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Presence of serum amyloid A3 in mouse plasma is dependent on the nature and extent of the inflammatory stimulus
Serum amyloid A3 (Saa3) derives mainly from extrahepatic tissue and is not detected in plasma from moderately inflamed obese mice. In contrast, it is present in plasma from mice acutely inflamed by injection of high dose of lipopolysaccharide (LPS). To reconcile these differences, we evaluated wheth...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7316782/ https://www.ncbi.nlm.nih.gov/pubmed/32587356 http://dx.doi.org/10.1038/s41598-020-66898-7 |
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author | Chait, Alan den Hartigh, Laura J. Wang, Shari Goodspeed, Leela Babenko, Ilona Altemeier, William A. Vaisar, Tomas |
author_facet | Chait, Alan den Hartigh, Laura J. Wang, Shari Goodspeed, Leela Babenko, Ilona Altemeier, William A. Vaisar, Tomas |
author_sort | Chait, Alan |
collection | PubMed |
description | Serum amyloid A3 (Saa3) derives mainly from extrahepatic tissue and is not detected in plasma from moderately inflamed obese mice. In contrast, it is present in plasma from mice acutely inflamed by injection of high dose of lipopolysaccharide (LPS). To reconcile these differences, we evaluated whether different acute inflammatory stimuli could affect the presence of Saa3 in plasma. Saa3 appeared dose dependently in plasma after LPS injection. In contrast, only very low levels were detected after sterile inflammation with silver nitrate despite levels of Saa1 and Saa2 being comparable to high dose LPS. Saa3 was not detected in plasma following casein administration. Although most Saa3 was found in HDL, a small amount was not lipoprotein associated. Gene expression and proteomic analysis of liver and adipose tissue suggested that a major source of Saa3 in plasma after injection of LPS was adipose tissue rather than liver. We conclude that Saa3 only appears in plasma after induction of acute inflammation by some but not all inflammatory stimuli. These findings are consistent with the observation that Saa3 is not detectable in plasma in more moderate chronic inflammatory states such as obesity. |
format | Online Article Text |
id | pubmed-7316782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73167822020-06-26 Presence of serum amyloid A3 in mouse plasma is dependent on the nature and extent of the inflammatory stimulus Chait, Alan den Hartigh, Laura J. Wang, Shari Goodspeed, Leela Babenko, Ilona Altemeier, William A. Vaisar, Tomas Sci Rep Article Serum amyloid A3 (Saa3) derives mainly from extrahepatic tissue and is not detected in plasma from moderately inflamed obese mice. In contrast, it is present in plasma from mice acutely inflamed by injection of high dose of lipopolysaccharide (LPS). To reconcile these differences, we evaluated whether different acute inflammatory stimuli could affect the presence of Saa3 in plasma. Saa3 appeared dose dependently in plasma after LPS injection. In contrast, only very low levels were detected after sterile inflammation with silver nitrate despite levels of Saa1 and Saa2 being comparable to high dose LPS. Saa3 was not detected in plasma following casein administration. Although most Saa3 was found in HDL, a small amount was not lipoprotein associated. Gene expression and proteomic analysis of liver and adipose tissue suggested that a major source of Saa3 in plasma after injection of LPS was adipose tissue rather than liver. We conclude that Saa3 only appears in plasma after induction of acute inflammation by some but not all inflammatory stimuli. These findings are consistent with the observation that Saa3 is not detectable in plasma in more moderate chronic inflammatory states such as obesity. Nature Publishing Group UK 2020-06-25 /pmc/articles/PMC7316782/ /pubmed/32587356 http://dx.doi.org/10.1038/s41598-020-66898-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chait, Alan den Hartigh, Laura J. Wang, Shari Goodspeed, Leela Babenko, Ilona Altemeier, William A. Vaisar, Tomas Presence of serum amyloid A3 in mouse plasma is dependent on the nature and extent of the inflammatory stimulus |
title | Presence of serum amyloid A3 in mouse plasma is dependent on the nature and extent of the inflammatory stimulus |
title_full | Presence of serum amyloid A3 in mouse plasma is dependent on the nature and extent of the inflammatory stimulus |
title_fullStr | Presence of serum amyloid A3 in mouse plasma is dependent on the nature and extent of the inflammatory stimulus |
title_full_unstemmed | Presence of serum amyloid A3 in mouse plasma is dependent on the nature and extent of the inflammatory stimulus |
title_short | Presence of serum amyloid A3 in mouse plasma is dependent on the nature and extent of the inflammatory stimulus |
title_sort | presence of serum amyloid a3 in mouse plasma is dependent on the nature and extent of the inflammatory stimulus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7316782/ https://www.ncbi.nlm.nih.gov/pubmed/32587356 http://dx.doi.org/10.1038/s41598-020-66898-7 |
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