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Immune and central nervous system-related miRNAs expression profiling in monocytes of multiple sclerosis patients

It is widely recognized that monocytes-macrophages adopt a wide variety of phenotypes, influencing the inflammatory activity and demyelination in Multiple Sclerosis (MS). However, how the phenotype of human monocytes evolves in the course of MS is largely unknown. The aim of our preliminary study wa...

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Autores principales: Amoruso, Antonella, Blonda, Maria, Gironi, Maira, Grasso, Roberta, Di Francescantonio, Valeria, Scaroni, Federica, Furlan, Roberto, Verderio, Claudia, Avolio, Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145856/
https://www.ncbi.nlm.nih.gov/pubmed/32273558
http://dx.doi.org/10.1038/s41598-020-63282-3
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author Amoruso, Antonella
Blonda, Maria
Gironi, Maira
Grasso, Roberta
Di Francescantonio, Valeria
Scaroni, Federica
Furlan, Roberto
Verderio, Claudia
Avolio, Carlo
author_facet Amoruso, Antonella
Blonda, Maria
Gironi, Maira
Grasso, Roberta
Di Francescantonio, Valeria
Scaroni, Federica
Furlan, Roberto
Verderio, Claudia
Avolio, Carlo
author_sort Amoruso, Antonella
collection PubMed
description It is widely recognized that monocytes-macrophages adopt a wide variety of phenotypes, influencing the inflammatory activity and demyelination in Multiple Sclerosis (MS). However, how the phenotype of human monocytes evolves in the course of MS is largely unknown. The aim of our preliminary study was to analyse in monocytes of relapsing-remitting and progressive forms of MS patients the expression of a set of miRNAs which impact monocyte-macrophage immune function and their communication with brain cells. Quantitative PCR showed that miRNAs with anti-inflammatory functions, which promote pro-regenerative polarization, are increased in MS patients, while pro-inflammatory miR-155 is downregulated in the same patients. These changes may indicate the attempt of monocytes to counteract neuroinflammation. miR-124, an anti-inflammatory marker but also of myeloid cell quiescence was strongly downregulated, especially in progressive MS patients, suggesting complete loss of homeostatic monocyte function in the progressive disease phase. Profiling of miRNAs that control monocyte polarization may help to define not only the activation state of monocytes in the course of the disease but also novel pathogenic mechanisms.
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spelling pubmed-71458562020-04-15 Immune and central nervous system-related miRNAs expression profiling in monocytes of multiple sclerosis patients Amoruso, Antonella Blonda, Maria Gironi, Maira Grasso, Roberta Di Francescantonio, Valeria Scaroni, Federica Furlan, Roberto Verderio, Claudia Avolio, Carlo Sci Rep Article It is widely recognized that monocytes-macrophages adopt a wide variety of phenotypes, influencing the inflammatory activity and demyelination in Multiple Sclerosis (MS). However, how the phenotype of human monocytes evolves in the course of MS is largely unknown. The aim of our preliminary study was to analyse in monocytes of relapsing-remitting and progressive forms of MS patients the expression of a set of miRNAs which impact monocyte-macrophage immune function and their communication with brain cells. Quantitative PCR showed that miRNAs with anti-inflammatory functions, which promote pro-regenerative polarization, are increased in MS patients, while pro-inflammatory miR-155 is downregulated in the same patients. These changes may indicate the attempt of monocytes to counteract neuroinflammation. miR-124, an anti-inflammatory marker but also of myeloid cell quiescence was strongly downregulated, especially in progressive MS patients, suggesting complete loss of homeostatic monocyte function in the progressive disease phase. Profiling of miRNAs that control monocyte polarization may help to define not only the activation state of monocytes in the course of the disease but also novel pathogenic mechanisms. Nature Publishing Group UK 2020-04-09 /pmc/articles/PMC7145856/ /pubmed/32273558 http://dx.doi.org/10.1038/s41598-020-63282-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Amoruso, Antonella
Blonda, Maria
Gironi, Maira
Grasso, Roberta
Di Francescantonio, Valeria
Scaroni, Federica
Furlan, Roberto
Verderio, Claudia
Avolio, Carlo
Immune and central nervous system-related miRNAs expression profiling in monocytes of multiple sclerosis patients
title Immune and central nervous system-related miRNAs expression profiling in monocytes of multiple sclerosis patients
title_full Immune and central nervous system-related miRNAs expression profiling in monocytes of multiple sclerosis patients
title_fullStr Immune and central nervous system-related miRNAs expression profiling in monocytes of multiple sclerosis patients
title_full_unstemmed Immune and central nervous system-related miRNAs expression profiling in monocytes of multiple sclerosis patients
title_short Immune and central nervous system-related miRNAs expression profiling in monocytes of multiple sclerosis patients
title_sort immune and central nervous system-related mirnas expression profiling in monocytes of multiple sclerosis patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145856/
https://www.ncbi.nlm.nih.gov/pubmed/32273558
http://dx.doi.org/10.1038/s41598-020-63282-3
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