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Challenges of aortic valve tissue culture – maintenance of viability and extracellular matrix in the pulsatile dynamic microphysiological system

BACKGROUND: Calcific aortic valve disease (CAVD) causes an increasing health burden in the 21(st) century due to aging population. The complex pathophysiology remains to be understood to develop novel prevention and treatment strategies. Microphysiological systems (MPSs), also known as organ-on-chip...

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Autores principales: Dittfeld, Claudia, Winkelkotte, Maximilian, Scheer, Anna, Voigt, Emmely, Schmieder, Florian, Behrens, Stephan, Jannasch, Anett, Matschke, Klaus, Sonntag, Frank, Tugtekin, Sems-Malte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538250/
https://www.ncbi.nlm.nih.gov/pubmed/37770970
http://dx.doi.org/10.1186/s13036-023-00377-1
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author Dittfeld, Claudia
Winkelkotte, Maximilian
Scheer, Anna
Voigt, Emmely
Schmieder, Florian
Behrens, Stephan
Jannasch, Anett
Matschke, Klaus
Sonntag, Frank
Tugtekin, Sems-Malte
author_facet Dittfeld, Claudia
Winkelkotte, Maximilian
Scheer, Anna
Voigt, Emmely
Schmieder, Florian
Behrens, Stephan
Jannasch, Anett
Matschke, Klaus
Sonntag, Frank
Tugtekin, Sems-Malte
author_sort Dittfeld, Claudia
collection PubMed
description BACKGROUND: Calcific aortic valve disease (CAVD) causes an increasing health burden in the 21(st) century due to aging population. The complex pathophysiology remains to be understood to develop novel prevention and treatment strategies. Microphysiological systems (MPSs), also known as organ-on-chip or lab-on-a-chip systems, proved promising in bridging in vitro and in vivo approaches by applying integer AV tissue and modelling biomechanical microenvironment. This study introduces a novel MPS comprising different micropumps in conjunction with a tissue-incubation-chamber (TIC) for long-term porcine and human AV incubation (pAV, hAV). RESULTS: Tissue cultures in two different MPS setups were compared and validated by a bimodal viability analysis and extracellular matrix transformation assessment. The MPS-TIC conjunction proved applicable for incubation periods of 14–26 days. An increased metabolic rate was detected for pulsatile dynamic MPS culture compared to static condition indicated by increased LDH intensity. ECM changes such as an increase of collagen fibre content in line with tissue contraction and mass reduction, also observed in early CAVD, were detected in MPS-TIC culture, as well as an increase of collagen fibre content. Glycosaminoglycans remained stable, no significant alterations of α-SMA or CD31 epitopes and no accumulation of calciumhydroxyapatite were observed after 14 days of incubation. CONCLUSIONS: The presented ex vivo MPS allows long-term AV tissue incubation and will be adopted for future investigation of CAVD pathophysiology, also implementing human tissues. The bimodal viability assessment and ECM analyses approve reliability of ex vivo CAVD investigation and comparability of parallel tissue segments with different treatment strategies regarding the AV (patho)physiology. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13036-023-00377-1.
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spelling pubmed-105382502023-09-29 Challenges of aortic valve tissue culture – maintenance of viability and extracellular matrix in the pulsatile dynamic microphysiological system Dittfeld, Claudia Winkelkotte, Maximilian Scheer, Anna Voigt, Emmely Schmieder, Florian Behrens, Stephan Jannasch, Anett Matschke, Klaus Sonntag, Frank Tugtekin, Sems-Malte J Biol Eng Research BACKGROUND: Calcific aortic valve disease (CAVD) causes an increasing health burden in the 21(st) century due to aging population. The complex pathophysiology remains to be understood to develop novel prevention and treatment strategies. Microphysiological systems (MPSs), also known as organ-on-chip or lab-on-a-chip systems, proved promising in bridging in vitro and in vivo approaches by applying integer AV tissue and modelling biomechanical microenvironment. This study introduces a novel MPS comprising different micropumps in conjunction with a tissue-incubation-chamber (TIC) for long-term porcine and human AV incubation (pAV, hAV). RESULTS: Tissue cultures in two different MPS setups were compared and validated by a bimodal viability analysis and extracellular matrix transformation assessment. The MPS-TIC conjunction proved applicable for incubation periods of 14–26 days. An increased metabolic rate was detected for pulsatile dynamic MPS culture compared to static condition indicated by increased LDH intensity. ECM changes such as an increase of collagen fibre content in line with tissue contraction and mass reduction, also observed in early CAVD, were detected in MPS-TIC culture, as well as an increase of collagen fibre content. Glycosaminoglycans remained stable, no significant alterations of α-SMA or CD31 epitopes and no accumulation of calciumhydroxyapatite were observed after 14 days of incubation. CONCLUSIONS: The presented ex vivo MPS allows long-term AV tissue incubation and will be adopted for future investigation of CAVD pathophysiology, also implementing human tissues. The bimodal viability assessment and ECM analyses approve reliability of ex vivo CAVD investigation and comparability of parallel tissue segments with different treatment strategies regarding the AV (patho)physiology. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13036-023-00377-1. BioMed Central 2023-09-28 /pmc/articles/PMC10538250/ /pubmed/37770970 http://dx.doi.org/10.1186/s13036-023-00377-1 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 Research
Dittfeld, Claudia
Winkelkotte, Maximilian
Scheer, Anna
Voigt, Emmely
Schmieder, Florian
Behrens, Stephan
Jannasch, Anett
Matschke, Klaus
Sonntag, Frank
Tugtekin, Sems-Malte
Challenges of aortic valve tissue culture – maintenance of viability and extracellular matrix in the pulsatile dynamic microphysiological system
title Challenges of aortic valve tissue culture – maintenance of viability and extracellular matrix in the pulsatile dynamic microphysiological system
title_full Challenges of aortic valve tissue culture – maintenance of viability and extracellular matrix in the pulsatile dynamic microphysiological system
title_fullStr Challenges of aortic valve tissue culture – maintenance of viability and extracellular matrix in the pulsatile dynamic microphysiological system
title_full_unstemmed Challenges of aortic valve tissue culture – maintenance of viability and extracellular matrix in the pulsatile dynamic microphysiological system
title_short Challenges of aortic valve tissue culture – maintenance of viability and extracellular matrix in the pulsatile dynamic microphysiological system
title_sort challenges of aortic valve tissue culture – maintenance of viability and extracellular matrix in the pulsatile dynamic microphysiological system
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538250/
https://www.ncbi.nlm.nih.gov/pubmed/37770970
http://dx.doi.org/10.1186/s13036-023-00377-1
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