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Trauma induces overexpression of Cx43 in human fetal membrane defects

OBJECTIVE: We developed an in vitro model to examine whether trauma induces connexin 43 (Cx43) expression and collagen organisation in the amniotic membrane (AM) of fetal membrane (FM) defects. METHOD: Term human FM was traumatised in vitro. Cell morphology and Cx43 were examined in the wound edge A...

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Autores principales: Barrett, David W., Kethees, Aumie, Thrasivoulou, Christopher, Mata, Alvaro, Virasami, Alex, Sebire, Neil J., Engels, Alex C., Deprest, Jan A., Becker, David L., David, Anna L., Chowdhury, Tina T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638101/
https://www.ncbi.nlm.nih.gov/pubmed/28664994
http://dx.doi.org/10.1002/pd.5104
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author Barrett, David W.
Kethees, Aumie
Thrasivoulou, Christopher
Mata, Alvaro
Virasami, Alex
Sebire, Neil J.
Engels, Alex C.
Deprest, Jan A.
Becker, David L.
David, Anna L.
Chowdhury, Tina T.
author_facet Barrett, David W.
Kethees, Aumie
Thrasivoulou, Christopher
Mata, Alvaro
Virasami, Alex
Sebire, Neil J.
Engels, Alex C.
Deprest, Jan A.
Becker, David L.
David, Anna L.
Chowdhury, Tina T.
author_sort Barrett, David W.
collection PubMed
description OBJECTIVE: We developed an in vitro model to examine whether trauma induces connexin 43 (Cx43) expression and collagen organisation in the amniotic membrane (AM) of fetal membrane (FM) defects. METHOD: Term human FM was traumatised in vitro. Cell morphology and Cx43 were examined in the wound edge AM by immunofluorescence (IMF) confocal microscopy and compared to control AM. Collagen microstructure was examined by second harmonic generation (SHG) imaging. Cell viability was assessed with calcein and ethidium staining. RESULTS: After trauma, the AM showed a dense region of cells, which had migrated towards the wound edge. In wound edge AM, Cx43 puncta was preferentially distributed in mesenchymal cells compared to epithelial cells with significant expression in the fibroblast layer than epithelial layer (p < 0.001). In the fibroblast layer, the collagen fibres were highly polarised and aligned in parallel to the axis of the wound edge AM. There was an absence of cell migration across the defect with no healing after 168 h. Cell viability of the FM after trauma was maintained during culture. CONCLUSION: Cx43 overexpression in wounded AM drives structural changes in collagen that slows down efficacy of cell migration across the FM defect. © 2017 The Authors. Prenatal Diagnosis published by John Wiley & Sons, Ltd.
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spelling pubmed-56381012017-10-25 Trauma induces overexpression of Cx43 in human fetal membrane defects Barrett, David W. Kethees, Aumie Thrasivoulou, Christopher Mata, Alvaro Virasami, Alex Sebire, Neil J. Engels, Alex C. Deprest, Jan A. Becker, David L. David, Anna L. Chowdhury, Tina T. Prenat Diagn Original Articles OBJECTIVE: We developed an in vitro model to examine whether trauma induces connexin 43 (Cx43) expression and collagen organisation in the amniotic membrane (AM) of fetal membrane (FM) defects. METHOD: Term human FM was traumatised in vitro. Cell morphology and Cx43 were examined in the wound edge AM by immunofluorescence (IMF) confocal microscopy and compared to control AM. Collagen microstructure was examined by second harmonic generation (SHG) imaging. Cell viability was assessed with calcein and ethidium staining. RESULTS: After trauma, the AM showed a dense region of cells, which had migrated towards the wound edge. In wound edge AM, Cx43 puncta was preferentially distributed in mesenchymal cells compared to epithelial cells with significant expression in the fibroblast layer than epithelial layer (p < 0.001). In the fibroblast layer, the collagen fibres were highly polarised and aligned in parallel to the axis of the wound edge AM. There was an absence of cell migration across the defect with no healing after 168 h. Cell viability of the FM after trauma was maintained during culture. CONCLUSION: Cx43 overexpression in wounded AM drives structural changes in collagen that slows down efficacy of cell migration across the FM defect. © 2017 The Authors. Prenatal Diagnosis published by John Wiley & Sons, Ltd. John Wiley and Sons Inc. 2017-08-01 2017-09 /pmc/articles/PMC5638101/ /pubmed/28664994 http://dx.doi.org/10.1002/pd.5104 Text en © 2017 The Authors. Prenatal Diagnosis published by John Wiley & Sons, Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Barrett, David W.
Kethees, Aumie
Thrasivoulou, Christopher
Mata, Alvaro
Virasami, Alex
Sebire, Neil J.
Engels, Alex C.
Deprest, Jan A.
Becker, David L.
David, Anna L.
Chowdhury, Tina T.
Trauma induces overexpression of Cx43 in human fetal membrane defects
title Trauma induces overexpression of Cx43 in human fetal membrane defects
title_full Trauma induces overexpression of Cx43 in human fetal membrane defects
title_fullStr Trauma induces overexpression of Cx43 in human fetal membrane defects
title_full_unstemmed Trauma induces overexpression of Cx43 in human fetal membrane defects
title_short Trauma induces overexpression of Cx43 in human fetal membrane defects
title_sort trauma induces overexpression of cx43 in human fetal membrane defects
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638101/
https://www.ncbi.nlm.nih.gov/pubmed/28664994
http://dx.doi.org/10.1002/pd.5104
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