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Distinctive proteomic profiles among different regions of human carotid plaques in men and women

The heterogeneity of atherosclerotic tissue has limited comprehension in proteomic and metabolomic analyses. To elucidate the functional implications, and differences between genders, of atherosclerotic lesion formation we investigated protein profiles from different regions of human carotid atheros...

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Autores principales: Liang, Wenzhao, Ward, Liam J., Karlsson, Helen, Ljunggren, Stefan A., Li, Wei, Lindahl, Mats, Yuan, Xi-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873748/
https://www.ncbi.nlm.nih.gov/pubmed/27198765
http://dx.doi.org/10.1038/srep26231
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author Liang, Wenzhao
Ward, Liam J.
Karlsson, Helen
Ljunggren, Stefan A.
Li, Wei
Lindahl, Mats
Yuan, Xi-Ming
author_facet Liang, Wenzhao
Ward, Liam J.
Karlsson, Helen
Ljunggren, Stefan A.
Li, Wei
Lindahl, Mats
Yuan, Xi-Ming
author_sort Liang, Wenzhao
collection PubMed
description The heterogeneity of atherosclerotic tissue has limited comprehension in proteomic and metabolomic analyses. To elucidate the functional implications, and differences between genders, of atherosclerotic lesion formation we investigated protein profiles from different regions of human carotid atherosclerotic arteries; internal control, fatty streak, plaque shoulder, plaque centre, and fibrous cap. Proteomic analysis was performed using 2-DE with MALDI-TOF, with validation using nLC-MS/MS. Protein mapping of 2-DE identified 52 unique proteins, including 15 previously unmapped proteins, of which 41 proteins were confirmed by nLC-MS/MS analysis. Expression levels of 18 proteins were significantly altered in plaque regions compared to the internal control region. Nine proteins showed site-specific alterations, irrespective of gender, with clear associations to extracellular matrix remodelling. Five proteins display gender-specific alterations with 2-DE, with two alterations validated by nLC-MS/MS. Gender differences in ferritin light chain and transthyretin were validated using both techniques. Validation of immunohistochemistry confirmed significantly higher levels of ferritin in plaques from male patients. Proteomic analysis of different plaque regions has reduced the effects of plaque heterogeneity, and significant differences in protein expression are determined in specific regions and between genders. These proteomes have functional implications in plaque progression and are of importance in understanding gender differences in atherosclerosis.
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spelling pubmed-48737482016-06-02 Distinctive proteomic profiles among different regions of human carotid plaques in men and women Liang, Wenzhao Ward, Liam J. Karlsson, Helen Ljunggren, Stefan A. Li, Wei Lindahl, Mats Yuan, Xi-Ming Sci Rep Article The heterogeneity of atherosclerotic tissue has limited comprehension in proteomic and metabolomic analyses. To elucidate the functional implications, and differences between genders, of atherosclerotic lesion formation we investigated protein profiles from different regions of human carotid atherosclerotic arteries; internal control, fatty streak, plaque shoulder, plaque centre, and fibrous cap. Proteomic analysis was performed using 2-DE with MALDI-TOF, with validation using nLC-MS/MS. Protein mapping of 2-DE identified 52 unique proteins, including 15 previously unmapped proteins, of which 41 proteins were confirmed by nLC-MS/MS analysis. Expression levels of 18 proteins were significantly altered in plaque regions compared to the internal control region. Nine proteins showed site-specific alterations, irrespective of gender, with clear associations to extracellular matrix remodelling. Five proteins display gender-specific alterations with 2-DE, with two alterations validated by nLC-MS/MS. Gender differences in ferritin light chain and transthyretin were validated using both techniques. Validation of immunohistochemistry confirmed significantly higher levels of ferritin in plaques from male patients. Proteomic analysis of different plaque regions has reduced the effects of plaque heterogeneity, and significant differences in protein expression are determined in specific regions and between genders. These proteomes have functional implications in plaque progression and are of importance in understanding gender differences in atherosclerosis. Nature Publishing Group 2016-05-20 /pmc/articles/PMC4873748/ /pubmed/27198765 http://dx.doi.org/10.1038/srep26231 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Liang, Wenzhao
Ward, Liam J.
Karlsson, Helen
Ljunggren, Stefan A.
Li, Wei
Lindahl, Mats
Yuan, Xi-Ming
Distinctive proteomic profiles among different regions of human carotid plaques in men and women
title Distinctive proteomic profiles among different regions of human carotid plaques in men and women
title_full Distinctive proteomic profiles among different regions of human carotid plaques in men and women
title_fullStr Distinctive proteomic profiles among different regions of human carotid plaques in men and women
title_full_unstemmed Distinctive proteomic profiles among different regions of human carotid plaques in men and women
title_short Distinctive proteomic profiles among different regions of human carotid plaques in men and women
title_sort distinctive proteomic profiles among different regions of human carotid plaques in men and women
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873748/
https://www.ncbi.nlm.nih.gov/pubmed/27198765
http://dx.doi.org/10.1038/srep26231
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