Cargando…

Exosomes mediate cell contact–independent ephrin-Eph signaling during axon guidance

The cellular release of membranous vesicles known as extracellular vesicles (EVs) or exosomes represents a novel mode of intercellular communication. Eph receptor tyrosine kinases and their membrane-tethered ephrin ligands have very important roles in such biologically diverse processes as neuronal...

Descripción completa

Detalles Bibliográficos
Autores principales: Gong, Jingyi, Körner, Roman, Gaitanos, Louise, Klein, Rüdiger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932373/
https://www.ncbi.nlm.nih.gov/pubmed/27354374
http://dx.doi.org/10.1083/jcb.201601085
_version_ 1782441052144140288
author Gong, Jingyi
Körner, Roman
Gaitanos, Louise
Klein, Rüdiger
author_facet Gong, Jingyi
Körner, Roman
Gaitanos, Louise
Klein, Rüdiger
author_sort Gong, Jingyi
collection PubMed
description The cellular release of membranous vesicles known as extracellular vesicles (EVs) or exosomes represents a novel mode of intercellular communication. Eph receptor tyrosine kinases and their membrane-tethered ephrin ligands have very important roles in such biologically diverse processes as neuronal development, plasticity, and pathological diseases. Until now, it was thought that ephrin-Eph signaling requires direct cell contact. Although the biological functions of ephrin-Eph signaling are well understood, our mechanistic understanding remains modest. Here we report the release of EVs containing Ephs and ephrins by different cell types, a process requiring endosomal sorting complex required for transport (ESCRT) activity and regulated by neuronal activity. Treatment of cells with purified EphB2(+) EVs induces ephrinB1 reverse signaling and causes neuronal axon repulsion. These results indicate a novel mechanism of ephrin-Eph signaling independent of direct cell contact and proteolytic cleavage and suggest the participation of EphB2(+) EVs in neural development and synapse physiology.
format Online
Article
Text
id pubmed-4932373
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-49323732017-01-04 Exosomes mediate cell contact–independent ephrin-Eph signaling during axon guidance Gong, Jingyi Körner, Roman Gaitanos, Louise Klein, Rüdiger J Cell Biol Research Articles The cellular release of membranous vesicles known as extracellular vesicles (EVs) or exosomes represents a novel mode of intercellular communication. Eph receptor tyrosine kinases and their membrane-tethered ephrin ligands have very important roles in such biologically diverse processes as neuronal development, plasticity, and pathological diseases. Until now, it was thought that ephrin-Eph signaling requires direct cell contact. Although the biological functions of ephrin-Eph signaling are well understood, our mechanistic understanding remains modest. Here we report the release of EVs containing Ephs and ephrins by different cell types, a process requiring endosomal sorting complex required for transport (ESCRT) activity and regulated by neuronal activity. Treatment of cells with purified EphB2(+) EVs induces ephrinB1 reverse signaling and causes neuronal axon repulsion. These results indicate a novel mechanism of ephrin-Eph signaling independent of direct cell contact and proteolytic cleavage and suggest the participation of EphB2(+) EVs in neural development and synapse physiology. The Rockefeller University Press 2016-07-04 /pmc/articles/PMC4932373/ /pubmed/27354374 http://dx.doi.org/10.1083/jcb.201601085 Text en © 2016 Gong et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Gong, Jingyi
Körner, Roman
Gaitanos, Louise
Klein, Rüdiger
Exosomes mediate cell contact–independent ephrin-Eph signaling during axon guidance
title Exosomes mediate cell contact–independent ephrin-Eph signaling during axon guidance
title_full Exosomes mediate cell contact–independent ephrin-Eph signaling during axon guidance
title_fullStr Exosomes mediate cell contact–independent ephrin-Eph signaling during axon guidance
title_full_unstemmed Exosomes mediate cell contact–independent ephrin-Eph signaling during axon guidance
title_short Exosomes mediate cell contact–independent ephrin-Eph signaling during axon guidance
title_sort exosomes mediate cell contact–independent ephrin-eph signaling during axon guidance
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932373/
https://www.ncbi.nlm.nih.gov/pubmed/27354374
http://dx.doi.org/10.1083/jcb.201601085
work_keys_str_mv AT gongjingyi exosomesmediatecellcontactindependentephrinephsignalingduringaxonguidance
AT kornerroman exosomesmediatecellcontactindependentephrinephsignalingduringaxonguidance
AT gaitanoslouise exosomesmediatecellcontactindependentephrinephsignalingduringaxonguidance
AT kleinrudiger exosomesmediatecellcontactindependentephrinephsignalingduringaxonguidance