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Affinity enrichment of extracellular vesicles from plasma reveals mRNA changes associated with acute ischemic stroke
Currently there is no in vitro diagnostic test for acute ischemic stroke (AIS), yet rapid diagnosis is crucial for effective thrombolytic treatment. We previously demonstrated the utility of CD8(+) T-cells’ mRNA expression for AIS detection; however extracellular vesicles (EVs) were not evaluated as...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589468/ https://www.ncbi.nlm.nih.gov/pubmed/33106557 http://dx.doi.org/10.1038/s42003-020-01336-y |
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author | Wijerathne, Harshani Witek, Malgorzata A. Jackson, Joshua M. Brown, Virginia Hupert, Mateusz L. Herrera, Kristina Kramer, Cameron Davidow, Abigail E. Li, Yan Baird, Alison E. Murphy, Michael C. Soper, Steven A. |
author_facet | Wijerathne, Harshani Witek, Malgorzata A. Jackson, Joshua M. Brown, Virginia Hupert, Mateusz L. Herrera, Kristina Kramer, Cameron Davidow, Abigail E. Li, Yan Baird, Alison E. Murphy, Michael C. Soper, Steven A. |
author_sort | Wijerathne, Harshani |
collection | PubMed |
description | Currently there is no in vitro diagnostic test for acute ischemic stroke (AIS), yet rapid diagnosis is crucial for effective thrombolytic treatment. We previously demonstrated the utility of CD8(+) T-cells’ mRNA expression for AIS detection; however extracellular vesicles (EVs) were not evaluated as a source of mRNA for AIS testing. We now report a microfluidic device for the rapid and efficient affinity-enrichment of CD8(+) EVs and subsequent EV’s mRNA analysis using droplet digital PCR (ddPCR). The microfluidic device contains a dense array of micropillars modified with anti-CD8α monoclonal antibodies that enriched 158 ± 10 nm sized EVs at 4.3 ± 2.1 × 10(9) particles/100 µL of plasma. Analysis of mRNA from CD8(+) EVs and their parental T-cells revealed correlation in the expression for AIS-specific genes in both cell lines and healthy donors. In a blinded study, 80% test positivity for AIS patients and controls was revealed with a total analysis time of 3.7 h. |
format | Online Article Text |
id | pubmed-7589468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75894682020-10-29 Affinity enrichment of extracellular vesicles from plasma reveals mRNA changes associated with acute ischemic stroke Wijerathne, Harshani Witek, Malgorzata A. Jackson, Joshua M. Brown, Virginia Hupert, Mateusz L. Herrera, Kristina Kramer, Cameron Davidow, Abigail E. Li, Yan Baird, Alison E. Murphy, Michael C. Soper, Steven A. Commun Biol Article Currently there is no in vitro diagnostic test for acute ischemic stroke (AIS), yet rapid diagnosis is crucial for effective thrombolytic treatment. We previously demonstrated the utility of CD8(+) T-cells’ mRNA expression for AIS detection; however extracellular vesicles (EVs) were not evaluated as a source of mRNA for AIS testing. We now report a microfluidic device for the rapid and efficient affinity-enrichment of CD8(+) EVs and subsequent EV’s mRNA analysis using droplet digital PCR (ddPCR). The microfluidic device contains a dense array of micropillars modified with anti-CD8α monoclonal antibodies that enriched 158 ± 10 nm sized EVs at 4.3 ± 2.1 × 10(9) particles/100 µL of plasma. Analysis of mRNA from CD8(+) EVs and their parental T-cells revealed correlation in the expression for AIS-specific genes in both cell lines and healthy donors. In a blinded study, 80% test positivity for AIS patients and controls was revealed with a total analysis time of 3.7 h. Nature Publishing Group UK 2020-10-26 /pmc/articles/PMC7589468/ /pubmed/33106557 http://dx.doi.org/10.1038/s42003-020-01336-y 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 Wijerathne, Harshani Witek, Malgorzata A. Jackson, Joshua M. Brown, Virginia Hupert, Mateusz L. Herrera, Kristina Kramer, Cameron Davidow, Abigail E. Li, Yan Baird, Alison E. Murphy, Michael C. Soper, Steven A. Affinity enrichment of extracellular vesicles from plasma reveals mRNA changes associated with acute ischemic stroke |
title | Affinity enrichment of extracellular vesicles from plasma reveals mRNA changes associated with acute ischemic stroke |
title_full | Affinity enrichment of extracellular vesicles from plasma reveals mRNA changes associated with acute ischemic stroke |
title_fullStr | Affinity enrichment of extracellular vesicles from plasma reveals mRNA changes associated with acute ischemic stroke |
title_full_unstemmed | Affinity enrichment of extracellular vesicles from plasma reveals mRNA changes associated with acute ischemic stroke |
title_short | Affinity enrichment of extracellular vesicles from plasma reveals mRNA changes associated with acute ischemic stroke |
title_sort | affinity enrichment of extracellular vesicles from plasma reveals mrna changes associated with acute ischemic stroke |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589468/ https://www.ncbi.nlm.nih.gov/pubmed/33106557 http://dx.doi.org/10.1038/s42003-020-01336-y |
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