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Decreased APOE-containing HDL subfractions and cholesterol efflux capacity of serum in mice lacking Pcsk9
BACKGROUND: Studies in animals showed that PCSK9 is involved in HDL metabolism. We investigated the molecular mechanism by which PCSK9 regulates HDL cholesterol concentration and also whether Pcsk9 inactivation might affect cholesterol efflux capacity of serum and atherosclerotic fatty streak volume...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751695/ https://www.ncbi.nlm.nih.gov/pubmed/23883163 http://dx.doi.org/10.1186/1476-511X-12-112 |
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author | Choi, Seungbum Aljakna, Aleksandra Srivastava, Ujala Peterson, Blake R Deng, Bin Prat, Annik Korstanje, Ron |
author_facet | Choi, Seungbum Aljakna, Aleksandra Srivastava, Ujala Peterson, Blake R Deng, Bin Prat, Annik Korstanje, Ron |
author_sort | Choi, Seungbum |
collection | PubMed |
description | BACKGROUND: Studies in animals showed that PCSK9 is involved in HDL metabolism. We investigated the molecular mechanism by which PCSK9 regulates HDL cholesterol concentration and also whether Pcsk9 inactivation might affect cholesterol efflux capacity of serum and atherosclerotic fatty streak volume. METHODS: Mass spectrometry and western blot were used to analyze the level of apolipoprotein E (APOE) and A1 (APOA1). A mouse model overexpressing human LDLR was used to test the effect of high levels of liver LDLR on the concentration of HDL cholesterol and APOE-containing HDL subfractions. Pcsk9 knockout males lacking LDLR and APOE were used to test whether LDLR and APOE are necessary for PCSK9-mediated HDL cholesterol regulation. We also investigated the effects of Pcsk9 inactivation on cholesterol efflux capacity of serum using THP-1 and J774.A1 macrophage foam cells and atherosclerotic fatty streak volume in the aortic sinus of Pcsk9 knockout males fed an atherogenic diet. RESULTS: APOE and APOA1 were reduced in the same HDL subfractions of Pcsk9 knockout and human LDLR transgenic male mice. In Pcsk9/Ldlr double-knockout mice, HDL cholesterol concentration was lower than in Ldlr knockout mice and higher than in wild-type controls. In Pcsk9/Apoe double-knockout mice, HDL cholesterol concentration was similar to that of Apoe knockout males. In Pcsk9 knockout males, THP-1 macrophage cholesterol efflux capacity of serum was reduced and the fatty streak lesion volume was similar to wild-type controls. CONCLUSIONS: In mice, LDLR and APOE are important factors for PCSK9-mediated HDL regulation. Our data suggest that, although LDLR plays a major role in PCSK9-mediated regulation of HDL cholesterol concentration, it is not the only mechanism and that, regardless of mechanism, APOE is essential. Pcsk9 inactivation decreases the HDL cholesterol concentration and cholesterol efflux capacity in serum, but does not increase atherosclerotic fatty streak volume. |
format | Online Article Text |
id | pubmed-3751695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37516952013-08-24 Decreased APOE-containing HDL subfractions and cholesterol efflux capacity of serum in mice lacking Pcsk9 Choi, Seungbum Aljakna, Aleksandra Srivastava, Ujala Peterson, Blake R Deng, Bin Prat, Annik Korstanje, Ron Lipids Health Dis Research BACKGROUND: Studies in animals showed that PCSK9 is involved in HDL metabolism. We investigated the molecular mechanism by which PCSK9 regulates HDL cholesterol concentration and also whether Pcsk9 inactivation might affect cholesterol efflux capacity of serum and atherosclerotic fatty streak volume. METHODS: Mass spectrometry and western blot were used to analyze the level of apolipoprotein E (APOE) and A1 (APOA1). A mouse model overexpressing human LDLR was used to test the effect of high levels of liver LDLR on the concentration of HDL cholesterol and APOE-containing HDL subfractions. Pcsk9 knockout males lacking LDLR and APOE were used to test whether LDLR and APOE are necessary for PCSK9-mediated HDL cholesterol regulation. We also investigated the effects of Pcsk9 inactivation on cholesterol efflux capacity of serum using THP-1 and J774.A1 macrophage foam cells and atherosclerotic fatty streak volume in the aortic sinus of Pcsk9 knockout males fed an atherogenic diet. RESULTS: APOE and APOA1 were reduced in the same HDL subfractions of Pcsk9 knockout and human LDLR transgenic male mice. In Pcsk9/Ldlr double-knockout mice, HDL cholesterol concentration was lower than in Ldlr knockout mice and higher than in wild-type controls. In Pcsk9/Apoe double-knockout mice, HDL cholesterol concentration was similar to that of Apoe knockout males. In Pcsk9 knockout males, THP-1 macrophage cholesterol efflux capacity of serum was reduced and the fatty streak lesion volume was similar to wild-type controls. CONCLUSIONS: In mice, LDLR and APOE are important factors for PCSK9-mediated HDL regulation. Our data suggest that, although LDLR plays a major role in PCSK9-mediated regulation of HDL cholesterol concentration, it is not the only mechanism and that, regardless of mechanism, APOE is essential. Pcsk9 inactivation decreases the HDL cholesterol concentration and cholesterol efflux capacity in serum, but does not increase atherosclerotic fatty streak volume. BioMed Central 2013-07-24 /pmc/articles/PMC3751695/ /pubmed/23883163 http://dx.doi.org/10.1186/1476-511X-12-112 Text en Copyright © 2013 Choi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Choi, Seungbum Aljakna, Aleksandra Srivastava, Ujala Peterson, Blake R Deng, Bin Prat, Annik Korstanje, Ron Decreased APOE-containing HDL subfractions and cholesterol efflux capacity of serum in mice lacking Pcsk9 |
title | Decreased APOE-containing HDL subfractions and cholesterol efflux capacity of serum in mice lacking Pcsk9 |
title_full | Decreased APOE-containing HDL subfractions and cholesterol efflux capacity of serum in mice lacking Pcsk9 |
title_fullStr | Decreased APOE-containing HDL subfractions and cholesterol efflux capacity of serum in mice lacking Pcsk9 |
title_full_unstemmed | Decreased APOE-containing HDL subfractions and cholesterol efflux capacity of serum in mice lacking Pcsk9 |
title_short | Decreased APOE-containing HDL subfractions and cholesterol efflux capacity of serum in mice lacking Pcsk9 |
title_sort | decreased apoe-containing hdl subfractions and cholesterol efflux capacity of serum in mice lacking pcsk9 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751695/ https://www.ncbi.nlm.nih.gov/pubmed/23883163 http://dx.doi.org/10.1186/1476-511X-12-112 |
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