gov/pubmed/31665629
http://dx.doi.org/10.1016/j.celrep.2019.09.051
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