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

Gong, J., Körner, R., Gaitanos, L., & Klein, R. (2016). Exosomes mediate cell contact-independent ephrin-Eph signaling during axon guidance. The Journal of Cell Biology, 214(1), 35-44. doi:10.1083/jcb.201601085.

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 Urheber:
Gong, Jingyi1, Autor           
Körner, Roman2, Autor           
Gaitanos, Louise1, Autor           
Klein, Rüdiger1, Autor           
Affiliations:
1Department: Molecules-Signaling-Development / Klein, MPI of Neurobiology, Max Planck Society, ou_1113546              
2Hartl, Franz-Ulrich / Cellular Biochemistry, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565152              

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Schlagwörter: EXTRACELLULAR VESICLES; NERVOUS-SYSTEM; REPULSION; ENDOCYTOSIS; RECEPTORS; SECRETION; POPULATIONS; BIOGENESIS; PROTEOMICS; PROTEINSCell Biology;
 Zusammenfassung: 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.

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Sprache(n): eng - English
 Datum: 2016-01-252016-06-072016-06-272016
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: ISI: 000379283500007
DOI: 10.1083/jcb.201601085
 Art des Abschluß: -

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Projektname : This study was funded by the Max Planck Society and the Deutsche Forschungsgemeinschaft (SyNergy).
Grant ID : -
Förderprogramm : -
Förderorganisation : -

Quelle 1

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Titel: The Journal of Cell Biology
  Andere : JBC
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: New York, NY : Rockefeller Institute Press
Seiten: - Band / Heft: 214 (1) Artikelnummer: - Start- / Endseite: 35 - 44 Identifikator: ISSN: 0021-9525
CoNE: https://pure.mpg.de/cone/journals/resource/991042742946024_2