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High density lipoprotein cholesterol and proteome in SR-B1 KO mice: lost in precipitation

Scavenger receptor class B type 1 (SR-B1) plays an essential role in high density lipoprotein (HDL) metabolism. SR-B1 deficient (SR-B1 KO) mice are prone to atherosclerosis and exhibit abnormally large, cholesterol-rich, dysfunctional HDL. In a recent issue of J Transl Med, Cao et al. described resu...

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Autores principales: Contreras-Duarte, Susana, Santander, Nicolás, Birner-Gruenberger, Ruth, Wadsack, Christian, Rigotti, Attilio, Busso, Dolores
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233513/
https://www.ncbi.nlm.nih.gov/pubmed/30419936
http://dx.doi.org/10.1186/s12967-018-1683-4
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author Contreras-Duarte, Susana
Santander, Nicolás
Birner-Gruenberger, Ruth
Wadsack, Christian
Rigotti, Attilio
Busso, Dolores
author_facet Contreras-Duarte, Susana
Santander, Nicolás
Birner-Gruenberger, Ruth
Wadsack, Christian
Rigotti, Attilio
Busso, Dolores
author_sort Contreras-Duarte, Susana
collection PubMed
description Scavenger receptor class B type 1 (SR-B1) plays an essential role in high density lipoprotein (HDL) metabolism. SR-B1 deficient (SR-B1 KO) mice are prone to atherosclerosis and exhibit abnormally large, cholesterol-rich, dysfunctional HDL. In a recent issue of J Transl Med, Cao et al. described results of proteomics analyses of HDL isolated from wild-type (WT) and SR-B1 KO mice using precipitation of large lipoproteins with polyethylene glycol (PEG). They report abnormalities in SR-B1 KO HDL protein components that correlate with HDL function. In this commentary, we describe and discuss the differences in the results published by Cao et al. and those obtained in a recent study from our laboratory using shotgun proteomics of HDL of SR-B1 KO mice isolated by ultracentrifugation. We propose that different HDL purification procedures used may account for the discrepancies observed. We show that SR-B1 KO HDL purification using either PEG or dextran sulfate precipitation results in enrichment of small HDL subclasses, and may therefore underestimate alterations in lipoprotein composition or function. Compared to HDL obtained by ultracentrifugation, HDL isolated by PEG precipitation show a lower ApoE/ApoA-I proportion and reduced cholesterol content. HDL protein components described by Cao et al. or our laboratory are mostly inconsistent: only 33 HDL proteins were detected in both datasets, whereas a significant number of proteins were only identified by Cao et al. (n = 43) or Contreras-Duarte et al. (n = 26) datasets. The relative abundance of HDL-associated peptide and protein levels in WT vs SR-B1 HDL were also highly different in both datasets. This study indicates that caution must be taken when interpreting results from HDL isolated by chemical precipitation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12967-018-1683-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-62335132018-11-20 High density lipoprotein cholesterol and proteome in SR-B1 KO mice: lost in precipitation Contreras-Duarte, Susana Santander, Nicolás Birner-Gruenberger, Ruth Wadsack, Christian Rigotti, Attilio Busso, Dolores J Transl Med Commentary Scavenger receptor class B type 1 (SR-B1) plays an essential role in high density lipoprotein (HDL) metabolism. SR-B1 deficient (SR-B1 KO) mice are prone to atherosclerosis and exhibit abnormally large, cholesterol-rich, dysfunctional HDL. In a recent issue of J Transl Med, Cao et al. described results of proteomics analyses of HDL isolated from wild-type (WT) and SR-B1 KO mice using precipitation of large lipoproteins with polyethylene glycol (PEG). They report abnormalities in SR-B1 KO HDL protein components that correlate with HDL function. In this commentary, we describe and discuss the differences in the results published by Cao et al. and those obtained in a recent study from our laboratory using shotgun proteomics of HDL of SR-B1 KO mice isolated by ultracentrifugation. We propose that different HDL purification procedures used may account for the discrepancies observed. We show that SR-B1 KO HDL purification using either PEG or dextran sulfate precipitation results in enrichment of small HDL subclasses, and may therefore underestimate alterations in lipoprotein composition or function. Compared to HDL obtained by ultracentrifugation, HDL isolated by PEG precipitation show a lower ApoE/ApoA-I proportion and reduced cholesterol content. HDL protein components described by Cao et al. or our laboratory are mostly inconsistent: only 33 HDL proteins were detected in both datasets, whereas a significant number of proteins were only identified by Cao et al. (n = 43) or Contreras-Duarte et al. (n = 26) datasets. The relative abundance of HDL-associated peptide and protein levels in WT vs SR-B1 HDL were also highly different in both datasets. This study indicates that caution must be taken when interpreting results from HDL isolated by chemical precipitation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12967-018-1683-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-12 /pmc/articles/PMC6233513/ /pubmed/30419936 http://dx.doi.org/10.1186/s12967-018-1683-4 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Commentary
Contreras-Duarte, Susana
Santander, Nicolás
Birner-Gruenberger, Ruth
Wadsack, Christian
Rigotti, Attilio
Busso, Dolores
High density lipoprotein cholesterol and proteome in SR-B1 KO mice: lost in precipitation
title High density lipoprotein cholesterol and proteome in SR-B1 KO mice: lost in precipitation
title_full High density lipoprotein cholesterol and proteome in SR-B1 KO mice: lost in precipitation
title_fullStr High density lipoprotein cholesterol and proteome in SR-B1 KO mice: lost in precipitation
title_full_unstemmed High density lipoprotein cholesterol and proteome in SR-B1 KO mice: lost in precipitation
title_short High density lipoprotein cholesterol and proteome in SR-B1 KO mice: lost in precipitation
title_sort high density lipoprotein cholesterol and proteome in sr-b1 ko mice: lost in precipitation
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233513/
https://www.ncbi.nlm.nih.gov/pubmed/30419936
http://dx.doi.org/10.1186/s12967-018-1683-4
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