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Breeding Strategy Determines Rupture Incidence in Post-Infarct Healing WARPing Cardiovascular Research
BACKGROUND: Von Willebrand A domain Related Protein (WARP), is a recently identified extracellular matrix protein. Based upon its involvement in matrix biology and its expression in the heart, we hypothesized that WARP regulates cardiac remodeling processes in the post-infarct healing process. METHO...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4583407/ https://www.ncbi.nlm.nih.gov/pubmed/26406320 http://dx.doi.org/10.1371/journal.pone.0139199 |
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author | Deckx, Sophie Carai, Paolo Bateman, John Heymans, Stephane Papageorgiou, Anna-Pia |
author_facet | Deckx, Sophie Carai, Paolo Bateman, John Heymans, Stephane Papageorgiou, Anna-Pia |
author_sort | Deckx, Sophie |
collection | PubMed |
description | BACKGROUND: Von Willebrand A domain Related Protein (WARP), is a recently identified extracellular matrix protein. Based upon its involvement in matrix biology and its expression in the heart, we hypothesized that WARP regulates cardiac remodeling processes in the post-infarct healing process. METHODS AND RESULTS: In the mouse model of myocardial infarction (MI), WARP expression increased in the infarcted area 3-days post-MI. In the healthy myocardium WARP localized with perlecan in the basement membrane, which was disrupted upon injury. In vitro studies showed high expression of WARP by cardiac fibroblasts, which further increases upon TGFβ stimulation. Furthermore, WARP expression correlated with aSMA and COL1 expression, markers of fibroblast to myofibroblast transition, in vivo and in vitro. Finally, WARP knockdown in vitro affected extra- and intracellular basic fibroblast growth factor production in myofibroblasts. To investigate the function for WARP in infarction healing, we performed an MI study in WARP knockout (KO) mice backcrossed more than 10 times on an Australian C57Bl/6-J background and bred in-house, and compared to wild type (WT) mice of the same C57Bl/6-J strain but of commercial European origin. WARP KO mice showed no mortality after MI, whereas 40% of the WT mice died due to cardiac rupture. However, when WARP KO mice were backcrossed on the European C57Bl/6-J background and bred heterozygous in-house, the previously seen protective effect in the WARP KO mice after MI was lost. Importantly, comparison of the cardiac response post-MI in WT mice bred heterozygous in-house versus commercially purchased WT mice revealed differences in cardiac rupture. CONCLUSION: These data demonstrate a redundant role for WARP in the wound healing process after MI but demonstrate that the continental/breeding/housing origin of mice of the same C57Bl6-J strain is critical in determining the susceptibility to cardiac rupture and stress the importance of using the correct littermate controls. |
format | Online Article Text |
id | pubmed-4583407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45834072015-10-02 Breeding Strategy Determines Rupture Incidence in Post-Infarct Healing WARPing Cardiovascular Research Deckx, Sophie Carai, Paolo Bateman, John Heymans, Stephane Papageorgiou, Anna-Pia PLoS One Research Article BACKGROUND: Von Willebrand A domain Related Protein (WARP), is a recently identified extracellular matrix protein. Based upon its involvement in matrix biology and its expression in the heart, we hypothesized that WARP regulates cardiac remodeling processes in the post-infarct healing process. METHODS AND RESULTS: In the mouse model of myocardial infarction (MI), WARP expression increased in the infarcted area 3-days post-MI. In the healthy myocardium WARP localized with perlecan in the basement membrane, which was disrupted upon injury. In vitro studies showed high expression of WARP by cardiac fibroblasts, which further increases upon TGFβ stimulation. Furthermore, WARP expression correlated with aSMA and COL1 expression, markers of fibroblast to myofibroblast transition, in vivo and in vitro. Finally, WARP knockdown in vitro affected extra- and intracellular basic fibroblast growth factor production in myofibroblasts. To investigate the function for WARP in infarction healing, we performed an MI study in WARP knockout (KO) mice backcrossed more than 10 times on an Australian C57Bl/6-J background and bred in-house, and compared to wild type (WT) mice of the same C57Bl/6-J strain but of commercial European origin. WARP KO mice showed no mortality after MI, whereas 40% of the WT mice died due to cardiac rupture. However, when WARP KO mice were backcrossed on the European C57Bl/6-J background and bred heterozygous in-house, the previously seen protective effect in the WARP KO mice after MI was lost. Importantly, comparison of the cardiac response post-MI in WT mice bred heterozygous in-house versus commercially purchased WT mice revealed differences in cardiac rupture. CONCLUSION: These data demonstrate a redundant role for WARP in the wound healing process after MI but demonstrate that the continental/breeding/housing origin of mice of the same C57Bl6-J strain is critical in determining the susceptibility to cardiac rupture and stress the importance of using the correct littermate controls. Public Library of Science 2015-09-25 /pmc/articles/PMC4583407/ /pubmed/26406320 http://dx.doi.org/10.1371/journal.pone.0139199 Text en © 2015 Deckx et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Deckx, Sophie Carai, Paolo Bateman, John Heymans, Stephane Papageorgiou, Anna-Pia Breeding Strategy Determines Rupture Incidence in Post-Infarct Healing WARPing Cardiovascular Research |
title | Breeding Strategy Determines Rupture Incidence in Post-Infarct Healing WARPing Cardiovascular Research |
title_full | Breeding Strategy Determines Rupture Incidence in Post-Infarct Healing WARPing Cardiovascular Research |
title_fullStr | Breeding Strategy Determines Rupture Incidence in Post-Infarct Healing WARPing Cardiovascular Research |
title_full_unstemmed | Breeding Strategy Determines Rupture Incidence in Post-Infarct Healing WARPing Cardiovascular Research |
title_short | Breeding Strategy Determines Rupture Incidence in Post-Infarct Healing WARPing Cardiovascular Research |
title_sort | breeding strategy determines rupture incidence in post-infarct healing warping cardiovascular research |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4583407/ https://www.ncbi.nlm.nih.gov/pubmed/26406320 http://dx.doi.org/10.1371/journal.pone.0139199 |
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