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Apoproteins E, A-I, and SAA in Macrophage Pathobiology Related to Atherogenesis
Macrophages are core cellular elements of both early and advanced atherosclerosis. They take up modified lipoproteins and become lipid-loaded foam cells and secrete factors that influence other cell types in the artery wall involved in atherogenesis. Apoproteins E, AI, and SAA are all found on HDL w...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558525/ https://www.ncbi.nlm.nih.gov/pubmed/31231209 http://dx.doi.org/10.3389/fphar.2019.00536 |
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author | Getz, Godfrey S. Reardon, Catherine A. |
author_facet | Getz, Godfrey S. Reardon, Catherine A. |
author_sort | Getz, Godfrey S. |
collection | PubMed |
description | Macrophages are core cellular elements of both early and advanced atherosclerosis. They take up modified lipoproteins and become lipid-loaded foam cells and secrete factors that influence other cell types in the artery wall involved in atherogenesis. Apoproteins E, AI, and SAA are all found on HDL which can enter the artery wall. In addition, apoE is synthesized by macrophages. These three apoproteins can promote cholesterol efflux from lipid-loaded macrophages and have other functions that modulate macrophage biology. Mimetic peptides based on the sequence or structure of these apoproteins replicate some of these properties and are potential therapeutic agents for the treatment of atherosclerosis to reduce cardiovascular diseases. |
format | Online Article Text |
id | pubmed-6558525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65585252019-06-21 Apoproteins E, A-I, and SAA in Macrophage Pathobiology Related to Atherogenesis Getz, Godfrey S. Reardon, Catherine A. Front Pharmacol Pharmacology Macrophages are core cellular elements of both early and advanced atherosclerosis. They take up modified lipoproteins and become lipid-loaded foam cells and secrete factors that influence other cell types in the artery wall involved in atherogenesis. Apoproteins E, AI, and SAA are all found on HDL which can enter the artery wall. In addition, apoE is synthesized by macrophages. These three apoproteins can promote cholesterol efflux from lipid-loaded macrophages and have other functions that modulate macrophage biology. Mimetic peptides based on the sequence or structure of these apoproteins replicate some of these properties and are potential therapeutic agents for the treatment of atherosclerosis to reduce cardiovascular diseases. Frontiers Media S.A. 2019-05-21 /pmc/articles/PMC6558525/ /pubmed/31231209 http://dx.doi.org/10.3389/fphar.2019.00536 Text en Copyright © 2019 Getz and Reardon. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Getz, Godfrey S. Reardon, Catherine A. Apoproteins E, A-I, and SAA in Macrophage Pathobiology Related to Atherogenesis |
title | Apoproteins E, A-I, and SAA in Macrophage Pathobiology Related to Atherogenesis |
title_full | Apoproteins E, A-I, and SAA in Macrophage Pathobiology Related to Atherogenesis |
title_fullStr | Apoproteins E, A-I, and SAA in Macrophage Pathobiology Related to Atherogenesis |
title_full_unstemmed | Apoproteins E, A-I, and SAA in Macrophage Pathobiology Related to Atherogenesis |
title_short | Apoproteins E, A-I, and SAA in Macrophage Pathobiology Related to Atherogenesis |
title_sort | apoproteins e, a-i, and saa in macrophage pathobiology related to atherogenesis |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558525/ https://www.ncbi.nlm.nih.gov/pubmed/31231209 http://dx.doi.org/10.3389/fphar.2019.00536 |
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