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Characterization of Immune Cell-derived Extracellular Vesicles and Studying Functional Impact on Cell Environment
Published on: June 2, 2020
Isolation of microglia-derived extracellular vesicles: towards miRNA signatures and neuroprotection
Quentin Lemaire1, Antonella Raffo-Romero1, Tanina Arab1
1Laboratoire de Protéomique, Réponse Inflammatoire Et Spectrométrie de Masse (PRISM), INSERM U1192, Université de Lille, 59000, Lille, France.
Abstract:
The functional preservation of the central nervous system (CNS) is based on the neuronal plasticity and survival. In this context, the neuroinflammatory state plays a key role and involves the microglial cells, the CNS-resident macrophages. In order to better understand the microglial contribution to the neuroprotection, microglia-derived extracellular vesicles (EVs) were isolated and molecularly characterized to be then studied in neurite outgrowth assays. The EVs, mainly composed of exosomes and microparticles, are an important cell-to-cell communication process as they exhibit different types of mediators (proteins, lipids, nucleic acids) to recipient cells. The medicinal leech CNS was initially used as an interesting model of microglia/neuron crosstalk due to their easy collection for primary cultures. After the microglia-derived EV isolation following successive methods, we developed their large-scale and non-targeted proteomic analysis to (i) detect as many EV protein markers as possible, (ii) better understand the biologically active proteins in EVs and (iii) evaluate the resulting protein signatures in EV-activated neurons. The EV functional properties were also evaluated in neurite outgrowth assays on rat primary neurons and the RNAseq analysis of the microglia-derived EVs was performed to propose the most representative miRNAs in microglia-derived EVs. This strategy allowed validating the EV isolation, identify major biological pathways in EVs and corroborate the regenerative process in EV-activated neurons. In parallel, six different miRNAs were originally identified in microglia-derived EVs including 3 which were only known in plants until now. The analysis of the neuronal proteins under the microglial EV activation suggested possible miRNA-dependent regulation mechanisms. Taken together, this combination of methodologies showed the leech microglial EVs as neuroprotective cargos across species and contributed to propose original EV-associated miRNAs whose functions will have to be evaluated in the EV-dependent dialog between microglia and neurons.
Insights
Leech microglial extracellular vesicles (EVs) demonstrate neuroprotective properties by promoting neuronal survival and regeneration. These EVs contain novel microRNAs (miRNAs) that may mediate cross-species communication, highlighting their therapeutic potential.
Area of Science:
- Neuroscience
- Cell Biology
- Extracellular Vesicles
Background:
- Central nervous system (CNS) preservation relies on neuronal plasticity and survival.
- Neuroinflammation, involving microglial cells, critically influences CNS health.
- Microglia-derived extracellular vesicles (EVs) are key mediators of cell-to-cell communication.
Purpose of the Study:
- To investigate the neuroprotective role of microglia-derived EVs.
- To characterize the molecular cargo of EVs for understanding their function.
- To assess the impact of EVs on neuronal outgrowth and regeneration.
Main Methods:
- Isolation and molecular characterization of microglia-derived EVs.
- Large-scale, non-targeted proteomic and RNA sequencing (RNAseq) analysis of EVs.
- Neurite outgrowth assays using primary rat neurons.
Main Results:
- Validated EV isolation and identified major biological pathways.
- Corroborated regenerative processes in EV-activated neurons.
- Identified six novel microRNAs (miRNAs) in EVs, including three previously unknown in animals.
Conclusions:
- Medicinal leech microglial EVs act as cross-species neuroprotective cargos.
- Original EV-associated miRNAs were identified, suggesting potential regulatory roles in neuroprotection.
- Further research is needed to elucidate the function of these miRNAs in microglia-neuron communication.

