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Distinct chemical composition and enzymatic treatment induced human endothelial cells survival in acellular ovine aortae
OBJECTIVE: The current experiment aimed to assess the impact of detergents such as 3% Triton X-100, 1% peracetic acid, 1% Tween-20, and 1% SDS in combination with Trypsin–EDTA on acellularization of ovine aortae after 7 days. RESULTS: Hematoxylin–Eosin staining showed an appropriate acellularization...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028817/ https://www.ncbi.nlm.nih.gov/pubmed/33827673 http://dx.doi.org/10.1186/s13104-021-05538-3 |
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author | Heidarzadeh, Morteza Rahbarghazi, Reza Saberianpour, Shirin Delkhosh, Aref Amini, Hassan Sokullu, Emel Hassanpour, Mehdi |
author_facet | Heidarzadeh, Morteza Rahbarghazi, Reza Saberianpour, Shirin Delkhosh, Aref Amini, Hassan Sokullu, Emel Hassanpour, Mehdi |
author_sort | Heidarzadeh, Morteza |
collection | PubMed |
description | OBJECTIVE: The current experiment aimed to assess the impact of detergents such as 3% Triton X-100, 1% peracetic acid, 1% Tween-20, and 1% SDS in combination with Trypsin–EDTA on acellularization of ovine aortae after 7 days. RESULTS: Hematoxylin–Eosin staining showed an appropriate acellularization rate in ovine aortae, indicated by a lack of cell nuclei in the tunica media layer. DAPI staining confirmed the lack of nuclei in the vascular wall after being exposed to the combination of chemical and enzymatic solutions. Verhoeff-Van Gieson staining showed that elastin fibers were diminished in acellular samples compared to the control group while collagen stands were unchanged. CCK-8 survival assay showed enhanced viability in human umbilical vein endothelial cells 5 days after being cultured on decellularized samples compared to the cells cultured on a plastic surface (p < 0.05). SEM imaging showed flattening of endothelial cells on the acellular surface. |
format | Online Article Text |
id | pubmed-8028817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80288172021-04-09 Distinct chemical composition and enzymatic treatment induced human endothelial cells survival in acellular ovine aortae Heidarzadeh, Morteza Rahbarghazi, Reza Saberianpour, Shirin Delkhosh, Aref Amini, Hassan Sokullu, Emel Hassanpour, Mehdi BMC Res Notes Research Note OBJECTIVE: The current experiment aimed to assess the impact of detergents such as 3% Triton X-100, 1% peracetic acid, 1% Tween-20, and 1% SDS in combination with Trypsin–EDTA on acellularization of ovine aortae after 7 days. RESULTS: Hematoxylin–Eosin staining showed an appropriate acellularization rate in ovine aortae, indicated by a lack of cell nuclei in the tunica media layer. DAPI staining confirmed the lack of nuclei in the vascular wall after being exposed to the combination of chemical and enzymatic solutions. Verhoeff-Van Gieson staining showed that elastin fibers were diminished in acellular samples compared to the control group while collagen stands were unchanged. CCK-8 survival assay showed enhanced viability in human umbilical vein endothelial cells 5 days after being cultured on decellularized samples compared to the cells cultured on a plastic surface (p < 0.05). SEM imaging showed flattening of endothelial cells on the acellular surface. BioMed Central 2021-04-07 /pmc/articles/PMC8028817/ /pubmed/33827673 http://dx.doi.org/10.1186/s13104-021-05538-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 | Research Note Heidarzadeh, Morteza Rahbarghazi, Reza Saberianpour, Shirin Delkhosh, Aref Amini, Hassan Sokullu, Emel Hassanpour, Mehdi Distinct chemical composition and enzymatic treatment induced human endothelial cells survival in acellular ovine aortae |
title | Distinct chemical composition and enzymatic treatment induced human endothelial cells survival in acellular ovine aortae |
title_full | Distinct chemical composition and enzymatic treatment induced human endothelial cells survival in acellular ovine aortae |
title_fullStr | Distinct chemical composition and enzymatic treatment induced human endothelial cells survival in acellular ovine aortae |
title_full_unstemmed | Distinct chemical composition and enzymatic treatment induced human endothelial cells survival in acellular ovine aortae |
title_short | Distinct chemical composition and enzymatic treatment induced human endothelial cells survival in acellular ovine aortae |
title_sort | distinct chemical composition and enzymatic treatment induced human endothelial cells survival in acellular ovine aortae |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028817/ https://www.ncbi.nlm.nih.gov/pubmed/33827673 http://dx.doi.org/10.1186/s13104-021-05538-3 |
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