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Serum Amyloid A Facilitates Early Lesion Development in Ldlr(−/−) Mice

BACKGROUND: Atherosclerosis is a chronic inflammatory disorder, and several studies have demonstrated a positive association between plasma serum amyloid A (SAA) levels and cardiovascular disease risk. The aim of the study was to examine whether SAA has a role in atherogenesis, the underlying basis...

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Autores principales: Krishack, Paulette A, Bhanvadia, Clarissa V, Lukens, John, Sontag, Timothy J, De Beer, Maria C, Getz, Godfrey S, Reardon, Catherine A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608070/
https://www.ncbi.nlm.nih.gov/pubmed/26187995
http://dx.doi.org/10.1161/JAHA.115.001858
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author Krishack, Paulette A
Bhanvadia, Clarissa V
Lukens, John
Sontag, Timothy J
De Beer, Maria C
Getz, Godfrey S
Reardon, Catherine A
author_facet Krishack, Paulette A
Bhanvadia, Clarissa V
Lukens, John
Sontag, Timothy J
De Beer, Maria C
Getz, Godfrey S
Reardon, Catherine A
author_sort Krishack, Paulette A
collection PubMed
description BACKGROUND: Atherosclerosis is a chronic inflammatory disorder, and several studies have demonstrated a positive association between plasma serum amyloid A (SAA) levels and cardiovascular disease risk. The aim of the study was to examine whether SAA has a role in atherogenesis, the underlying basis of most cardiovascular disease. METHODS AND RESULTS: Mice globally deficient in acute-phase isoforms Saa1 and Saa2 (Saa(−/−)) were crossed to Ldlr(−/−) mice (Saa(−/−)Ldlr(−/−)). Saa(−/−)Ldlr(−/−) mice demonstrated a 31% reduction in lesional area in the ascending aorta but not in the aortic root or innominate artery after consuming a high-fat, high-cholesterol Western-type diet for 6 weeks. The lesions were predominantly macrophage foam cells. The phenotype was lost in more mature lesions in mice fed a Western-type diet for 12 weeks, suggesting that SAA is involved in early lesion development. The decreased atherosclerosis in the Saa(−/−)Ldlr(−/−) mice occurred despite increased levels of blood monocytes and was independent of plasma lipid levels. SAA is produced predominantly by hepatocytes and macrophages. To determine which source of SAA may have a dominant role in lesion development, bone marrow transplantation was performed. Ldlr(−/−) mice that received bone marrow from Saa(−/−)Ldlr(−/−) mice had slightly reduced ascending aorta atherosclerosis compared with Saa(−/−)Ldlr(−/−) mice receiving bone marrow from Ldlr(−/−) mice, indicating that the expression of SAA by macrophages may have an important influence on atherogenesis. CONCLUSIONS: The results indicate that SAA produced by macrophages promotes early lesion formation in the ascending aorta.
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spelling pubmed-46080702015-10-16 Serum Amyloid A Facilitates Early Lesion Development in Ldlr(−/−) Mice Krishack, Paulette A Bhanvadia, Clarissa V Lukens, John Sontag, Timothy J De Beer, Maria C Getz, Godfrey S Reardon, Catherine A J Am Heart Assoc Original Research BACKGROUND: Atherosclerosis is a chronic inflammatory disorder, and several studies have demonstrated a positive association between plasma serum amyloid A (SAA) levels and cardiovascular disease risk. The aim of the study was to examine whether SAA has a role in atherogenesis, the underlying basis of most cardiovascular disease. METHODS AND RESULTS: Mice globally deficient in acute-phase isoforms Saa1 and Saa2 (Saa(−/−)) were crossed to Ldlr(−/−) mice (Saa(−/−)Ldlr(−/−)). Saa(−/−)Ldlr(−/−) mice demonstrated a 31% reduction in lesional area in the ascending aorta but not in the aortic root or innominate artery after consuming a high-fat, high-cholesterol Western-type diet for 6 weeks. The lesions were predominantly macrophage foam cells. The phenotype was lost in more mature lesions in mice fed a Western-type diet for 12 weeks, suggesting that SAA is involved in early lesion development. The decreased atherosclerosis in the Saa(−/−)Ldlr(−/−) mice occurred despite increased levels of blood monocytes and was independent of plasma lipid levels. SAA is produced predominantly by hepatocytes and macrophages. To determine which source of SAA may have a dominant role in lesion development, bone marrow transplantation was performed. Ldlr(−/−) mice that received bone marrow from Saa(−/−)Ldlr(−/−) mice had slightly reduced ascending aorta atherosclerosis compared with Saa(−/−)Ldlr(−/−) mice receiving bone marrow from Ldlr(−/−) mice, indicating that the expression of SAA by macrophages may have an important influence on atherogenesis. CONCLUSIONS: The results indicate that SAA produced by macrophages promotes early lesion formation in the ascending aorta. John Wiley & Sons, Ltd 2015-07-17 /pmc/articles/PMC4608070/ /pubmed/26187995 http://dx.doi.org/10.1161/JAHA.115.001858 Text en © 2015 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research
Krishack, Paulette A
Bhanvadia, Clarissa V
Lukens, John
Sontag, Timothy J
De Beer, Maria C
Getz, Godfrey S
Reardon, Catherine A
Serum Amyloid A Facilitates Early Lesion Development in Ldlr(−/−) Mice
title Serum Amyloid A Facilitates Early Lesion Development in Ldlr(−/−) Mice
title_full Serum Amyloid A Facilitates Early Lesion Development in Ldlr(−/−) Mice
title_fullStr Serum Amyloid A Facilitates Early Lesion Development in Ldlr(−/−) Mice
title_full_unstemmed Serum Amyloid A Facilitates Early Lesion Development in Ldlr(−/−) Mice
title_short Serum Amyloid A Facilitates Early Lesion Development in Ldlr(−/−) Mice
title_sort serum amyloid a facilitates early lesion development in ldlr(−/−) mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608070/
https://www.ncbi.nlm.nih.gov/pubmed/26187995
http://dx.doi.org/10.1161/JAHA.115.001858
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