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Updated: May 21, 2026

Characterization of Immune Cell-derived Extracellular Vesicles and Studying Functional Impact on Cell Environment
Published on: June 2, 2020
Microglial microvesicle secretion and intercellular signaling
Elena Turola1, Roberto Furlan, Fabio Bianco
1CNR Institute of Neuroscience Milano, Italy.
Abstract:
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 ∼10-12% of brain population. We summarize first evidence indicating that MV shedding is a process activated by the ATP receptor P2X(7) and that shed MVs represent a secretory pathway for the inflammatory cytokine IL-β. We then discuss subsequent findings which clarify how IL-1 β can be locally processed and released from MVs into the extracellular environment. In addition, we describe the current understanding about the mechanism of P2X(7)-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 microglia-derived MVs can stimulate neuronal activity and participate to the propagation of inflammatory signals, and suggest new areas for future investigation.
Insights
Microglia release microvesicles (MVs) that carry inflammatory IL-1β, acting as a communication pathway. These MVs stimulate neuronal activity and spread inflammation in the brain.
Area of Science:
- Neuroscience
- Cell Biology
- Immunology
Background:
- Microvesicles (MVs) are key mediators of intercellular communication in the brain.
- Microglia, the resident immune cells of the brain, release MVs involved in neuroinflammation.
- The P2X7 receptor (P2X7R) plays a crucial role in MV shedding from various cell types.
Purpose of the Study:
- To review the role of microglial MVs in cell-to-cell communication.
- To elucidate the mechanisms of P2X7R-dependent MV formation and IL-1β release.
- To highlight the impact of microglia-derived MVs on neuronal activity and inflammatory signaling.
Main Methods:
- Review of existing literature on microvesicle shedding and P2X7R signaling.
- Analysis of studies investigating IL-1β processing and release via MVs.
- Examination of research on microglia-MV interactions with neurons.
Main Results:
- MV shedding from microglia is activated by the P2X7 receptor.
- Microglia-derived MVs serve as a secretory pathway for the inflammatory cytokine IL-1β.
- P2X7-dependent MV formation involves sphingomyelinase activity and ceramide production, potentially similar to exosome biogenesis.
- Microglia-derived MVs can enhance neuronal activity and propagate inflammatory signals.
Conclusions:
- Microglia-derived MVs are significant players in brain communication and neuroinflammation.
- The P2X7 receptor is central to the release and function of these inflammatory MVs.
- Further research into microglia-derived MVs could reveal new therapeutic targets for neurological disorders.
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