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IL-1α Mediated Chorioamnionitis Induces Depletion of FoxP3+ Cells and Ileal Inflammation in the Ovine Fetal Gut
BACKGROUND: Endotoxin induced chorioamnionitis increases IL-1 and provokes an inflammatory response in the fetal ileum that interferes with intestinal maturation. In the present study, we tested in an ovine chorioamnionitis model whether IL-1 is a major cytokine driving the inflammatory response in...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3066237/ https://www.ncbi.nlm.nih.gov/pubmed/21479249 http://dx.doi.org/10.1371/journal.pone.0018355 |
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author | Wolfs, Tim G. A. M. Kallapur, Suhas G. Polglase, Graeme R. Pillow, J. Jane Nitsos, Ilias Newnham, John P. Chougnet, Claire A. Kroon, Elke Spierings, Julia Willems, Coen H. M. P. Jobe, Alan H. Kramer, Boris W. |
author_facet | Wolfs, Tim G. A. M. Kallapur, Suhas G. Polglase, Graeme R. Pillow, J. Jane Nitsos, Ilias Newnham, John P. Chougnet, Claire A. Kroon, Elke Spierings, Julia Willems, Coen H. M. P. Jobe, Alan H. Kramer, Boris W. |
author_sort | Wolfs, Tim G. A. M. |
collection | PubMed |
description | BACKGROUND: Endotoxin induced chorioamnionitis increases IL-1 and provokes an inflammatory response in the fetal ileum that interferes with intestinal maturation. In the present study, we tested in an ovine chorioamnionitis model whether IL-1 is a major cytokine driving the inflammatory response in the fetal ileum. METHOD: Sheep bearing singleton fetuses received a single intraamniotic injection of recombinant ovine IL-1α at 7, 3 or 1 d before caesarian delivery at 125 days gestational age (term = 150 days). RESULTS: 3 and 7 d after IL-1α administration, intestinal mRNA levels for IL-4, IL-10, IFN-γ and TNF-α were strongly elevated. Numbers of CD3+ and CD4+ T-lymphocytes and myeloidperoxidase+ cells were increased whereas FoxP3+ T-cells were detected at low frequency. This increased proinflammatory state was associated with ileal mucosal barrier loss as demonstrated by decreased levels of the intestinal fatty acid binding protein and disruption of the tight junctional protein ZO-1. CONCLUSION: Intraamniotic IL-1α causes an acute detrimental inflammatory response in the ileum, suggesting that induction of IL-1 is a critical element in the pathophysiological effects of endotoxin induced chorioamnionitis. A disturbed balance between T-effector and FoxP3+ cells may contribute to this process. |
format | Text |
id | pubmed-3066237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30662372011-04-08 IL-1α Mediated Chorioamnionitis Induces Depletion of FoxP3+ Cells and Ileal Inflammation in the Ovine Fetal Gut Wolfs, Tim G. A. M. Kallapur, Suhas G. Polglase, Graeme R. Pillow, J. Jane Nitsos, Ilias Newnham, John P. Chougnet, Claire A. Kroon, Elke Spierings, Julia Willems, Coen H. M. P. Jobe, Alan H. Kramer, Boris W. PLoS One Research Article BACKGROUND: Endotoxin induced chorioamnionitis increases IL-1 and provokes an inflammatory response in the fetal ileum that interferes with intestinal maturation. In the present study, we tested in an ovine chorioamnionitis model whether IL-1 is a major cytokine driving the inflammatory response in the fetal ileum. METHOD: Sheep bearing singleton fetuses received a single intraamniotic injection of recombinant ovine IL-1α at 7, 3 or 1 d before caesarian delivery at 125 days gestational age (term = 150 days). RESULTS: 3 and 7 d after IL-1α administration, intestinal mRNA levels for IL-4, IL-10, IFN-γ and TNF-α were strongly elevated. Numbers of CD3+ and CD4+ T-lymphocytes and myeloidperoxidase+ cells were increased whereas FoxP3+ T-cells were detected at low frequency. This increased proinflammatory state was associated with ileal mucosal barrier loss as demonstrated by decreased levels of the intestinal fatty acid binding protein and disruption of the tight junctional protein ZO-1. CONCLUSION: Intraamniotic IL-1α causes an acute detrimental inflammatory response in the ileum, suggesting that induction of IL-1 is a critical element in the pathophysiological effects of endotoxin induced chorioamnionitis. A disturbed balance between T-effector and FoxP3+ cells may contribute to this process. Public Library of Science 2011-03-29 /pmc/articles/PMC3066237/ /pubmed/21479249 http://dx.doi.org/10.1371/journal.pone.0018355 Text en Wolfs 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 Wolfs, Tim G. A. M. Kallapur, Suhas G. Polglase, Graeme R. Pillow, J. Jane Nitsos, Ilias Newnham, John P. Chougnet, Claire A. Kroon, Elke Spierings, Julia Willems, Coen H. M. P. Jobe, Alan H. Kramer, Boris W. IL-1α Mediated Chorioamnionitis Induces Depletion of FoxP3+ Cells and Ileal Inflammation in the Ovine Fetal Gut |
title | IL-1α Mediated Chorioamnionitis Induces Depletion of FoxP3+
Cells and Ileal Inflammation in the Ovine Fetal Gut |
title_full | IL-1α Mediated Chorioamnionitis Induces Depletion of FoxP3+
Cells and Ileal Inflammation in the Ovine Fetal Gut |
title_fullStr | IL-1α Mediated Chorioamnionitis Induces Depletion of FoxP3+
Cells and Ileal Inflammation in the Ovine Fetal Gut |
title_full_unstemmed | IL-1α Mediated Chorioamnionitis Induces Depletion of FoxP3+
Cells and Ileal Inflammation in the Ovine Fetal Gut |
title_short | IL-1α Mediated Chorioamnionitis Induces Depletion of FoxP3+
Cells and Ileal Inflammation in the Ovine Fetal Gut |
title_sort | il-1α mediated chorioamnionitis induces depletion of foxp3+
cells and ileal inflammation in the ovine fetal gut |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3066237/ https://www.ncbi.nlm.nih.gov/pubmed/21479249 http://dx.doi.org/10.1371/journal.pone.0018355 |
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