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Diurnal Variation of Plasma Extracellular Vesicle Is Disrupted in People Living with HIV
Background: Several types of extracellular vesicles (EVs) secreted by various immune and non-immune cells are present in the human plasma. We previously demonstrated that EV abundance and microRNA content change in pathological conditions, such as HIV infection. Here, we investigated daily variation...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8145918/ https://www.ncbi.nlm.nih.gov/pubmed/33923310 http://dx.doi.org/10.3390/pathogens10050518 |
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author | Bazié, Wilfried Wenceslas Goyer, Benjamin Boucher, Julien Zhang, Yuwei Planas, Delphine Chatterjee, Debashree Routy, Jean-Pierre Alary, Michel Ancuta, Petronela Gilbert, Caroline |
author_facet | Bazié, Wilfried Wenceslas Goyer, Benjamin Boucher, Julien Zhang, Yuwei Planas, Delphine Chatterjee, Debashree Routy, Jean-Pierre Alary, Michel Ancuta, Petronela Gilbert, Caroline |
author_sort | Bazié, Wilfried Wenceslas |
collection | PubMed |
description | Background: Several types of extracellular vesicles (EVs) secreted by various immune and non-immune cells are present in the human plasma. We previously demonstrated that EV abundance and microRNA content change in pathological conditions, such as HIV infection. Here, we investigated daily variations of large and small EVs, in terms of abundance and microRNA contents in people living with HIV (PLWH) receiving antiretroviral therapy (HIV+ART) and uninfected controls (HIV−). Methods: Venous blood samples from n = 10 HIV+ART and n = 10 HIV− participants were collected at 10:00 and 22:00 the same day. Large and small plasma EVs were purified, counted, and the mature miRNAs miR-29a, miR-29b, miR-92, miR-155, and miR-223 copies were measured by RT-PCR. Results: Large EVs were significantly bigger in the plasma collected at 10:00 versus 22:00 in both groups. There was a significant day–night increase in the quantity of 5 miRNAs in HIV− large EVs. In HIV+ART, only miR-155 daily variation has been observed in large EVs. Finally, EV-miRNA content permits to distinguish HIV− to HIV+ART in multivariate analysis. Conclusion: These results point that plasma EV amount and microRNA contents are under daily variation in HIV− people. This new dynamic measure is disrupted in PLWH despite viral-suppressive ART. This study highlights a significant difference concerning EV abundance and their content measured at 22:00 between both groups. Therefore, the time of blood collection must be considered in the future for the EV as biomarkers. |
format | Online Article Text |
id | pubmed-8145918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-81459182021-05-26 Diurnal Variation of Plasma Extracellular Vesicle Is Disrupted in People Living with HIV Bazié, Wilfried Wenceslas Goyer, Benjamin Boucher, Julien Zhang, Yuwei Planas, Delphine Chatterjee, Debashree Routy, Jean-Pierre Alary, Michel Ancuta, Petronela Gilbert, Caroline Pathogens Article Background: Several types of extracellular vesicles (EVs) secreted by various immune and non-immune cells are present in the human plasma. We previously demonstrated that EV abundance and microRNA content change in pathological conditions, such as HIV infection. Here, we investigated daily variations of large and small EVs, in terms of abundance and microRNA contents in people living with HIV (PLWH) receiving antiretroviral therapy (HIV+ART) and uninfected controls (HIV−). Methods: Venous blood samples from n = 10 HIV+ART and n = 10 HIV− participants were collected at 10:00 and 22:00 the same day. Large and small plasma EVs were purified, counted, and the mature miRNAs miR-29a, miR-29b, miR-92, miR-155, and miR-223 copies were measured by RT-PCR. Results: Large EVs were significantly bigger in the plasma collected at 10:00 versus 22:00 in both groups. There was a significant day–night increase in the quantity of 5 miRNAs in HIV− large EVs. In HIV+ART, only miR-155 daily variation has been observed in large EVs. Finally, EV-miRNA content permits to distinguish HIV− to HIV+ART in multivariate analysis. Conclusion: These results point that plasma EV amount and microRNA contents are under daily variation in HIV− people. This new dynamic measure is disrupted in PLWH despite viral-suppressive ART. This study highlights a significant difference concerning EV abundance and their content measured at 22:00 between both groups. Therefore, the time of blood collection must be considered in the future for the EV as biomarkers. MDPI 2021-04-24 /pmc/articles/PMC8145918/ /pubmed/33923310 http://dx.doi.org/10.3390/pathogens10050518 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bazié, Wilfried Wenceslas Goyer, Benjamin Boucher, Julien Zhang, Yuwei Planas, Delphine Chatterjee, Debashree Routy, Jean-Pierre Alary, Michel Ancuta, Petronela Gilbert, Caroline Diurnal Variation of Plasma Extracellular Vesicle Is Disrupted in People Living with HIV |
title | Diurnal Variation of Plasma Extracellular Vesicle Is Disrupted in People Living with HIV |
title_full | Diurnal Variation of Plasma Extracellular Vesicle Is Disrupted in People Living with HIV |
title_fullStr | Diurnal Variation of Plasma Extracellular Vesicle Is Disrupted in People Living with HIV |
title_full_unstemmed | Diurnal Variation of Plasma Extracellular Vesicle Is Disrupted in People Living with HIV |
title_short | Diurnal Variation of Plasma Extracellular Vesicle Is Disrupted in People Living with HIV |
title_sort | diurnal variation of plasma extracellular vesicle is disrupted in people living with hiv |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8145918/ https://www.ncbi.nlm.nih.gov/pubmed/33923310 http://dx.doi.org/10.3390/pathogens10050518 |
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