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Ultra-fast and automated immunohistofluorescent multistaining using a microfluidic tissue processor

Multistaining of a tissue section targeting multiple markers allows to reveal complex interplays in a tumor environment. However, the resource-intensive and impractically long nature of iterative multiplexed immunostainings prohibits its practical implementation in daily routine, even when using wor...

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Autores principales: Cappi, Giulia, Dupouy, Diego Gabriel, Comino, Marta Aurelia, Ciftlik, Ata Tuna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418167/
https://www.ncbi.nlm.nih.gov/pubmed/30872751
http://dx.doi.org/10.1038/s41598-019-41119-y
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author Cappi, Giulia
Dupouy, Diego Gabriel
Comino, Marta Aurelia
Ciftlik, Ata Tuna
author_facet Cappi, Giulia
Dupouy, Diego Gabriel
Comino, Marta Aurelia
Ciftlik, Ata Tuna
author_sort Cappi, Giulia
collection PubMed
description Multistaining of a tissue section targeting multiple markers allows to reveal complex interplays in a tumor environment. However, the resource-intensive and impractically long nature of iterative multiplexed immunostainings prohibits its practical implementation in daily routine, even when using work-flow automation systems. Here, we report a fully automated and ultra-fast multistaining using a microfluidic tissue processor (MTP) in as short as 20 minutes per marker, by immunofluorescent staining employing commercially available tyramide signal amplification polymer precipitation by horse-radish peroxidase (HRP) activation. The reported duration includes (i) 15 minutes for the entire fluidic exchange and reagent incubation necessary for the immunostaining and (ii) 5 minutes for the heat-induced removal of the applied antibodies. Using the automated MTP, we demonstrated a 4-plex automated multistaining with clinically relevant biomarkers within 84 minutes, showing perfect agreement with the state-of-the-art microwave treatment antibody removal. The presented HRP-based method is in principle extendable to multistaining by both tyramides accommodating higher number of fluorescent channels and multi-color chromogenic staining. We anticipate that our automated multi-staining with a turn-around time shorter than existing monoplex immunohistochemistry methods has the potential to enable multistaining in routine without disturbing the current laboratory workflow, opening perspectives for implementation of -omics approaches in tissue diagnostics.
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spelling pubmed-64181672019-03-18 Ultra-fast and automated immunohistofluorescent multistaining using a microfluidic tissue processor Cappi, Giulia Dupouy, Diego Gabriel Comino, Marta Aurelia Ciftlik, Ata Tuna Sci Rep Article Multistaining of a tissue section targeting multiple markers allows to reveal complex interplays in a tumor environment. However, the resource-intensive and impractically long nature of iterative multiplexed immunostainings prohibits its practical implementation in daily routine, even when using work-flow automation systems. Here, we report a fully automated and ultra-fast multistaining using a microfluidic tissue processor (MTP) in as short as 20 minutes per marker, by immunofluorescent staining employing commercially available tyramide signal amplification polymer precipitation by horse-radish peroxidase (HRP) activation. The reported duration includes (i) 15 minutes for the entire fluidic exchange and reagent incubation necessary for the immunostaining and (ii) 5 minutes for the heat-induced removal of the applied antibodies. Using the automated MTP, we demonstrated a 4-plex automated multistaining with clinically relevant biomarkers within 84 minutes, showing perfect agreement with the state-of-the-art microwave treatment antibody removal. The presented HRP-based method is in principle extendable to multistaining by both tyramides accommodating higher number of fluorescent channels and multi-color chromogenic staining. We anticipate that our automated multi-staining with a turn-around time shorter than existing monoplex immunohistochemistry methods has the potential to enable multistaining in routine without disturbing the current laboratory workflow, opening perspectives for implementation of -omics approaches in tissue diagnostics. Nature Publishing Group UK 2019-03-14 /pmc/articles/PMC6418167/ /pubmed/30872751 http://dx.doi.org/10.1038/s41598-019-41119-y Text en © The Author(s) 2019 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
Cappi, Giulia
Dupouy, Diego Gabriel
Comino, Marta Aurelia
Ciftlik, Ata Tuna
Ultra-fast and automated immunohistofluorescent multistaining using a microfluidic tissue processor
title Ultra-fast and automated immunohistofluorescent multistaining using a microfluidic tissue processor
title_full Ultra-fast and automated immunohistofluorescent multistaining using a microfluidic tissue processor
title_fullStr Ultra-fast and automated immunohistofluorescent multistaining using a microfluidic tissue processor
title_full_unstemmed Ultra-fast and automated immunohistofluorescent multistaining using a microfluidic tissue processor
title_short Ultra-fast and automated immunohistofluorescent multistaining using a microfluidic tissue processor
title_sort ultra-fast and automated immunohistofluorescent multistaining using a microfluidic tissue processor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418167/
https://www.ncbi.nlm.nih.gov/pubmed/30872751
http://dx.doi.org/10.1038/s41598-019-41119-y
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