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Deficiency of the BMP Type I receptor ALK3 partly protects mice from anemia of inflammation
BACKGROUND: Inflammatory stimuli induce the hepatic iron regulatory hormone hepcidin, which contributes to anaemia of inflammation (AI). Hepcidin expression is regulated by the bone morphogenetic protein (BMP) and the interleukin-6 (IL-6) signalling pathways. Prior results indicate that the BMP type...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389079/ https://www.ncbi.nlm.nih.gov/pubmed/29482530 http://dx.doi.org/10.1186/s12899-018-0037-z |
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author | Gallitz, Inka Lofruthe, Niklas Traeger, Lisa Bäumer, Nicole Hoerr, Verena Faber, Cornelius Kuhlmann, Tanja Müller-Tidow, Carsten Steinbicker, Andrea U. |
author_facet | Gallitz, Inka Lofruthe, Niklas Traeger, Lisa Bäumer, Nicole Hoerr, Verena Faber, Cornelius Kuhlmann, Tanja Müller-Tidow, Carsten Steinbicker, Andrea U. |
author_sort | Gallitz, Inka |
collection | PubMed |
description | BACKGROUND: Inflammatory stimuli induce the hepatic iron regulatory hormone hepcidin, which contributes to anaemia of inflammation (AI). Hepcidin expression is regulated by the bone morphogenetic protein (BMP) and the interleukin-6 (IL-6) signalling pathways. Prior results indicate that the BMP type I receptor ALK3 is mainly involved in the acute inflammatory hepcidin induction four and 72 h after IL-6 administration. In this study, the role of ALK3 in a chronic model of inflammation was investigated. The intact, heat-killed bacterium Brucella abortus (BA) was used to analyse its effect on the development of inflammation and hypoferremia in mice with hepatocyte-specific Alk3-deficiency (Alk3(fl/fl); Alb-Cre) compared to control (Alk3(fl/fl)) mice. RESULTS: An iron restricted diet prevented development of the iron overload phenotype in mice with hepatocyte-specific Alk3 deficiency. Regular diet leads to iron overload and increased haemoglobin levels in these mice, which protects from the development of AI per se. Fourteen days after BA injection Alk3(fl/fl); Alb-Cre mice presented milder anaemia (Hb 16.7 g/dl to 11.6 g/dl) compared to Alk3(fl/fl) control mice (Hb 14.9 g/dl to 8.6 g/dl). BA injection led to an intact inflammatory response in all groups of mice. In Alk3(fl/fl); Alb-Cre mice, SMAD1/5/8 phosphorylation was reduced after BA as well as after infection with Staphylococcus aureus. The reduction of the SMAD1/5/8 signalling pathway due to hepatocyte-specific Alk3 deficiency partly suppressed the induction of STAT3 signalling. CONCLUSION: The results reveal in vivo, that 1) hepatocyte-specific Alk3 deficiency partly protects from AI, 2) the development of hypoferremia is partly dependent on ALK3, and 3) the ALK3/BMP/hepcidin axis may serve as a possible therapeutic target to attenuate AI. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12899-018-0037-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6389079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63890792019-03-19 Deficiency of the BMP Type I receptor ALK3 partly protects mice from anemia of inflammation Gallitz, Inka Lofruthe, Niklas Traeger, Lisa Bäumer, Nicole Hoerr, Verena Faber, Cornelius Kuhlmann, Tanja Müller-Tidow, Carsten Steinbicker, Andrea U. BMC Physiol Research Article BACKGROUND: Inflammatory stimuli induce the hepatic iron regulatory hormone hepcidin, which contributes to anaemia of inflammation (AI). Hepcidin expression is regulated by the bone morphogenetic protein (BMP) and the interleukin-6 (IL-6) signalling pathways. Prior results indicate that the BMP type I receptor ALK3 is mainly involved in the acute inflammatory hepcidin induction four and 72 h after IL-6 administration. In this study, the role of ALK3 in a chronic model of inflammation was investigated. The intact, heat-killed bacterium Brucella abortus (BA) was used to analyse its effect on the development of inflammation and hypoferremia in mice with hepatocyte-specific Alk3-deficiency (Alk3(fl/fl); Alb-Cre) compared to control (Alk3(fl/fl)) mice. RESULTS: An iron restricted diet prevented development of the iron overload phenotype in mice with hepatocyte-specific Alk3 deficiency. Regular diet leads to iron overload and increased haemoglobin levels in these mice, which protects from the development of AI per se. Fourteen days after BA injection Alk3(fl/fl); Alb-Cre mice presented milder anaemia (Hb 16.7 g/dl to 11.6 g/dl) compared to Alk3(fl/fl) control mice (Hb 14.9 g/dl to 8.6 g/dl). BA injection led to an intact inflammatory response in all groups of mice. In Alk3(fl/fl); Alb-Cre mice, SMAD1/5/8 phosphorylation was reduced after BA as well as after infection with Staphylococcus aureus. The reduction of the SMAD1/5/8 signalling pathway due to hepatocyte-specific Alk3 deficiency partly suppressed the induction of STAT3 signalling. CONCLUSION: The results reveal in vivo, that 1) hepatocyte-specific Alk3 deficiency partly protects from AI, 2) the development of hypoferremia is partly dependent on ALK3, and 3) the ALK3/BMP/hepcidin axis may serve as a possible therapeutic target to attenuate AI. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12899-018-0037-z) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-27 /pmc/articles/PMC6389079/ /pubmed/29482530 http://dx.doi.org/10.1186/s12899-018-0037-z 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 | Research Article Gallitz, Inka Lofruthe, Niklas Traeger, Lisa Bäumer, Nicole Hoerr, Verena Faber, Cornelius Kuhlmann, Tanja Müller-Tidow, Carsten Steinbicker, Andrea U. Deficiency of the BMP Type I receptor ALK3 partly protects mice from anemia of inflammation |
title | Deficiency of the BMP Type I receptor ALK3 partly protects mice from anemia of inflammation |
title_full | Deficiency of the BMP Type I receptor ALK3 partly protects mice from anemia of inflammation |
title_fullStr | Deficiency of the BMP Type I receptor ALK3 partly protects mice from anemia of inflammation |
title_full_unstemmed | Deficiency of the BMP Type I receptor ALK3 partly protects mice from anemia of inflammation |
title_short | Deficiency of the BMP Type I receptor ALK3 partly protects mice from anemia of inflammation |
title_sort | deficiency of the bmp type i receptor alk3 partly protects mice from anemia of inflammation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389079/ https://www.ncbi.nlm.nih.gov/pubmed/29482530 http://dx.doi.org/10.1186/s12899-018-0037-z |
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