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

被引:109
作者
Gong, Jingyi [1 ,3 ]
Koerner, Roman [2 ,3 ]
Gaitanos, Louise [1 ]
Klein, Ruediger [1 ,3 ]
机构
[1] Max Planck Inst Neurobiol, D-82152 Martinsried, Germany
[2] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[3] Munich Cluster Syst Neurol SyNergy, D-80336 Munich, Germany
关键词
EXTRACELLULAR VESICLES; ENDOCYTOSIS; RECEPTORS; POPULATIONS; BIOGENESIS; REPULSION; SECRETION; PROTEINS; CLEAVAGE; ADHESION;
D O I
10.1083/jcb.201601085
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:35 / 44
页数:10
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