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Nanobody-based pannexin1 channel inhibitors reduce inflammation in acute liver injury

BACKGROUND: The opening of pannexin1 channels is considered as a key event in inflammation. Pannexin1 channel-mediated release of adenosine triphosphate triggers inflammasome signaling and activation of immune cells. By doing so, pannexin1 channels play an important role in several inflammatory dise...

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Autores principales: Van Campenhout, Raf, De Groof, Timo W. M., Kadam, Prashant, Kwak, Brenda R., Muyldermans, Serge, Devoogdt, Nick, Vinken, Mathieu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10566086/
https://www.ncbi.nlm.nih.gov/pubmed/37821897
http://dx.doi.org/10.1186/s12951-023-02137-1
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author Van Campenhout, Raf
De Groof, Timo W. M.
Kadam, Prashant
Kwak, Brenda R.
Muyldermans, Serge
Devoogdt, Nick
Vinken, Mathieu
author_facet Van Campenhout, Raf
De Groof, Timo W. M.
Kadam, Prashant
Kwak, Brenda R.
Muyldermans, Serge
Devoogdt, Nick
Vinken, Mathieu
author_sort Van Campenhout, Raf
collection PubMed
description BACKGROUND: The opening of pannexin1 channels is considered as a key event in inflammation. Pannexin1 channel-mediated release of adenosine triphosphate triggers inflammasome signaling and activation of immune cells. By doing so, pannexin1 channels play an important role in several inflammatory diseases. Although pannexin1 channel inhibition could represent a novel clinical strategy for treatment of inflammatory disorders, therapeutic pannexin1 channel targeting is impeded by the lack of specific, potent and/or in vivo-applicable inhibitors. The goal of this study is to generate nanobody-based inhibitors of pannexin1 channels. RESULTS: Pannexin1-targeting nanobodies were developed as potential new pannexin1 channel inhibitors. We identified 3 cross-reactive nanobodies that showed affinity for both murine and human pannexin1 proteins. Flow cytometry experiments revealed binding capacities in the nanomolar range. Moreover, the pannexin1-targeting nanobodies were found to block pannexin1 channel-mediated release of adenosine triphosphate. The pannexin1-targeting nanobodies were also demonstrated to display anti-inflammatory effects in vitro through reduction of interleukin 1 beta amounts. This anti-inflammatory outcome was reproduced in vivo using a human-relevant mouse model of acute liver disease relying on acetaminophen overdosing. More specifically, the pannexin1-targeting nanobodies lowered serum levels of inflammatory cytokines and diminished liver damage. These effects were linked with alteration of the expression of several NLRP3 inflammasome components. CONCLUSIONS: This study introduced for the first time specific, potent and in vivo-applicable nanobody-based inhibitors of pannexin1 channels. As demonstrated for the case of liver disease, the pannexin1-targeting nanobodies hold great promise as anti-inflammatory agents, yet this should be further tested for extrahepatic inflammatory disorders. Moreover, the pannexin1-targeting nanobodies represent novel tools for fundamental research regarding the role of pannexin1 channels in pathological and physiological processes. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-02137-1.
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spelling pubmed-105660862023-10-12 Nanobody-based pannexin1 channel inhibitors reduce inflammation in acute liver injury Van Campenhout, Raf De Groof, Timo W. M. Kadam, Prashant Kwak, Brenda R. Muyldermans, Serge Devoogdt, Nick Vinken, Mathieu J Nanobiotechnology Methodology BACKGROUND: The opening of pannexin1 channels is considered as a key event in inflammation. Pannexin1 channel-mediated release of adenosine triphosphate triggers inflammasome signaling and activation of immune cells. By doing so, pannexin1 channels play an important role in several inflammatory diseases. Although pannexin1 channel inhibition could represent a novel clinical strategy for treatment of inflammatory disorders, therapeutic pannexin1 channel targeting is impeded by the lack of specific, potent and/or in vivo-applicable inhibitors. The goal of this study is to generate nanobody-based inhibitors of pannexin1 channels. RESULTS: Pannexin1-targeting nanobodies were developed as potential new pannexin1 channel inhibitors. We identified 3 cross-reactive nanobodies that showed affinity for both murine and human pannexin1 proteins. Flow cytometry experiments revealed binding capacities in the nanomolar range. Moreover, the pannexin1-targeting nanobodies were found to block pannexin1 channel-mediated release of adenosine triphosphate. The pannexin1-targeting nanobodies were also demonstrated to display anti-inflammatory effects in vitro through reduction of interleukin 1 beta amounts. This anti-inflammatory outcome was reproduced in vivo using a human-relevant mouse model of acute liver disease relying on acetaminophen overdosing. More specifically, the pannexin1-targeting nanobodies lowered serum levels of inflammatory cytokines and diminished liver damage. These effects were linked with alteration of the expression of several NLRP3 inflammasome components. CONCLUSIONS: This study introduced for the first time specific, potent and in vivo-applicable nanobody-based inhibitors of pannexin1 channels. As demonstrated for the case of liver disease, the pannexin1-targeting nanobodies hold great promise as anti-inflammatory agents, yet this should be further tested for extrahepatic inflammatory disorders. Moreover, the pannexin1-targeting nanobodies represent novel tools for fundamental research regarding the role of pannexin1 channels in pathological and physiological processes. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-02137-1. BioMed Central 2023-10-11 /pmc/articles/PMC10566086/ /pubmed/37821897 http://dx.doi.org/10.1186/s12951-023-02137-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology
Van Campenhout, Raf
De Groof, Timo W. M.
Kadam, Prashant
Kwak, Brenda R.
Muyldermans, Serge
Devoogdt, Nick
Vinken, Mathieu
Nanobody-based pannexin1 channel inhibitors reduce inflammation in acute liver injury
title Nanobody-based pannexin1 channel inhibitors reduce inflammation in acute liver injury
title_full Nanobody-based pannexin1 channel inhibitors reduce inflammation in acute liver injury
title_fullStr Nanobody-based pannexin1 channel inhibitors reduce inflammation in acute liver injury
title_full_unstemmed Nanobody-based pannexin1 channel inhibitors reduce inflammation in acute liver injury
title_short Nanobody-based pannexin1 channel inhibitors reduce inflammation in acute liver injury
title_sort nanobody-based pannexin1 channel inhibitors reduce inflammation in acute liver injury
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10566086/
https://www.ncbi.nlm.nih.gov/pubmed/37821897
http://dx.doi.org/10.1186/s12951-023-02137-1
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