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Searching for new molecular markers for cells obtained from abdominal aortic aneurysm
The aim of the study was to investigate specific potential markers for cells obtained from three layers of human AAA divided into three segments along the AAA based on morphological differences. The isolated cells were compared to control commercial cell types from healthy human abdominal aortas. Fo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357660/ https://www.ncbi.nlm.nih.gov/pubmed/34080122 http://dx.doi.org/10.1007/s13353-021-00641-4 |
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author | Lesiak, Marta Augusciak-Duma, Aleksandra Stepien, Karolina L. Fus-Kujawa, Agnieszka Botor, Malwina Sieron, Aleksander L. |
author_facet | Lesiak, Marta Augusciak-Duma, Aleksandra Stepien, Karolina L. Fus-Kujawa, Agnieszka Botor, Malwina Sieron, Aleksander L. |
author_sort | Lesiak, Marta |
collection | PubMed |
description | The aim of the study was to investigate specific potential markers for cells obtained from three layers of human AAA divided into three segments along the AAA based on morphological differences. The isolated cells were compared to control commercial cell types from healthy human abdominal aortas. For each type of aortic layer, three specimens from 6 patients were compared. Total RNA was isolated from 36 cell cultures for gene expression profiling and potential new cytometry markers were typed. Isolated cells were analyzed by flow cytometry by using fluorochrome-conjugated antibodies to markers: CNN1, MYH10, ENG, ICAM2, and TEK. The relative expression of 45 genes in primary cell cultures and control lines was analyzed. Statistically significant differences were found in the expression of most of the analyzed genes between individual layers and control lines. Based on relative expression, antibodies were selected for flow cytometry. Gene expression profiles allowed to select new potential cytometry markers: CNN1, MYH10, MYOCD, ENG, ICAM2, TEK. However, none of the tested markers seems to be optimal and characteristic for a specific layer of AAA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13353-021-00641-4. |
format | Online Article Text |
id | pubmed-8357660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-83576602021-08-30 Searching for new molecular markers for cells obtained from abdominal aortic aneurysm Lesiak, Marta Augusciak-Duma, Aleksandra Stepien, Karolina L. Fus-Kujawa, Agnieszka Botor, Malwina Sieron, Aleksander L. J Appl Genet Human Genetics • Original Paper The aim of the study was to investigate specific potential markers for cells obtained from three layers of human AAA divided into three segments along the AAA based on morphological differences. The isolated cells were compared to control commercial cell types from healthy human abdominal aortas. For each type of aortic layer, three specimens from 6 patients were compared. Total RNA was isolated from 36 cell cultures for gene expression profiling and potential new cytometry markers were typed. Isolated cells were analyzed by flow cytometry by using fluorochrome-conjugated antibodies to markers: CNN1, MYH10, ENG, ICAM2, and TEK. The relative expression of 45 genes in primary cell cultures and control lines was analyzed. Statistically significant differences were found in the expression of most of the analyzed genes between individual layers and control lines. Based on relative expression, antibodies were selected for flow cytometry. Gene expression profiles allowed to select new potential cytometry markers: CNN1, MYH10, MYOCD, ENG, ICAM2, TEK. However, none of the tested markers seems to be optimal and characteristic for a specific layer of AAA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13353-021-00641-4. Springer Berlin Heidelberg 2021-06-02 2021 /pmc/articles/PMC8357660/ /pubmed/34080122 http://dx.doi.org/10.1007/s13353-021-00641-4 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/) . |
spellingShingle | Human Genetics • Original Paper Lesiak, Marta Augusciak-Duma, Aleksandra Stepien, Karolina L. Fus-Kujawa, Agnieszka Botor, Malwina Sieron, Aleksander L. Searching for new molecular markers for cells obtained from abdominal aortic aneurysm |
title | Searching for new molecular markers for cells obtained from abdominal aortic aneurysm |
title_full | Searching for new molecular markers for cells obtained from abdominal aortic aneurysm |
title_fullStr | Searching for new molecular markers for cells obtained from abdominal aortic aneurysm |
title_full_unstemmed | Searching for new molecular markers for cells obtained from abdominal aortic aneurysm |
title_short | Searching for new molecular markers for cells obtained from abdominal aortic aneurysm |
title_sort | searching for new molecular markers for cells obtained from abdominal aortic aneurysm |
topic | Human Genetics • Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357660/ https://www.ncbi.nlm.nih.gov/pubmed/34080122 http://dx.doi.org/10.1007/s13353-021-00641-4 |
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