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GDF-15 protects from macrophage accumulation in a mousemodel of advanced atherosclerosis

BACKGROUND: The cytokine growth differentiation factor-15 (GDF-15), a member of the TGF beta superfamily, has recently been discovered to play an important role in cardiovascular diseases. It is mostly expressed in macrophages of atherosclerotic lesions, but its impact on advanced atherosclerosis is...

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Autores principales: Preusch, Michael R, Baeuerle, Matthias, Albrecht, Claudia, Blessing, Erwin, Bischof, Marc, Katus, Hugo A, Bea, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701574/
https://www.ncbi.nlm.nih.gov/pubmed/23800095
http://dx.doi.org/10.1186/2047-783X-18-19
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author Preusch, Michael R
Baeuerle, Matthias
Albrecht, Claudia
Blessing, Erwin
Bischof, Marc
Katus, Hugo A
Bea, Florian
author_facet Preusch, Michael R
Baeuerle, Matthias
Albrecht, Claudia
Blessing, Erwin
Bischof, Marc
Katus, Hugo A
Bea, Florian
author_sort Preusch, Michael R
collection PubMed
description BACKGROUND: The cytokine growth differentiation factor-15 (GDF-15), a member of the TGF beta superfamily, has recently been discovered to play an important role in cardiovascular diseases. It is mostly expressed in macrophages of atherosclerotic lesions, but its impact on advanced atherosclerosis is still unknown. This study was performed to evaluate the effects of GDF-15 in an established mouse model of advanced atherosclerosis. METHODS: Thirty-eight LDL receptor deficient mice received a lethal body radiation. Half of the group was transplanted with bone marrow of GDF-15 deficient mice. Nineteen mice were transplanted with bone marrow from wild-type controls. After 24 weeks on an atherogenic diet, animals were euthanized and sections of the aortic sinus were prepared. Lesion size and lesion composition, as well as macrophage content,were evaluated. RESULTS: While demonstrating no difference in lesion size, LDL-receptor knockout mice transplanted with bone marrow from GDF-15 deficient mice showed enhanced macrophage accumulation and features of atherosclerotic plaque destabilization, such as thinning of fibrous caps. Immunostaining against intercellular adhesion molecule-1 further revealed an increased expression in mice receiving GDF-15-deficient bone marrow. CONCLUSIONS: This is the first study that demonstrates a protective role of GDF-15 in advanced atherosclerosis and macrophage accumulation, possibly due to the reduced expression of adhesion molecules.
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spelling pubmed-37015742013-07-05 GDF-15 protects from macrophage accumulation in a mousemodel of advanced atherosclerosis Preusch, Michael R Baeuerle, Matthias Albrecht, Claudia Blessing, Erwin Bischof, Marc Katus, Hugo A Bea, Florian Eur J Med Res Research BACKGROUND: The cytokine growth differentiation factor-15 (GDF-15), a member of the TGF beta superfamily, has recently been discovered to play an important role in cardiovascular diseases. It is mostly expressed in macrophages of atherosclerotic lesions, but its impact on advanced atherosclerosis is still unknown. This study was performed to evaluate the effects of GDF-15 in an established mouse model of advanced atherosclerosis. METHODS: Thirty-eight LDL receptor deficient mice received a lethal body radiation. Half of the group was transplanted with bone marrow of GDF-15 deficient mice. Nineteen mice were transplanted with bone marrow from wild-type controls. After 24 weeks on an atherogenic diet, animals were euthanized and sections of the aortic sinus were prepared. Lesion size and lesion composition, as well as macrophage content,were evaluated. RESULTS: While demonstrating no difference in lesion size, LDL-receptor knockout mice transplanted with bone marrow from GDF-15 deficient mice showed enhanced macrophage accumulation and features of atherosclerotic plaque destabilization, such as thinning of fibrous caps. Immunostaining against intercellular adhesion molecule-1 further revealed an increased expression in mice receiving GDF-15-deficient bone marrow. CONCLUSIONS: This is the first study that demonstrates a protective role of GDF-15 in advanced atherosclerosis and macrophage accumulation, possibly due to the reduced expression of adhesion molecules. BioMed Central 2013-06-24 /pmc/articles/PMC3701574/ /pubmed/23800095 http://dx.doi.org/10.1186/2047-783X-18-19 Text en Copyright © 2013 Preusch 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
Preusch, Michael R
Baeuerle, Matthias
Albrecht, Claudia
Blessing, Erwin
Bischof, Marc
Katus, Hugo A
Bea, Florian
GDF-15 protects from macrophage accumulation in a mousemodel of advanced atherosclerosis
title GDF-15 protects from macrophage accumulation in a mousemodel of advanced atherosclerosis
title_full GDF-15 protects from macrophage accumulation in a mousemodel of advanced atherosclerosis
title_fullStr GDF-15 protects from macrophage accumulation in a mousemodel of advanced atherosclerosis
title_full_unstemmed GDF-15 protects from macrophage accumulation in a mousemodel of advanced atherosclerosis
title_short GDF-15 protects from macrophage accumulation in a mousemodel of advanced atherosclerosis
title_sort gdf-15 protects from macrophage accumulation in a mousemodel of advanced atherosclerosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701574/
https://www.ncbi.nlm.nih.gov/pubmed/23800095
http://dx.doi.org/10.1186/2047-783X-18-19
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