4.7 Review

Exosome Circuitry During (De)(Re)Myelination of the Central Nervous System

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2020.00483

Keywords

Exosomes; myelin; axon-oligodendrocyte unit; demyelinating diseases; biomarkers; therapeutic vehicles; mesenchymal stem cells; secretome

Funding

  1. Premios Santa Casa Neurociencias -Prize Melo e Castro for Spinal Cord Injury Research [MC-04/17]
  2. Prize Mantero Belard for Neurodegenerative Diseases Research [MB-28-2019]
  3. European Regional Development Fund (FEDER), through the Foundation for Science and Technology (FCT) [POCI-01-0145-FEDER-007038, TUBITAK/0007/2014, PTDC/DTP-FTO/5109/2014, POCI-01-0145-FEDER-029206, POCI-01-0145-FEDER-031392, PTDC/MED-NEU/31417/2017]
  4. Northern Portugal Regional Operational Programme (NORTE 2020), under the Portugal 2020 Partnership Agreement, through FEDER [NORTE01-0145-FEDER-000013, NORTE-01-0145-FEDER-000023]
  5. La Caixa Foundation [100010434, LCF/BQ/PI19/11690005]
  6. [NORTE-01-0145-FEDER-029968]
  7. [POCI-01-0145-FEDER029751]
  8. [POCI-01-0145-FEDER-032619]
  9. Fundação para a Ciência e a Tecnologia [PTDC/DTP-FTO/5109/2014] Funding Source: FCT

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Reciprocal neuron-glia cell communication is fundamental for the proper function of the nervous system. Oligodendrocytes are the myelinating cells of the central nervous system (CNS) that insulate and provide trophic support to neurons. This effective interaction is crucial not only for myelination but also for long-term axonal survival and neural connectivity. In recent years, exosomes have been portrayed as key players in intercellular interaction in the context of the healthy and diseased CNS. They act as communicating vehicles, true attaches operating between neurons and glial cells. Despite the complex exosome circuitry within the nervous system, experimental evidence supports the role of exosomes in modulating myelination. Oligodendrocytes secrete exosomes in response to neuronal signals in an electric activity-dependent manner. These released exosomes are then internalized by neurons, contributing to their integrity and activity. In turn, neurons secrete exosomes to control the communication between them and with myelinating cells in order to regulate synaptic function in neuronal development, myelin maintenance, and neuroregeneration. In this review, we provide a critical view of the current understanding on how exosomes, either from CNS-resident cells or from the periphery, contribute to the formation and maintenance of myelin and, additionally, on how the differential content of exosomes in normal and pathological conditions foresees the use of these nanovesicles as putative diagnostic and/or therapeutical agents in white matter degeneration-associated diseases.

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