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Isolation of microglia-derived extracellular vesicles: towards miRNA signatures and neuroprotection.
J Nanobiotechnology. 2019 Dec 04; 17(1):119.JN

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.

Authors+Show Affiliations

Laboratoire de Protéomique, Réponse Inflammatoire Et Spectrométrie de Masse (PRISM), INSERM U1192, Université de Lille, 59000, Lille, France.Laboratoire de Protéomique, Réponse Inflammatoire Et Spectrométrie de Masse (PRISM), INSERM U1192, Université de Lille, 59000, Lille, France.Laboratoire de Protéomique, Réponse Inflammatoire Et Spectrométrie de Masse (PRISM), INSERM U1192, Université de Lille, 59000, Lille, France.Laboratoire de Protéomique, Réponse Inflammatoire Et Spectrométrie de Masse (PRISM), INSERM U1192, Université de Lille, 59000, Lille, France.Department of Biomedical and Biotechnological Sciences, Section of Pharmacology, University of Catania, Catania, Italy.IOM Ricerca Srl, Catania, Italy.Laboratoire de Protéomique, Réponse Inflammatoire Et Spectrométrie de Masse (PRISM), INSERM U1192, Université de Lille, 59000, Lille, France.Centre de Recherche Jean-Pierre AUBERT (JPArc), INSERM U1172, Université de Lille, 59000, Lille, France.Centre de Recherche Jean-Pierre AUBERT (JPArc), INSERM U1172, Université de Lille, 59000, Lille, France.Laboratoire de Protéomique, Réponse Inflammatoire Et Spectrométrie de Masse (PRISM), INSERM U1192, Université de Lille, 59000, Lille, France.Laboratoire de Protéomique, Réponse Inflammatoire Et Spectrométrie de Masse (PRISM), INSERM U1192, Université de Lille, 59000, Lille, France.Laboratoire de Protéomique, Réponse Inflammatoire Et Spectrométrie de Masse (PRISM), INSERM U1192, Université de Lille, 59000, Lille, France.Laboratoire de Protéomique, Réponse Inflammatoire Et Spectrométrie de Masse (PRISM), INSERM U1192, Université de Lille, 59000, Lille, France. christophe.lefebvre@univ-lille.fr.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

31801555

Citation

Lemaire, Quentin, et al. "Isolation of Microglia-derived Extracellular Vesicles: Towards miRNA Signatures and Neuroprotection." Journal of Nanobiotechnology, vol. 17, no. 1, 2019, p. 119.
Lemaire Q, Raffo-Romero A, Arab T, et al. Isolation of microglia-derived extracellular vesicles: towards miRNA signatures and neuroprotection. J Nanobiotechnology. 2019;17(1):119.
Lemaire, Q., Raffo-Romero, A., Arab, T., Van Camp, C., Drago, F., Forte, S., Gimeno, J. P., Begard, S., Colin, M., Vizioli, J., Sautière, P. E., Salzet, M., & Lefebvre, C. (2019). Isolation of microglia-derived extracellular vesicles: towards miRNA signatures and neuroprotection. Journal of Nanobiotechnology, 17(1), 119. https://doi.org/10.1186/s12951-019-0551-6
Lemaire Q, et al. Isolation of Microglia-derived Extracellular Vesicles: Towards miRNA Signatures and Neuroprotection. J Nanobiotechnology. 2019 Dec 4;17(1):119. PubMed PMID: 31801555.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Isolation of microglia-derived extracellular vesicles: towards miRNA signatures and neuroprotection. AU - Lemaire,Quentin, AU - Raffo-Romero,Antonella, AU - Arab,Tanina, AU - Van Camp,Christelle, AU - Drago,Francesco, AU - Forte,Stefano, AU - Gimeno,Jean-Pascal, AU - Begard,Séverine, AU - Colin,Morvane, AU - Vizioli,Jacopo, AU - Sautière,Pierre-Eric, AU - Salzet,Michel, AU - Lefebvre,Christophe, Y1 - 2019/12/04/ PY - 2019/09/09/received PY - 2019/11/20/accepted PY - 2019/12/6/entrez PY - 2019/12/6/pubmed PY - 2020/4/23/medline KW - Extracellular vesicles KW - Leech Hirudo medicinalis KW - Microglia KW - Neuroprotection KW - miRNAs SP - 119 EP - 119 JF - Journal of nanobiotechnology JO - J Nanobiotechnology VL - 17 IS - 1 N2 - 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. SN - 1477-3155 UR - https://www.unboundmedicine.com/medline/citation/31801555/Isolation_of_microglia_derived_extracellular_vesicles:_towards_miRNA_signatures_and_neuroprotection_ DB - PRIME DP - Unbound Medicine ER -