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Comparative lipid profiling of murine and human atherosclerotic plaques using high-resolution MALDI MSI
The distribution of atherosclerotic lesions in the aorta and its branches of ApoE knockout (ApoE(−/−)) mice is like that of patients with atherosclerosis. By using high-resolution MALDI mass spectrometry imaging (MSI), we aimed at characterizing universally applicable physiological biomarkers by com...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766400/ https://www.ncbi.nlm.nih.gov/pubmed/34797426 http://dx.doi.org/10.1007/s00424-021-02643-x |
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author | Khamehgir-Silz, Pegah Gerbig, Stefanie Volk, Nadine Schulz, Sabine Spengler, Bernhard Hecker, Markus Wagner, Andreas H. |
author_facet | Khamehgir-Silz, Pegah Gerbig, Stefanie Volk, Nadine Schulz, Sabine Spengler, Bernhard Hecker, Markus Wagner, Andreas H. |
author_sort | Khamehgir-Silz, Pegah |
collection | PubMed |
description | The distribution of atherosclerotic lesions in the aorta and its branches of ApoE knockout (ApoE(−/−)) mice is like that of patients with atherosclerosis. By using high-resolution MALDI mass spectrometry imaging (MSI), we aimed at characterizing universally applicable physiological biomarkers by comparing the murine lipid marker profile with that of human atherosclerotic arteries. Therefore, the aorta or carotid artery of male ApoE(−/−) mice at different ages, human arteries with documented atherosclerotic changes originated from amputated limbs, and corresponding controls were analysed. Obtained data were subjected to multivariate statistical analysis to identify potential biomarkers. Thirty-one m/z values corresponding to individual lipid species of cholesterol esters, lysophosphatidylcholines, lysophosphatidylethanolamines, and cholesterol derivatives were found to be specific in aortic atherosclerotic plaques of old ApoE(−/−) mice. The lipid composition at related vessel positions of young ApoE(−/−) mice was more comparable with wild-type mice. Twenty-six m/z values of the murine lipid markers were found in human atherosclerotic peripheral arteries but also control vessels and showed a more patient-dependent diverse distribution. Extensive data analysis without marker preselection based on mouse data revealed lysophosphatidylcholine and glucosylated cholesterol species, the latter not being detected in the murine atherosclerotic tissue, as specific potential novel human atherosclerotic vessel markers. Despite the heterogeneous lipid profile of atherosclerotic peripheral arteries derived from human patients, we identified lipids specifically colocalized to atherosclerotic human tissue and plaques in ApoE(−/−) mice. These data highlight species-dependent differences in lipid profiles between peripheral artery disease and aortic atherosclerosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00424-021-02643-x. |
format | Online Article Text |
id | pubmed-8766400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-87664002022-02-02 Comparative lipid profiling of murine and human atherosclerotic plaques using high-resolution MALDI MSI Khamehgir-Silz, Pegah Gerbig, Stefanie Volk, Nadine Schulz, Sabine Spengler, Bernhard Hecker, Markus Wagner, Andreas H. Pflugers Arch Molecular and Cellular Mechanisms of Disease The distribution of atherosclerotic lesions in the aorta and its branches of ApoE knockout (ApoE(−/−)) mice is like that of patients with atherosclerosis. By using high-resolution MALDI mass spectrometry imaging (MSI), we aimed at characterizing universally applicable physiological biomarkers by comparing the murine lipid marker profile with that of human atherosclerotic arteries. Therefore, the aorta or carotid artery of male ApoE(−/−) mice at different ages, human arteries with documented atherosclerotic changes originated from amputated limbs, and corresponding controls were analysed. Obtained data were subjected to multivariate statistical analysis to identify potential biomarkers. Thirty-one m/z values corresponding to individual lipid species of cholesterol esters, lysophosphatidylcholines, lysophosphatidylethanolamines, and cholesterol derivatives were found to be specific in aortic atherosclerotic plaques of old ApoE(−/−) mice. The lipid composition at related vessel positions of young ApoE(−/−) mice was more comparable with wild-type mice. Twenty-six m/z values of the murine lipid markers were found in human atherosclerotic peripheral arteries but also control vessels and showed a more patient-dependent diverse distribution. Extensive data analysis without marker preselection based on mouse data revealed lysophosphatidylcholine and glucosylated cholesterol species, the latter not being detected in the murine atherosclerotic tissue, as specific potential novel human atherosclerotic vessel markers. Despite the heterogeneous lipid profile of atherosclerotic peripheral arteries derived from human patients, we identified lipids specifically colocalized to atherosclerotic human tissue and plaques in ApoE(−/−) mice. These data highlight species-dependent differences in lipid profiles between peripheral artery disease and aortic atherosclerosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00424-021-02643-x. Springer Berlin Heidelberg 2021-11-19 2022 /pmc/articles/PMC8766400/ /pubmed/34797426 http://dx.doi.org/10.1007/s00424-021-02643-x 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 | Molecular and Cellular Mechanisms of Disease Khamehgir-Silz, Pegah Gerbig, Stefanie Volk, Nadine Schulz, Sabine Spengler, Bernhard Hecker, Markus Wagner, Andreas H. Comparative lipid profiling of murine and human atherosclerotic plaques using high-resolution MALDI MSI |
title | Comparative lipid profiling of murine and human atherosclerotic plaques using high-resolution MALDI MSI |
title_full | Comparative lipid profiling of murine and human atherosclerotic plaques using high-resolution MALDI MSI |
title_fullStr | Comparative lipid profiling of murine and human atherosclerotic plaques using high-resolution MALDI MSI |
title_full_unstemmed | Comparative lipid profiling of murine and human atherosclerotic plaques using high-resolution MALDI MSI |
title_short | Comparative lipid profiling of murine and human atherosclerotic plaques using high-resolution MALDI MSI |
title_sort | comparative lipid profiling of murine and human atherosclerotic plaques using high-resolution maldi msi |
topic | Molecular and Cellular Mechanisms of Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766400/ https://www.ncbi.nlm.nih.gov/pubmed/34797426 http://dx.doi.org/10.1007/s00424-021-02643-x |
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