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Isolation of microglia-derived extracellular vesicles: towards miRNA signatures and neuroprotection

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 t...

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Autores principales: Lemaire, Quentin, Raffo-Romero, Antonella, Arab, Tanina, Van Camp, Christelle, Drago, Francesco, Forte, Stefano, Gimeno, Jean-Pascal, Begard, Séverine, Colin, Morvane, Vizioli, Jacopo, Sautière, Pierre-Eric, Salzet, Michel, Lefebvre, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894150/
https://www.ncbi.nlm.nih.gov/pubmed/31801555
http://dx.doi.org/10.1186/s12951-019-0551-6
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author Lemaire, Quentin
Raffo-Romero, Antonella
Arab, Tanina
Van Camp, Christelle
Drago, Francesco
Forte, Stefano
Gimeno, Jean-Pascal
Begard, Séverine
Colin, Morvane
Vizioli, Jacopo
Sautière, Pierre-Eric
Salzet, Michel
Lefebvre, Christophe
author_facet Lemaire, Quentin
Raffo-Romero, Antonella
Arab, Tanina
Van Camp, Christelle
Drago, Francesco
Forte, Stefano
Gimeno, Jean-Pascal
Begard, Séverine
Colin, Morvane
Vizioli, Jacopo
Sautière, Pierre-Eric
Salzet, Michel
Lefebvre, Christophe
author_sort Lemaire, Quentin
collection PubMed
description 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.
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spelling pubmed-68941502019-12-11 Isolation of microglia-derived extracellular vesicles: towards miRNA signatures and neuroprotection Lemaire, Quentin Raffo-Romero, Antonella Arab, Tanina Van Camp, Christelle Drago, Francesco Forte, Stefano Gimeno, Jean-Pascal Begard, Séverine Colin, Morvane Vizioli, Jacopo Sautière, Pierre-Eric Salzet, Michel Lefebvre, Christophe J Nanobiotechnology Research 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. BioMed Central 2019-12-04 /pmc/articles/PMC6894150/ /pubmed/31801555 http://dx.doi.org/10.1186/s12951-019-0551-6 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lemaire, Quentin
Raffo-Romero, Antonella
Arab, Tanina
Van Camp, Christelle
Drago, Francesco
Forte, Stefano
Gimeno, Jean-Pascal
Begard, Séverine
Colin, Morvane
Vizioli, Jacopo
Sautière, Pierre-Eric
Salzet, Michel
Lefebvre, Christophe
Isolation of microglia-derived extracellular vesicles: towards miRNA signatures and neuroprotection
title Isolation of microglia-derived extracellular vesicles: towards miRNA signatures and neuroprotection
title_full Isolation of microglia-derived extracellular vesicles: towards miRNA signatures and neuroprotection
title_fullStr Isolation of microglia-derived extracellular vesicles: towards miRNA signatures and neuroprotection
title_full_unstemmed Isolation of microglia-derived extracellular vesicles: towards miRNA signatures and neuroprotection
title_short Isolation of microglia-derived extracellular vesicles: towards miRNA signatures and neuroprotection
title_sort isolation of microglia-derived extracellular vesicles: towards mirna signatures and neuroprotection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894150/
https://www.ncbi.nlm.nih.gov/pubmed/31801555
http://dx.doi.org/10.1186/s12951-019-0551-6
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