Microglial microvesicles secretion and intercellular signalling

Microvesicles (MVs) are released from almost all cell brain types into the microenvironment and are emerging as a novel way of cell-to-cell communication. This review focuses on MVs discharged by microglial cells, the brain resident myeloid cells, which comprise approximately 10-12% of brain populat...

Full description

Bibliographic Details
Main Authors: Elena eTurola, Roberto eFurlan, Fabio eBianco, Michela eMatteoli, Claudia eVerderio
Format: Article
Language:English
Published: Frontiers Media S.A. 2012-05-01
Series:Frontiers in Physiology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fphys.2012.00149/full
id doaj-e9fe189b5b734986a46f078a79895657
record_format Article
spelling doaj-e9fe189b5b734986a46f078a798956572020-11-24T23:05:57ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2012-05-01310.3389/fphys.2012.0014923973Microglial microvesicles secretion and intercellular signallingElena eTurola0Elena eTurola1Roberto eFurlan2Fabio eBianco3Michela eMatteoli4Michela eMatteoli5Michela eMatteoli6Claudia eVerderio7Claudia eVerderio8CNR Institute of NeuroscienceUniversity of MilanFondazione San Raffaele del monte TaborNeuro-zone.srlCNR Institute of NeuroscienceUniversity of MilanIstituto Clinico IRCCS HumanitasCNR Institute of NeuroscienceUniversity of MilanMicrovesicles (MVs) are released from almost all cell brain types into the microenvironment and are emerging as a novel way of cell-to-cell communication. This review focuses on MVs discharged by microglial cells, the brain resident myeloid cells, which comprise approximately 10-12% of brain population. In this review, we summarize first evidence indicating that MV shedding is a process activated by the ATP receptor P2X7 and that shed MVs represent a secretory pathway for the inflammatory cytokine IL-1beta We then discuss subsequent findings which clarify how IL-1beta can be locally processed and released from MVs into the extracellular environment. In addition, we describe the current understanding about the mechanism of P2X7-dependent MV formation and membrane abscission, which, by involving sphingomyelinase activity and ceramide formation, may share similarities with exosome biogenesis. Finally we report our recent results which show that MVs can stimulate neuronal activity, and suggest new areas for future investigationhttp://journal.frontiersin.org/Journal/10.3389/fphys.2012.00149/fullMicrovesiclesMicroglial cellsIL-betaNeuronal activityBrain inflammation
collection DOAJ
language English
format Article
sources DOAJ
author Elena eTurola
Elena eTurola
Roberto eFurlan
Fabio eBianco
Michela eMatteoli
Michela eMatteoli
Michela eMatteoli
Claudia eVerderio
Claudia eVerderio
spellingShingle Elena eTurola
Elena eTurola
Roberto eFurlan
Fabio eBianco
Michela eMatteoli
Michela eMatteoli
Michela eMatteoli
Claudia eVerderio
Claudia eVerderio
Microglial microvesicles secretion and intercellular signalling
Frontiers in Physiology
Microvesicles
Microglial cells
IL-beta
Neuronal activity
Brain inflammation
author_facet Elena eTurola
Elena eTurola
Roberto eFurlan
Fabio eBianco
Michela eMatteoli
Michela eMatteoli
Michela eMatteoli
Claudia eVerderio
Claudia eVerderio
author_sort Elena eTurola
title Microglial microvesicles secretion and intercellular signalling
title_short Microglial microvesicles secretion and intercellular signalling
title_full Microglial microvesicles secretion and intercellular signalling
title_fullStr Microglial microvesicles secretion and intercellular signalling
title_full_unstemmed Microglial microvesicles secretion and intercellular signalling
title_sort microglial microvesicles secretion and intercellular signalling
publisher Frontiers Media S.A.
series Frontiers in Physiology
issn 1664-042X
publishDate 2012-05-01
description Microvesicles (MVs) are released from almost all cell brain types into the microenvironment and are emerging as a novel way of cell-to-cell communication. This review focuses on MVs discharged by microglial cells, the brain resident myeloid cells, which comprise approximately 10-12% of brain population. In this review, we summarize first evidence indicating that MV shedding is a process activated by the ATP receptor P2X7 and that shed MVs represent a secretory pathway for the inflammatory cytokine IL-1beta We then discuss subsequent findings which clarify how IL-1beta can be locally processed and released from MVs into the extracellular environment. In addition, we describe the current understanding about the mechanism of P2X7-dependent MV formation and membrane abscission, which, by involving sphingomyelinase activity and ceramide formation, may share similarities with exosome biogenesis. Finally we report our recent results which show that MVs can stimulate neuronal activity, and suggest new areas for future investigation
topic Microvesicles
Microglial cells
IL-beta
Neuronal activity
Brain inflammation
url http://journal.frontiersin.org/Journal/10.3389/fphys.2012.00149/full
work_keys_str_mv AT elenaeturola microglialmicrovesiclessecretionandintercellularsignalling
AT elenaeturola microglialmicrovesiclessecretionandintercellularsignalling
AT robertoefurlan microglialmicrovesiclessecretionandintercellularsignalling
AT fabioebianco microglialmicrovesiclessecretionandintercellularsignalling
AT michelaematteoli microglialmicrovesiclessecretionandintercellularsignalling
AT michelaematteoli microglialmicrovesiclessecretionandintercellularsignalling
AT michelaematteoli microglialmicrovesiclessecretionandintercellularsignalling
AT claudiaeverderio microglialmicrovesiclessecretionandintercellularsignalling
AT claudiaeverderio microglialmicrovesiclessecretionandintercellularsignalling
_version_ 1725624673608138752