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Wnt5a, TLR2 and TLR4 are elevated in advanced human atherosclerotic lesions
OBJECTIVE AND DESIGN: Atherosclerosis (ATH) is a chronic inflammatory disease that involves cascades of signaling events mediated by various effector proteins. Here we sought to determine if the expression of Wnt5a, a secreted glycoprotein, is altered in discrete regions of the arterial plaque. METH...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Basel
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950563/ https://www.ncbi.nlm.nih.gov/pubmed/24346141 http://dx.doi.org/10.1007/s00011-013-0697-x |
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author | Malgor, Ramiro Bhatt, Pooja M. Connolly, Beth A. Jacoby, Denise L. Feldmann, Kyle J. Silver, Mitchell J. Nakazawa, Masato McCall, Kelly D. Goetz, Douglas J. |
author_facet | Malgor, Ramiro Bhatt, Pooja M. Connolly, Beth A. Jacoby, Denise L. Feldmann, Kyle J. Silver, Mitchell J. Nakazawa, Masato McCall, Kelly D. Goetz, Douglas J. |
author_sort | Malgor, Ramiro |
collection | PubMed |
description | OBJECTIVE AND DESIGN: Atherosclerosis (ATH) is a chronic inflammatory disease that involves cascades of signaling events mediated by various effector proteins. Here we sought to determine if the expression of Wnt5a, a secreted glycoprotein, is altered in discrete regions of the arterial plaque. METHODS: Atherosclerotic plaque tissues from 14 human subjects undergoing elective carotid endarterectomy were used in this study. Immunohistochemistry and laser capture microdissection combined with quantitative real-time PCR were used to determine the expression of Wnt5a and Toll-like receptors (TLRs) in different sections of the arterial lesions. Atherosclerotic serum samples (n = 30) and serum from healthy subjects (n = 16) were quantified for Wnt5a using an enzyme-linked immunosorbent assay (ELISA). RESULTS: The data analysis revealed that Wnt5a transcripts and protein were elevated in advanced arterial lesions relative to less advanced arterial lesions; that Wnt5a expression correlated with the presence of TLR4 and TLR2 transcripts; and that the average amount of Wnt5a protein present in atherosclerotic patient serum was significantly higher compared to healthy controls. CONCLUSIONS: This study is the first to provide evidence that the expression of Wnt5a increases as the disease progresses to a more advanced stage, and that this expression is coincident with that of TLR2 and TLR4. In addition, we found that the average Wnt5a levels in the serum of atherosclerotic patients are elevated relative to healthy controls, which is consistent with the hypothesis that Wnt5a plays a role in ATH. |
format | Online Article Text |
id | pubmed-3950563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Basel |
record_format | MEDLINE/PubMed |
spelling | pubmed-39505632014-03-20 Wnt5a, TLR2 and TLR4 are elevated in advanced human atherosclerotic lesions Malgor, Ramiro Bhatt, Pooja M. Connolly, Beth A. Jacoby, Denise L. Feldmann, Kyle J. Silver, Mitchell J. Nakazawa, Masato McCall, Kelly D. Goetz, Douglas J. Inflamm Res Original Research Paper OBJECTIVE AND DESIGN: Atherosclerosis (ATH) is a chronic inflammatory disease that involves cascades of signaling events mediated by various effector proteins. Here we sought to determine if the expression of Wnt5a, a secreted glycoprotein, is altered in discrete regions of the arterial plaque. METHODS: Atherosclerotic plaque tissues from 14 human subjects undergoing elective carotid endarterectomy were used in this study. Immunohistochemistry and laser capture microdissection combined with quantitative real-time PCR were used to determine the expression of Wnt5a and Toll-like receptors (TLRs) in different sections of the arterial lesions. Atherosclerotic serum samples (n = 30) and serum from healthy subjects (n = 16) were quantified for Wnt5a using an enzyme-linked immunosorbent assay (ELISA). RESULTS: The data analysis revealed that Wnt5a transcripts and protein were elevated in advanced arterial lesions relative to less advanced arterial lesions; that Wnt5a expression correlated with the presence of TLR4 and TLR2 transcripts; and that the average amount of Wnt5a protein present in atherosclerotic patient serum was significantly higher compared to healthy controls. CONCLUSIONS: This study is the first to provide evidence that the expression of Wnt5a increases as the disease progresses to a more advanced stage, and that this expression is coincident with that of TLR2 and TLR4. In addition, we found that the average Wnt5a levels in the serum of atherosclerotic patients are elevated relative to healthy controls, which is consistent with the hypothesis that Wnt5a plays a role in ATH. Springer Basel 2013-12-18 2014 /pmc/articles/PMC3950563/ /pubmed/24346141 http://dx.doi.org/10.1007/s00011-013-0697-x Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Research Paper Malgor, Ramiro Bhatt, Pooja M. Connolly, Beth A. Jacoby, Denise L. Feldmann, Kyle J. Silver, Mitchell J. Nakazawa, Masato McCall, Kelly D. Goetz, Douglas J. Wnt5a, TLR2 and TLR4 are elevated in advanced human atherosclerotic lesions |
title | Wnt5a, TLR2 and TLR4 are elevated in advanced human atherosclerotic lesions |
title_full | Wnt5a, TLR2 and TLR4 are elevated in advanced human atherosclerotic lesions |
title_fullStr | Wnt5a, TLR2 and TLR4 are elevated in advanced human atherosclerotic lesions |
title_full_unstemmed | Wnt5a, TLR2 and TLR4 are elevated in advanced human atherosclerotic lesions |
title_short | Wnt5a, TLR2 and TLR4 are elevated in advanced human atherosclerotic lesions |
title_sort | wnt5a, tlr2 and tlr4 are elevated in advanced human atherosclerotic lesions |
topic | Original Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950563/ https://www.ncbi.nlm.nih.gov/pubmed/24346141 http://dx.doi.org/10.1007/s00011-013-0697-x |
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