Cargando…
Effect of different decellularization protocols on reendothelialization with human cells for a perfused renal bioscaffold of the rat
BACKGROUND: Scaffolds for tissue engineering can be received by whole organ decellularization while maintaining the site-specific extracellular matrix and the vascular tree. One among other decellularization techniques is the perfusion-based method using specific agents e.g. SDS for the elimination...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10022115/ https://www.ncbi.nlm.nih.gov/pubmed/36927344 http://dx.doi.org/10.1186/s12896-022-00767-1 |
_version_ | 1784908658234097664 |
---|---|
author | Sauter, Johannes Degenhardt, Hannes Tuebel, Jutta Foehr, Peter Knoeckel, Philipp Florian, Kira Charitou, Fiona Burgkart, Rainer Schmitt, Andreas |
author_facet | Sauter, Johannes Degenhardt, Hannes Tuebel, Jutta Foehr, Peter Knoeckel, Philipp Florian, Kira Charitou, Fiona Burgkart, Rainer Schmitt, Andreas |
author_sort | Sauter, Johannes |
collection | PubMed |
description | BACKGROUND: Scaffolds for tissue engineering can be received by whole organ decellularization while maintaining the site-specific extracellular matrix and the vascular tree. One among other decellularization techniques is the perfusion-based method using specific agents e.g. SDS for the elimination of cellular components. While SDS can disrupt the composition of the extracellular matrix and impair the adherence and growth of site-specific cells there are indications that xenogeneic cell types may benefit from protein denaturation by using higher detergent concentrations. The aim of this work is to investigate the effect of two different SDS-concentrations (i.e. 0.66% and 3%) on the ability of human endothelial cells to adhere and proliferate in an acellular rat kidney scaffold. MATERIAL AND METHODS: Acellular rat kidney scaffold was obtained by perfusion-based decellularization through the renal artery using a standardized protocol including SDS at concentrations of 0.66% or 3%. Subsequently cell seeding was performed with human immortalized endothelial cells EA.hy 926 via the renal artery. Recellularized kidneys were harvested after five days of pressure-controlled dynamic culture followed sectioning, histochemical and immunohistochemical staining as well as semiquantitative analysis. RESULTS: Efficacy of decellularization was verified by absence of cellular components as well as preservation of ultrastructure and adhesive proteins of the extracellular matrix. In semiquantitative analysis of recellularization, cell count after five days of dynamic culture more than doubled when using the gentle decellularization protocol with a concentration of SDS at 0.66% compared to 3%. Detectable cells maintained their endothelial phenotype and presented proliferative behavior while only a negligible fraction underwent apoptosis. CONCLUSION: Recellularization of acellular kidney scaffold with endothelial cells EA.hy 926 seeded through the renal artery benefits from gentle decellularization procedure. Because of that, decellularization with a SDS concentration at 0.66% should be preferred in further studies and coculture experiments. |
format | Online Article Text |
id | pubmed-10022115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100221152023-03-18 Effect of different decellularization protocols on reendothelialization with human cells for a perfused renal bioscaffold of the rat Sauter, Johannes Degenhardt, Hannes Tuebel, Jutta Foehr, Peter Knoeckel, Philipp Florian, Kira Charitou, Fiona Burgkart, Rainer Schmitt, Andreas BMC Biotechnol Research BACKGROUND: Scaffolds for tissue engineering can be received by whole organ decellularization while maintaining the site-specific extracellular matrix and the vascular tree. One among other decellularization techniques is the perfusion-based method using specific agents e.g. SDS for the elimination of cellular components. While SDS can disrupt the composition of the extracellular matrix and impair the adherence and growth of site-specific cells there are indications that xenogeneic cell types may benefit from protein denaturation by using higher detergent concentrations. The aim of this work is to investigate the effect of two different SDS-concentrations (i.e. 0.66% and 3%) on the ability of human endothelial cells to adhere and proliferate in an acellular rat kidney scaffold. MATERIAL AND METHODS: Acellular rat kidney scaffold was obtained by perfusion-based decellularization through the renal artery using a standardized protocol including SDS at concentrations of 0.66% or 3%. Subsequently cell seeding was performed with human immortalized endothelial cells EA.hy 926 via the renal artery. Recellularized kidneys were harvested after five days of pressure-controlled dynamic culture followed sectioning, histochemical and immunohistochemical staining as well as semiquantitative analysis. RESULTS: Efficacy of decellularization was verified by absence of cellular components as well as preservation of ultrastructure and adhesive proteins of the extracellular matrix. In semiquantitative analysis of recellularization, cell count after five days of dynamic culture more than doubled when using the gentle decellularization protocol with a concentration of SDS at 0.66% compared to 3%. Detectable cells maintained their endothelial phenotype and presented proliferative behavior while only a negligible fraction underwent apoptosis. CONCLUSION: Recellularization of acellular kidney scaffold with endothelial cells EA.hy 926 seeded through the renal artery benefits from gentle decellularization procedure. Because of that, decellularization with a SDS concentration at 0.66% should be preferred in further studies and coculture experiments. BioMed Central 2023-03-16 /pmc/articles/PMC10022115/ /pubmed/36927344 http://dx.doi.org/10.1186/s12896-022-00767-1 Text en © The Author(s) 2023 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 Sauter, Johannes Degenhardt, Hannes Tuebel, Jutta Foehr, Peter Knoeckel, Philipp Florian, Kira Charitou, Fiona Burgkart, Rainer Schmitt, Andreas Effect of different decellularization protocols on reendothelialization with human cells for a perfused renal bioscaffold of the rat |
title | Effect of different decellularization protocols on reendothelialization with human cells for a perfused renal bioscaffold of the rat |
title_full | Effect of different decellularization protocols on reendothelialization with human cells for a perfused renal bioscaffold of the rat |
title_fullStr | Effect of different decellularization protocols on reendothelialization with human cells for a perfused renal bioscaffold of the rat |
title_full_unstemmed | Effect of different decellularization protocols on reendothelialization with human cells for a perfused renal bioscaffold of the rat |
title_short | Effect of different decellularization protocols on reendothelialization with human cells for a perfused renal bioscaffold of the rat |
title_sort | effect of different decellularization protocols on reendothelialization with human cells for a perfused renal bioscaffold of the rat |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10022115/ https://www.ncbi.nlm.nih.gov/pubmed/36927344 http://dx.doi.org/10.1186/s12896-022-00767-1 |
work_keys_str_mv | AT sauterjohannes effectofdifferentdecellularizationprotocolsonreendothelializationwithhumancellsforaperfusedrenalbioscaffoldoftherat AT degenhardthannes effectofdifferentdecellularizationprotocolsonreendothelializationwithhumancellsforaperfusedrenalbioscaffoldoftherat AT tuebeljutta effectofdifferentdecellularizationprotocolsonreendothelializationwithhumancellsforaperfusedrenalbioscaffoldoftherat AT foehrpeter effectofdifferentdecellularizationprotocolsonreendothelializationwithhumancellsforaperfusedrenalbioscaffoldoftherat AT knoeckelphilipp effectofdifferentdecellularizationprotocolsonreendothelializationwithhumancellsforaperfusedrenalbioscaffoldoftherat AT floriankira effectofdifferentdecellularizationprotocolsonreendothelializationwithhumancellsforaperfusedrenalbioscaffoldoftherat AT charitoufiona effectofdifferentdecellularizationprotocolsonreendothelializationwithhumancellsforaperfusedrenalbioscaffoldoftherat AT burgkartrainer effectofdifferentdecellularizationprotocolsonreendothelializationwithhumancellsforaperfusedrenalbioscaffoldoftherat AT schmittandreas effectofdifferentdecellularizationprotocolsonreendothelializationwithhumancellsforaperfusedrenalbioscaffoldoftherat |