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The effect of human amnion epithelial cells on lung development and inflammation in preterm lambs exposed to antenatal inflammation

BACKGROUND: Lung inflammation and impaired alveolarization are hallmarks of bronchopulmonary dysplasia (BPD). We hypothesize that human amnion epithelial cells (hAECs) are anti-inflammatory and reduce lung injury in preterm lambs born after antenatal exposure to inflammation. METHODS: Pregnant ewes...

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Autores principales: Papagianis, Paris Clarice, Ahmadi-Noorbakhsh, Siavash, Lim, Rebecca, Wallace, Euan, Polglase, Graeme, Pillow, J. Jane, Moss, Timothy J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232434/
https://www.ncbi.nlm.nih.gov/pubmed/34170941
http://dx.doi.org/10.1371/journal.pone.0253456
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author Papagianis, Paris Clarice
Ahmadi-Noorbakhsh, Siavash
Lim, Rebecca
Wallace, Euan
Polglase, Graeme
Pillow, J. Jane
Moss, Timothy J.
author_facet Papagianis, Paris Clarice
Ahmadi-Noorbakhsh, Siavash
Lim, Rebecca
Wallace, Euan
Polglase, Graeme
Pillow, J. Jane
Moss, Timothy J.
author_sort Papagianis, Paris Clarice
collection PubMed
description BACKGROUND: Lung inflammation and impaired alveolarization are hallmarks of bronchopulmonary dysplasia (BPD). We hypothesize that human amnion epithelial cells (hAECs) are anti-inflammatory and reduce lung injury in preterm lambs born after antenatal exposure to inflammation. METHODS: Pregnant ewes received either intra-amniotic lipopolysaccharide (LPS, from E.coli 055:B5; 4mg) or saline (Sal) on day 126 of gestation. Lambs were delivered by cesarean section at 128 d gestation (term ~150 d). Lambs received intravenous hAECs (LPS/hAECs: n = 7; 30x10(6) cells) or equivalent volumes of saline (LPS/Sal, n = 10; or Sal/Sal, n = 9) immediately after birth. Respiratory support was gradually de-escalated, aimed at early weaning from mechanical ventilation towards unassisted respiration. Lung tissue was collected 1 week after birth. Lung morphology was assessed and mRNA levels for inflammatory mediators were measured. RESULTS: Respiratory support required by LPS/hAEC lambs was not different to Sal/Sal or LPS/Sal lambs. Lung tissue:airspace ratio was lower in the LPS/Sal compared to Sal/Sal lambs (P<0.05), but not LPS/hAEC lambs. LPS/hAEC lambs tended to have increased septation in their lungs versus LPS/Sal (P = 0.08). Expression of inflammatory cytokines was highest in LPS/hAECs lambs. CONCLUSIONS: Postnatal administration of a single dose of hAECs stimulates a pulmonary immune response without changing ventilator requirements in preterm lambs born after intrauterine inflammation.
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spelling pubmed-82324342021-07-07 The effect of human amnion epithelial cells on lung development and inflammation in preterm lambs exposed to antenatal inflammation Papagianis, Paris Clarice Ahmadi-Noorbakhsh, Siavash Lim, Rebecca Wallace, Euan Polglase, Graeme Pillow, J. Jane Moss, Timothy J. PLoS One Research Article BACKGROUND: Lung inflammation and impaired alveolarization are hallmarks of bronchopulmonary dysplasia (BPD). We hypothesize that human amnion epithelial cells (hAECs) are anti-inflammatory and reduce lung injury in preterm lambs born after antenatal exposure to inflammation. METHODS: Pregnant ewes received either intra-amniotic lipopolysaccharide (LPS, from E.coli 055:B5; 4mg) or saline (Sal) on day 126 of gestation. Lambs were delivered by cesarean section at 128 d gestation (term ~150 d). Lambs received intravenous hAECs (LPS/hAECs: n = 7; 30x10(6) cells) or equivalent volumes of saline (LPS/Sal, n = 10; or Sal/Sal, n = 9) immediately after birth. Respiratory support was gradually de-escalated, aimed at early weaning from mechanical ventilation towards unassisted respiration. Lung tissue was collected 1 week after birth. Lung morphology was assessed and mRNA levels for inflammatory mediators were measured. RESULTS: Respiratory support required by LPS/hAEC lambs was not different to Sal/Sal or LPS/Sal lambs. Lung tissue:airspace ratio was lower in the LPS/Sal compared to Sal/Sal lambs (P<0.05), but not LPS/hAEC lambs. LPS/hAEC lambs tended to have increased septation in their lungs versus LPS/Sal (P = 0.08). Expression of inflammatory cytokines was highest in LPS/hAECs lambs. CONCLUSIONS: Postnatal administration of a single dose of hAECs stimulates a pulmonary immune response without changing ventilator requirements in preterm lambs born after intrauterine inflammation. Public Library of Science 2021-06-25 /pmc/articles/PMC8232434/ /pubmed/34170941 http://dx.doi.org/10.1371/journal.pone.0253456 Text en © 2021 Papagianis et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Papagianis, Paris Clarice
Ahmadi-Noorbakhsh, Siavash
Lim, Rebecca
Wallace, Euan
Polglase, Graeme
Pillow, J. Jane
Moss, Timothy J.
The effect of human amnion epithelial cells on lung development and inflammation in preterm lambs exposed to antenatal inflammation
title The effect of human amnion epithelial cells on lung development and inflammation in preterm lambs exposed to antenatal inflammation
title_full The effect of human amnion epithelial cells on lung development and inflammation in preterm lambs exposed to antenatal inflammation
title_fullStr The effect of human amnion epithelial cells on lung development and inflammation in preterm lambs exposed to antenatal inflammation
title_full_unstemmed The effect of human amnion epithelial cells on lung development and inflammation in preterm lambs exposed to antenatal inflammation
title_short The effect of human amnion epithelial cells on lung development and inflammation in preterm lambs exposed to antenatal inflammation
title_sort effect of human amnion epithelial cells on lung development and inflammation in preterm lambs exposed to antenatal inflammation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232434/
https://www.ncbi.nlm.nih.gov/pubmed/34170941
http://dx.doi.org/10.1371/journal.pone.0253456
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