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Hydrostatic pressure can induce apoptosis of the skin

We previously showed that high hydrostatic pressure (HHP) treatment at 200 MPa for 10 min induced complete cell death in skin and skin tumors via necrosis. We used this technique to treat a giant congenital melanocytic nevus and reused the inactivated nevus tissue as a dermis autograft. However, ski...

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Autores principales: Le, Tien Minh, Morimoto, Naoki, Ly, Nhung Thi My, Mitsui, Toshihito, Notodihardjo, Sharon Claudia, Munisso, Maria Chiara, Kakudo, Natsuko, Moriyama, Hiroyuki, Yamaoka, Tetsuji, Kusumoto, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7572420/
https://www.ncbi.nlm.nih.gov/pubmed/33077833
http://dx.doi.org/10.1038/s41598-020-74695-5
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author Le, Tien Minh
Morimoto, Naoki
Ly, Nhung Thi My
Mitsui, Toshihito
Notodihardjo, Sharon Claudia
Munisso, Maria Chiara
Kakudo, Natsuko
Moriyama, Hiroyuki
Yamaoka, Tetsuji
Kusumoto, Kenji
author_facet Le, Tien Minh
Morimoto, Naoki
Ly, Nhung Thi My
Mitsui, Toshihito
Notodihardjo, Sharon Claudia
Munisso, Maria Chiara
Kakudo, Natsuko
Moriyama, Hiroyuki
Yamaoka, Tetsuji
Kusumoto, Kenji
author_sort Le, Tien Minh
collection PubMed
description We previously showed that high hydrostatic pressure (HHP) treatment at 200 MPa for 10 min induced complete cell death in skin and skin tumors via necrosis. We used this technique to treat a giant congenital melanocytic nevus and reused the inactivated nevus tissue as a dermis autograft. However, skin inactivated by HHP promoted inflammation in a preclinical study using a porcine model. Therefore, in the present study, we explored the pressurization conditions that induce apoptosis of the skin, as apoptotic cells are not believed to promote inflammation, so the engraftment of inactivated skin should be improved. Using a human dermal fibroblast cell line in suspension culture, we found that HHP at 50 MPa for ≥ 36 h completely induced fibroblast cell death via apoptosis based on the morphological changes in transmission electron microscopy, reactive oxygen species elevation, caspase activation and phosphatidylserine membrane translocation. Furthermore, immunohistochemistry with terminal deoxynucleotidyl transferase dUTP nick-end labeling and cleaved caspase-3 showed most cells in the skin inactivated by pressurization to be apoptotic. Consequently, in vivo grafting of apoptosis-induced inactivated skin resulted in successful engraftment and greater dermal cellular density and macrophage infiltration than our existing method. Our finding supports an alternative approach to hydrostatic pressure application.
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spelling pubmed-75724202020-10-21 Hydrostatic pressure can induce apoptosis of the skin Le, Tien Minh Morimoto, Naoki Ly, Nhung Thi My Mitsui, Toshihito Notodihardjo, Sharon Claudia Munisso, Maria Chiara Kakudo, Natsuko Moriyama, Hiroyuki Yamaoka, Tetsuji Kusumoto, Kenji Sci Rep Article We previously showed that high hydrostatic pressure (HHP) treatment at 200 MPa for 10 min induced complete cell death in skin and skin tumors via necrosis. We used this technique to treat a giant congenital melanocytic nevus and reused the inactivated nevus tissue as a dermis autograft. However, skin inactivated by HHP promoted inflammation in a preclinical study using a porcine model. Therefore, in the present study, we explored the pressurization conditions that induce apoptosis of the skin, as apoptotic cells are not believed to promote inflammation, so the engraftment of inactivated skin should be improved. Using a human dermal fibroblast cell line in suspension culture, we found that HHP at 50 MPa for ≥ 36 h completely induced fibroblast cell death via apoptosis based on the morphological changes in transmission electron microscopy, reactive oxygen species elevation, caspase activation and phosphatidylserine membrane translocation. Furthermore, immunohistochemistry with terminal deoxynucleotidyl transferase dUTP nick-end labeling and cleaved caspase-3 showed most cells in the skin inactivated by pressurization to be apoptotic. Consequently, in vivo grafting of apoptosis-induced inactivated skin resulted in successful engraftment and greater dermal cellular density and macrophage infiltration than our existing method. Our finding supports an alternative approach to hydrostatic pressure application. Nature Publishing Group UK 2020-10-19 /pmc/articles/PMC7572420/ /pubmed/33077833 http://dx.doi.org/10.1038/s41598-020-74695-5 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 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/.
spellingShingle Article
Le, Tien Minh
Morimoto, Naoki
Ly, Nhung Thi My
Mitsui, Toshihito
Notodihardjo, Sharon Claudia
Munisso, Maria Chiara
Kakudo, Natsuko
Moriyama, Hiroyuki
Yamaoka, Tetsuji
Kusumoto, Kenji
Hydrostatic pressure can induce apoptosis of the skin
title Hydrostatic pressure can induce apoptosis of the skin
title_full Hydrostatic pressure can induce apoptosis of the skin
title_fullStr Hydrostatic pressure can induce apoptosis of the skin
title_full_unstemmed Hydrostatic pressure can induce apoptosis of the skin
title_short Hydrostatic pressure can induce apoptosis of the skin
title_sort hydrostatic pressure can induce apoptosis of the skin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7572420/
https://www.ncbi.nlm.nih.gov/pubmed/33077833
http://dx.doi.org/10.1038/s41598-020-74695-5
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