Exosomes are small extracellular vesicles which stem from endosomes fusing with the plasma membrane; they contain lipids, proteins and RNAs that are able to modify receiving cells. Functioning of the brain relies on synapses, and certain patterns of synaptic activity can change the strength of responses at sparse groups of synapses, to modulate circuits underlying associations and memory. These local changes of the synaptic physiology in one neuron driven by another have, so far, been explained by classical signal transduction modulating transcription, translation and post-translational modifications. We have accumulated in vitro evidence that exosomes released by neurons in a way depending on synaptic activity can be recaptured by other neurons. Some lipids, proteins and RNAs contained in exosomes secreted by emitting neurons could directly modify signal transduction and protein expression in receiving cells. Exosomes may be an ideal mechanism for anterograde and retrograde information transfer across synapses underlying local changes in synaptic plasticity. Exosomes might also participate in the spreading across the nervous system of pathological proteins such as PrPSc (abnormal disease-specific conformation of prion protein), APP (amyloid precursor protein) fragments, phosphorylated tau or α-synuclein.
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February 2013
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Conference Article|
January 29 2013
Exosomes as a novel way of interneuronal communication
Mathilde Chivet;
Mathilde Chivet
*Inserm, U836, Equipe 2, Neurodégénérescence et Plasticité, Grenoble, France
†Université Joseph Fourier, Grenoble Institute of Neuroscience, Grenoble, France
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Charlotte Javalet;
Charlotte Javalet
*Inserm, U836, Equipe 2, Neurodégénérescence et Plasticité, Grenoble, France
†Université Joseph Fourier, Grenoble Institute of Neuroscience, Grenoble, France
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Fiona Hemming;
Fiona Hemming
*Inserm, U836, Equipe 2, Neurodégénérescence et Plasticité, Grenoble, France
†Université Joseph Fourier, Grenoble Institute of Neuroscience, Grenoble, France
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Karin Pernet-Gallay;
Karin Pernet-Gallay
†Université Joseph Fourier, Grenoble Institute of Neuroscience, Grenoble, France
‡Inserm, U836, Plateforme de microscopie, Grenoble, France
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Karine Laulagnier;
Karine Laulagnier
*Inserm, U836, Equipe 2, Neurodégénérescence et Plasticité, Grenoble, France
†Université Joseph Fourier, Grenoble Institute of Neuroscience, Grenoble, France
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Sandrine Fraboulet;
Sandrine Fraboulet
*Inserm, U836, Equipe 2, Neurodégénérescence et Plasticité, Grenoble, France
†Université Joseph Fourier, Grenoble Institute of Neuroscience, Grenoble, France
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Rémy Sadoul
Rémy Sadoul
1
*Inserm, U836, Equipe 2, Neurodégénérescence et Plasticité, Grenoble, France
†Université Joseph Fourier, Grenoble Institute of Neuroscience, Grenoble, France
1To whom correspondence should be addressed (emailremy.sadoul@ujf-grenoble.fr).
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Biochem Soc Trans (2013) 41 (1): 241–244.
Article history
Received:
October 18 2012
Citation
Mathilde Chivet, Charlotte Javalet, Fiona Hemming, Karin Pernet-Gallay, Karine Laulagnier, Sandrine Fraboulet, Rémy Sadoul; Exosomes as a novel way of interneuronal communication. Biochem Soc Trans 1 February 2013; 41 (1): 241–244. doi: https://doi.org/10.1042/BST20120266
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