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Neutrophils are important for the development of pro-reparative macrophages after irreversible electroporation of the liver in mice
Irreversible electroporation (IRE) is a non-thermal tissue ablative technology that has emerging applications in surgical oncology and regenerative surgery. To advance its therapeutic usefulness, it is important to understand the mechanisms through which IRE induces cell death and the role of the in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298444/ https://www.ncbi.nlm.nih.gov/pubmed/34294763 http://dx.doi.org/10.1038/s41598-021-94016-8 |
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author | Lopez-Ichikawa, Maya Vu, Ngan K. Nijagal, Amar Rubinsky, Boris Chang, Tammy T. |
author_facet | Lopez-Ichikawa, Maya Vu, Ngan K. Nijagal, Amar Rubinsky, Boris Chang, Tammy T. |
author_sort | Lopez-Ichikawa, Maya |
collection | PubMed |
description | Irreversible electroporation (IRE) is a non-thermal tissue ablative technology that has emerging applications in surgical oncology and regenerative surgery. To advance its therapeutic usefulness, it is important to understand the mechanisms through which IRE induces cell death and the role of the innate immune system in mediating subsequent regenerative repair. Through intravital imaging of the liver in mice, we show that IRE produces distinctive tissue injury features, including delayed yet robust recruitment of neutrophils, consistent with programmed necrosis. IRE treatment converts the monocyte/macrophage balance from pro-inflammatory to pro-reparative populations, and depletion of neutrophils inhibits this conversion. Reduced generation of pro-reparative Ly6C(lo)F4/80(hi) macrophages correlates with lower numbers of SOX9(+) hepatic progenitor cells in areas of macrophage clusters within the IRE injury zone. Our findings suggest that neutrophils play an important role in promoting the development of pro-reparative Ly6C(lo) monocytes/macrophages at the site of IRE injury, thus establishing conditions of regenerative repair. |
format | Online Article Text |
id | pubmed-8298444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82984442021-07-23 Neutrophils are important for the development of pro-reparative macrophages after irreversible electroporation of the liver in mice Lopez-Ichikawa, Maya Vu, Ngan K. Nijagal, Amar Rubinsky, Boris Chang, Tammy T. Sci Rep Article Irreversible electroporation (IRE) is a non-thermal tissue ablative technology that has emerging applications in surgical oncology and regenerative surgery. To advance its therapeutic usefulness, it is important to understand the mechanisms through which IRE induces cell death and the role of the innate immune system in mediating subsequent regenerative repair. Through intravital imaging of the liver in mice, we show that IRE produces distinctive tissue injury features, including delayed yet robust recruitment of neutrophils, consistent with programmed necrosis. IRE treatment converts the monocyte/macrophage balance from pro-inflammatory to pro-reparative populations, and depletion of neutrophils inhibits this conversion. Reduced generation of pro-reparative Ly6C(lo)F4/80(hi) macrophages correlates with lower numbers of SOX9(+) hepatic progenitor cells in areas of macrophage clusters within the IRE injury zone. Our findings suggest that neutrophils play an important role in promoting the development of pro-reparative Ly6C(lo) monocytes/macrophages at the site of IRE injury, thus establishing conditions of regenerative repair. Nature Publishing Group UK 2021-07-22 /pmc/articles/PMC8298444/ /pubmed/34294763 http://dx.doi.org/10.1038/s41598-021-94016-8 Text en © The Author(s) 2021 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/) . |
spellingShingle | Article Lopez-Ichikawa, Maya Vu, Ngan K. Nijagal, Amar Rubinsky, Boris Chang, Tammy T. Neutrophils are important for the development of pro-reparative macrophages after irreversible electroporation of the liver in mice |
title | Neutrophils are important for the development of pro-reparative macrophages after irreversible electroporation of the liver in mice |
title_full | Neutrophils are important for the development of pro-reparative macrophages after irreversible electroporation of the liver in mice |
title_fullStr | Neutrophils are important for the development of pro-reparative macrophages after irreversible electroporation of the liver in mice |
title_full_unstemmed | Neutrophils are important for the development of pro-reparative macrophages after irreversible electroporation of the liver in mice |
title_short | Neutrophils are important for the development of pro-reparative macrophages after irreversible electroporation of the liver in mice |
title_sort | neutrophils are important for the development of pro-reparative macrophages after irreversible electroporation of the liver in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298444/ https://www.ncbi.nlm.nih.gov/pubmed/34294763 http://dx.doi.org/10.1038/s41598-021-94016-8 |
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