Cargando…

A plasma membrane microdomain compartmentalizes ephrin-generated cAMP signals to prune developing retinal axon arbors

The development of neuronal circuits is controlled by guidance molecules that are hypothesized to interact with the cholesterol-enriched domains of the plasma membrane termed lipid rafts. Whether such domains enable local intracellular signalling at the submicrometre scale in developing neurons and...

Descripción completa

Detalles Bibliográficos
Autores principales: Averaimo, Stefania, Assali, Ahlem, Ros, Oriol, Couvet, Sandrine, Zagar, Yvrick, Genescu, Ioana, Rebsam, Alexandra, Nicol, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059439/
https://www.ncbi.nlm.nih.gov/pubmed/27694812
http://dx.doi.org/10.1038/ncomms12896
_version_ 1782459404463898624
author Averaimo, Stefania
Assali, Ahlem
Ros, Oriol
Couvet, Sandrine
Zagar, Yvrick
Genescu, Ioana
Rebsam, Alexandra
Nicol, Xavier
author_facet Averaimo, Stefania
Assali, Ahlem
Ros, Oriol
Couvet, Sandrine
Zagar, Yvrick
Genescu, Ioana
Rebsam, Alexandra
Nicol, Xavier
author_sort Averaimo, Stefania
collection PubMed
description The development of neuronal circuits is controlled by guidance molecules that are hypothesized to interact with the cholesterol-enriched domains of the plasma membrane termed lipid rafts. Whether such domains enable local intracellular signalling at the submicrometre scale in developing neurons and are required for shaping the nervous system connectivity in vivo remains controversial. Here, we report a role for lipid rafts in generating domains of local cAMP signalling in axonal growth cones downstream of ephrin-A repulsive guidance cues. Ephrin-A-dependent retraction of retinal ganglion cell axons involves cAMP signalling restricted to the vicinity of lipid rafts and is independent of cAMP modulation outside of this microdomain. cAMP modulation near lipid rafts controls the pruning of ectopic axonal branches of retinal ganglion cells in vivo, a process requiring intact ephrin-A signalling. Together, our findings indicate that lipid rafts structure the subcellular organization of intracellular cAMP signalling shaping axonal arbors during the nervous system development.
format Online
Article
Text
id pubmed-5059439
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-50594392016-10-26 A plasma membrane microdomain compartmentalizes ephrin-generated cAMP signals to prune developing retinal axon arbors Averaimo, Stefania Assali, Ahlem Ros, Oriol Couvet, Sandrine Zagar, Yvrick Genescu, Ioana Rebsam, Alexandra Nicol, Xavier Nat Commun Article The development of neuronal circuits is controlled by guidance molecules that are hypothesized to interact with the cholesterol-enriched domains of the plasma membrane termed lipid rafts. Whether such domains enable local intracellular signalling at the submicrometre scale in developing neurons and are required for shaping the nervous system connectivity in vivo remains controversial. Here, we report a role for lipid rafts in generating domains of local cAMP signalling in axonal growth cones downstream of ephrin-A repulsive guidance cues. Ephrin-A-dependent retraction of retinal ganglion cell axons involves cAMP signalling restricted to the vicinity of lipid rafts and is independent of cAMP modulation outside of this microdomain. cAMP modulation near lipid rafts controls the pruning of ectopic axonal branches of retinal ganglion cells in vivo, a process requiring intact ephrin-A signalling. Together, our findings indicate that lipid rafts structure the subcellular organization of intracellular cAMP signalling shaping axonal arbors during the nervous system development. Nature Publishing Group 2016-10-03 /pmc/articles/PMC5059439/ /pubmed/27694812 http://dx.doi.org/10.1038/ncomms12896 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Averaimo, Stefania
Assali, Ahlem
Ros, Oriol
Couvet, Sandrine
Zagar, Yvrick
Genescu, Ioana
Rebsam, Alexandra
Nicol, Xavier
A plasma membrane microdomain compartmentalizes ephrin-generated cAMP signals to prune developing retinal axon arbors
title A plasma membrane microdomain compartmentalizes ephrin-generated cAMP signals to prune developing retinal axon arbors
title_full A plasma membrane microdomain compartmentalizes ephrin-generated cAMP signals to prune developing retinal axon arbors
title_fullStr A plasma membrane microdomain compartmentalizes ephrin-generated cAMP signals to prune developing retinal axon arbors
title_full_unstemmed A plasma membrane microdomain compartmentalizes ephrin-generated cAMP signals to prune developing retinal axon arbors
title_short A plasma membrane microdomain compartmentalizes ephrin-generated cAMP signals to prune developing retinal axon arbors
title_sort plasma membrane microdomain compartmentalizes ephrin-generated camp signals to prune developing retinal axon arbors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059439/
https://www.ncbi.nlm.nih.gov/pubmed/27694812
http://dx.doi.org/10.1038/ncomms12896
work_keys_str_mv AT averaimostefania aplasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT assaliahlem aplasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT rosoriol aplasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT couvetsandrine aplasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT zagaryvrick aplasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT genescuioana aplasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT rebsamalexandra aplasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT nicolxavier aplasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT averaimostefania plasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT assaliahlem plasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT rosoriol plasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT couvetsandrine plasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT zagaryvrick plasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT genescuioana plasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT rebsamalexandra plasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors
AT nicolxavier plasmamembranemicrodomaincompartmentalizesephringeneratedcampsignalstoprunedevelopingretinalaxonarbors