Summary: Researchers report cells can pack and releases active ephrins and Eph receptors through extracellular vesicles.
Source: Max Planck Institute.
Signaling molecules can make neuronal extensions retract at a distance.
Eph receptors and their partner proteins, the ephrins, are vital for intercellular communication. In the developing brain, they guide young neurons to the right partner cells by repulsion. They also play important roles in cell migration, regeneration, neurodegenerative diseases and the development of cancer. Until recently, scientists assumed that ephrin/Eph signal transmission could only occur through direct cell-cell contact. However, Rüdiger Klein and his team at the Max Planck Institute of Neurobiology have now shown that cells can also pack and release active ephrins and Eph receptors through extracellular vesicles. Not only does this discovery improve our understanding of this communication system, it may also pave the way for new therapeutic strategies.
The human body contains up to 100 billion cells. As they grow, migrate, replicate and move, these cells come into contact with countless other cells and exchange information with them. One way this communication happens is through the ephrin/Eph-receptor system, which is able to guide cell migration and the growth of neuronal extensions. In addition, the ephrin-Eph system also plays a role in plastic processes, such as learning and regeneration, as well as in tumour growth and neurodegenerative diseases.
Eph receptors and their binding partners, the ephrins, are found on the surface of almost all cell types. When an ephrin meets the Eph receptor of another cell, they join to form an ephrin-Eph complex. This triggers processes in one or both cells that generally lead to internalization of the complex and repulsion of one cell away from the other. The repelled cell then moves or grows in another direction. In the nervous system, many such interactions guide the extensions of young neurons to their right destinations.
“This is why it’s so fundamentally important to understand how cells use this system to communicate”, says Rüdiger Klein, whose Department at the Max Planck Institute of Neurobiology is studying ephrins and Eph receptors. It had always seemed clear that ephrins and Ephs could only trigger a signaling process by direct contact between two cells. Recently, however, ephrins and Eph receptors have also been found in extracellular vesicles/exosomes – small droplets of fat released by cells, used as transport vehicles, signal transmitters or for eliminating cell components. “This has thrown up the interesting question of what business Ephs and ephrins have in exosomes”, says Klein.
Intrigued, the Martinsried-based team set up an elaborate experimental study to purify the exosomes from different cell types, including neurons, and analyse their contents. They revealed that many of these exosomes contained ephrins and Ephs, and decoded the cellular mechanism by which they were packed into the exosomes. Interestingly, further analysis showed that the Eph receptors had not been dumped as waste products, but remained active on the exosomes. Eph receptors on the exosomes were able to bind to ephrin molecules on the surface of growing neurons and repel the neuronal extensions. This proves, for the first time, that cells can send ephrins and Ephs out to transmit signals over a distance. “It opens up a whole range of new possibilities”, says Rüdiger Klein. Ephrins and Eph receptors have also been found in the exosomes of cancer cells. “This might mean that strategies to control exosome release could be used to interrupt the ephrin-Eph signaling pathway and thereby disrupt tumour growth”, he surmises.
About this neuroscience research article
Source: Stefanie Merker – Max Planck Institute Image Source: This NeuroscienceNews.com image is credited to MPI of Neurobiology / Gong. Original Research:Abstract for “Exosomes mediate cell contact-independent ephrin-Eph signaling during axon guidance” by Jingyi Gong, Roman Körner, Louise Gaitanos, and Rüdiger Klein in Journal of Cell Biology. Published online June 27 2016 doi:1083/jcb.201601085
Cite This NeuroscienceNews.com Article
[cbtabs][cbtab title=”MLA”]Max Planck Institute. “Cells Send Out Stop Signals.” NeuroscienceNews. NeuroscienceNews, 5 July 2016. <https://neurosciencenews.com/distance-neuronal-extensions-4617/>.[/cbtab][cbtab title=”APA”]Max Planck Institute. (2016, July 5). Cells Send Out Stop Signals. NeuroscienceNews. Retrieved July 5, 2016 from https://neurosciencenews.com/distance-neuronal-extensions-4617/[/cbtab][cbtab title=”Chicago”]Max Planck Institute. “Cells Send Out Stop Signals.” https://neurosciencenews.com/distance-neuronal-extensions-4617/ (accessed July 5, 2016).[/cbtab][/cbtabs]
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 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.
“Exosomes mediate cell contact-independent ephrin-Eph signaling during axon guidance” by Jingyi Gong, Roman Körner, Louise Gaitanos, and Rüdiger Klein in Journal of Cell Biology. Published online June 27 2016 doi:1083/jcb.201601085