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Microglia-Derived Microvesicles Affect Microglia Phenotype in Glioma
Extracellular-released vesicles (EVs), such as microvesicles (MV) and exosomes (Exo) provide a new type of inter-cellular communication, directly transferring a ready to use box of information, consisting of proteins, lipids and nucleic acids. In the nervous system, EVs participate to neuron-glial c...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395438/ https://www.ncbi.nlm.nih.gov/pubmed/30853898 http://dx.doi.org/10.3389/fncel.2019.00041 |
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author | Grimaldi, Alfonso Serpe, Carmela Chece, Giuseppina Nigro, Valentina Sarra, Angelo Ruzicka, Barbara Relucenti, Michela Familiari, Giuseppe Ruocco, Giancarlo Pascucci, Giuseppe Rubens Guerrieri, Francesca Limatola, Cristina Catalano, Myriam |
author_facet | Grimaldi, Alfonso Serpe, Carmela Chece, Giuseppina Nigro, Valentina Sarra, Angelo Ruzicka, Barbara Relucenti, Michela Familiari, Giuseppe Ruocco, Giancarlo Pascucci, Giuseppe Rubens Guerrieri, Francesca Limatola, Cristina Catalano, Myriam |
author_sort | Grimaldi, Alfonso |
collection | PubMed |
description | Extracellular-released vesicles (EVs), such as microvesicles (MV) and exosomes (Exo) provide a new type of inter-cellular communication, directly transferring a ready to use box of information, consisting of proteins, lipids and nucleic acids. In the nervous system, EVs participate to neuron-glial cross-talk, a bidirectional communication important to preserve brain homeostasis and, when dysfunctional, involved in several CNS diseases. We investigated whether microglia-derived EVs could be used to transfer a protective phenotype to dysfunctional microglia in the context of a brain tumor. When MV, isolated from microglia stimulated with LPS/IFNγ were brain injected in glioma-bearing mice, we observed a phenotype switch of tumor associated myeloid cells (TAMs) and a reduction of tumor size. Our findings indicate that the MV cargo, which contains upregulated transcripts for several inflammation-related genes, can transfer information in the brain of glioma bearing mice modifying microglial gene expression, reducing neuronal death and glioma invasion, thus promoting the recovery of brain homeostasis. |
format | Online Article Text |
id | pubmed-6395438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63954382019-03-08 Microglia-Derived Microvesicles Affect Microglia Phenotype in Glioma Grimaldi, Alfonso Serpe, Carmela Chece, Giuseppina Nigro, Valentina Sarra, Angelo Ruzicka, Barbara Relucenti, Michela Familiari, Giuseppe Ruocco, Giancarlo Pascucci, Giuseppe Rubens Guerrieri, Francesca Limatola, Cristina Catalano, Myriam Front Cell Neurosci Neuroscience Extracellular-released vesicles (EVs), such as microvesicles (MV) and exosomes (Exo) provide a new type of inter-cellular communication, directly transferring a ready to use box of information, consisting of proteins, lipids and nucleic acids. In the nervous system, EVs participate to neuron-glial cross-talk, a bidirectional communication important to preserve brain homeostasis and, when dysfunctional, involved in several CNS diseases. We investigated whether microglia-derived EVs could be used to transfer a protective phenotype to dysfunctional microglia in the context of a brain tumor. When MV, isolated from microglia stimulated with LPS/IFNγ were brain injected in glioma-bearing mice, we observed a phenotype switch of tumor associated myeloid cells (TAMs) and a reduction of tumor size. Our findings indicate that the MV cargo, which contains upregulated transcripts for several inflammation-related genes, can transfer information in the brain of glioma bearing mice modifying microglial gene expression, reducing neuronal death and glioma invasion, thus promoting the recovery of brain homeostasis. Frontiers Media S.A. 2019-02-22 /pmc/articles/PMC6395438/ /pubmed/30853898 http://dx.doi.org/10.3389/fncel.2019.00041 Text en Copyright © 2019 Grimaldi, Serpe, Chece, Nigro, Sarra, Ruzicka, Relucenti, Familiari, Ruocco, Pascucci, Guerrieri, Limatola and Catalano. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Grimaldi, Alfonso Serpe, Carmela Chece, Giuseppina Nigro, Valentina Sarra, Angelo Ruzicka, Barbara Relucenti, Michela Familiari, Giuseppe Ruocco, Giancarlo Pascucci, Giuseppe Rubens Guerrieri, Francesca Limatola, Cristina Catalano, Myriam Microglia-Derived Microvesicles Affect Microglia Phenotype in Glioma |
title | Microglia-Derived Microvesicles Affect Microglia Phenotype in Glioma |
title_full | Microglia-Derived Microvesicles Affect Microglia Phenotype in Glioma |
title_fullStr | Microglia-Derived Microvesicles Affect Microglia Phenotype in Glioma |
title_full_unstemmed | Microglia-Derived Microvesicles Affect Microglia Phenotype in Glioma |
title_short | Microglia-Derived Microvesicles Affect Microglia Phenotype in Glioma |
title_sort | microglia-derived microvesicles affect microglia phenotype in glioma |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395438/ https://www.ncbi.nlm.nih.gov/pubmed/30853898 http://dx.doi.org/10.3389/fncel.2019.00041 |
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