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Extracellular matrix in ascending aortic aneurysms and dissections – What we learn from decellularization and scanning electron microscopy
Pathological impairment of elastic fiber and other extracellular matrix (ECM) components are described for the aortic media of ascending thoracic aortic aneurysms (aTAA) but the exact pathological impairment of the structure and its degree still needs further investigations. To evaluate the quantity...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422325/ https://www.ncbi.nlm.nih.gov/pubmed/30883576 http://dx.doi.org/10.1371/journal.pone.0213794 |
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author | Mimler, Teresa Nebert, Clemens Eichmair, Eva Winter, Birgitta Aschacher, Thomas Stelzmueller, Marie-Elisabeth Andreas, Martin Ehrlich, Marek Laufer, Guenther Messner, Barbara |
author_facet | Mimler, Teresa Nebert, Clemens Eichmair, Eva Winter, Birgitta Aschacher, Thomas Stelzmueller, Marie-Elisabeth Andreas, Martin Ehrlich, Marek Laufer, Guenther Messner, Barbara |
author_sort | Mimler, Teresa |
collection | PubMed |
description | Pathological impairment of elastic fiber and other extracellular matrix (ECM) components are described for the aortic media of ascending thoracic aortic aneurysms (aTAA) but the exact pathological impairment of the structure and its degree still needs further investigations. To evaluate the quantity and quality of elastic fiber sheets and other ECM structures (e.g. collagen), cells were removed from different types of aneurysmal tissues (tricuspid aortic valve [TAV] associated-, bicuspid aortic valve [BAV] associated-aneurysmal tissue and acute aortic dissections [AAD]) using 2.5% sodium hydroxide (NaOH) and compared to decellularized control aortic tissue. Likewise, native tissue has been analysed. To evaluate the 2D- (histological evaluation, fluorescence- and auto-fluorescence based staining methods) and the 3D structure (scanning electron microscopic [SEM] examination) of the medial layer we first analysed for a successful decellularization. After proving for successful decellularization, we quantified the amount of elastic fiber sheets, elastin and other ECM components including collagen. Aside from clearly visible focal elastic fiber loss in TAV-aTAA tissue, decellularization resulted in reduction of elastic fiber auto-fluorescence properties, which is perhaps an indication from a disease-related qualitative impairment of elastic fibers, visible only after contact with the alkaline solution. Likewise, the loss of collagen amount in BAV-aTAA and TAV-aTAA tissue (compared to non-decellularized tissue) after contact with NaOH indicates a prior disease-associated impairment of collagen. Although the amount of ECM was not changed in type A dissection tissue, detailed electron microscopic evaluation revealed changes in ECM quality, which worsened after contact with alkaline solution but were not visible after histological analyses. Apart from the improved observation of the samples using electron microscopy, contact of aneurysmal and dissected tissue with the alkaline decellularization solution revealed potential disease related changes in ECM quality which can partly be connected to already published data, but have to be proven by further studies. |
format | Online Article Text |
id | pubmed-6422325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64223252019-04-02 Extracellular matrix in ascending aortic aneurysms and dissections – What we learn from decellularization and scanning electron microscopy Mimler, Teresa Nebert, Clemens Eichmair, Eva Winter, Birgitta Aschacher, Thomas Stelzmueller, Marie-Elisabeth Andreas, Martin Ehrlich, Marek Laufer, Guenther Messner, Barbara PLoS One Research Article Pathological impairment of elastic fiber and other extracellular matrix (ECM) components are described for the aortic media of ascending thoracic aortic aneurysms (aTAA) but the exact pathological impairment of the structure and its degree still needs further investigations. To evaluate the quantity and quality of elastic fiber sheets and other ECM structures (e.g. collagen), cells were removed from different types of aneurysmal tissues (tricuspid aortic valve [TAV] associated-, bicuspid aortic valve [BAV] associated-aneurysmal tissue and acute aortic dissections [AAD]) using 2.5% sodium hydroxide (NaOH) and compared to decellularized control aortic tissue. Likewise, native tissue has been analysed. To evaluate the 2D- (histological evaluation, fluorescence- and auto-fluorescence based staining methods) and the 3D structure (scanning electron microscopic [SEM] examination) of the medial layer we first analysed for a successful decellularization. After proving for successful decellularization, we quantified the amount of elastic fiber sheets, elastin and other ECM components including collagen. Aside from clearly visible focal elastic fiber loss in TAV-aTAA tissue, decellularization resulted in reduction of elastic fiber auto-fluorescence properties, which is perhaps an indication from a disease-related qualitative impairment of elastic fibers, visible only after contact with the alkaline solution. Likewise, the loss of collagen amount in BAV-aTAA and TAV-aTAA tissue (compared to non-decellularized tissue) after contact with NaOH indicates a prior disease-associated impairment of collagen. Although the amount of ECM was not changed in type A dissection tissue, detailed electron microscopic evaluation revealed changes in ECM quality, which worsened after contact with alkaline solution but were not visible after histological analyses. Apart from the improved observation of the samples using electron microscopy, contact of aneurysmal and dissected tissue with the alkaline decellularization solution revealed potential disease related changes in ECM quality which can partly be connected to already published data, but have to be proven by further studies. Public Library of Science 2019-03-18 /pmc/articles/PMC6422325/ /pubmed/30883576 http://dx.doi.org/10.1371/journal.pone.0213794 Text en © 2019 Mimler et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Mimler, Teresa Nebert, Clemens Eichmair, Eva Winter, Birgitta Aschacher, Thomas Stelzmueller, Marie-Elisabeth Andreas, Martin Ehrlich, Marek Laufer, Guenther Messner, Barbara Extracellular matrix in ascending aortic aneurysms and dissections – What we learn from decellularization and scanning electron microscopy |
title | Extracellular matrix in ascending aortic aneurysms and dissections – What we learn from decellularization and scanning electron microscopy |
title_full | Extracellular matrix in ascending aortic aneurysms and dissections – What we learn from decellularization and scanning electron microscopy |
title_fullStr | Extracellular matrix in ascending aortic aneurysms and dissections – What we learn from decellularization and scanning electron microscopy |
title_full_unstemmed | Extracellular matrix in ascending aortic aneurysms and dissections – What we learn from decellularization and scanning electron microscopy |
title_short | Extracellular matrix in ascending aortic aneurysms and dissections – What we learn from decellularization and scanning electron microscopy |
title_sort | extracellular matrix in ascending aortic aneurysms and dissections – what we learn from decellularization and scanning electron microscopy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422325/ https://www.ncbi.nlm.nih.gov/pubmed/30883576 http://dx.doi.org/10.1371/journal.pone.0213794 |
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