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Polarised fluid movement, and not cell death creates luminal spaces in adult prostate epithelium

There are two predominant theories for lumen formation in tissue morphogenesis; cavitation driven by cell death, and membrane separation driven by epithelial polarity. To define the mechanism of lumen formation in prostate acini we examined both theories in several cell lines grown in 3D Matrigel cu...

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Detalles Bibliográficos
Autores principales: Pearson, Joanna Frances, Hughes, Siobhan, Chambers, Karen, Lang, Shona Helen
Formato: Texto
Lenguaje:English
Publicado: 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2857323/
https://www.ncbi.nlm.nih.gov/pubmed/19096393
http://dx.doi.org/10.1038/cdd.2008.181
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author Pearson, Joanna Frances
Hughes, Siobhan
Chambers, Karen
Lang, Shona Helen
author_facet Pearson, Joanna Frances
Hughes, Siobhan
Chambers, Karen
Lang, Shona Helen
author_sort Pearson, Joanna Frances
collection PubMed
description There are two predominant theories for lumen formation in tissue morphogenesis; cavitation driven by cell death, and membrane separation driven by epithelial polarity. To define the mechanism of lumen formation in prostate acini we examined both theories in several cell lines grown in 3D Matrigel culture. Lumen formation occurred early in culture and preceded the expression of cell death markers for apoptosis (active caspase 3) and autophagy (LC-3). Active caspase 3 was expressed by very few cells and inhibition of apoptosis did not suppress lumen formation. Despite LC-3 expression in all cells within a spheroid, this was not associated with cell death. However, expression of the prostate secretory protein coincided with lumen formation and subsequent disruption of polarized fluid movement led to significant inhibition of lumen formation. This work indicates that lumen formation is driven by the polarized movement of fluids and proteins in 3D prostate epithelial models and not by cavitation.
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spelling pubmed-28573232010-04-20 Polarised fluid movement, and not cell death creates luminal spaces in adult prostate epithelium Pearson, Joanna Frances Hughes, Siobhan Chambers, Karen Lang, Shona Helen Cell Death Differ Article There are two predominant theories for lumen formation in tissue morphogenesis; cavitation driven by cell death, and membrane separation driven by epithelial polarity. To define the mechanism of lumen formation in prostate acini we examined both theories in several cell lines grown in 3D Matrigel culture. Lumen formation occurred early in culture and preceded the expression of cell death markers for apoptosis (active caspase 3) and autophagy (LC-3). Active caspase 3 was expressed by very few cells and inhibition of apoptosis did not suppress lumen formation. Despite LC-3 expression in all cells within a spheroid, this was not associated with cell death. However, expression of the prostate secretory protein coincided with lumen formation and subsequent disruption of polarized fluid movement led to significant inhibition of lumen formation. This work indicates that lumen formation is driven by the polarized movement of fluids and proteins in 3D prostate epithelial models and not by cavitation. 2008-12-19 2009-03 /pmc/articles/PMC2857323/ /pubmed/19096393 http://dx.doi.org/10.1038/cdd.2008.181 Text en
spellingShingle Article
Pearson, Joanna Frances
Hughes, Siobhan
Chambers, Karen
Lang, Shona Helen
Polarised fluid movement, and not cell death creates luminal spaces in adult prostate epithelium
title Polarised fluid movement, and not cell death creates luminal spaces in adult prostate epithelium
title_full Polarised fluid movement, and not cell death creates luminal spaces in adult prostate epithelium
title_fullStr Polarised fluid movement, and not cell death creates luminal spaces in adult prostate epithelium
title_full_unstemmed Polarised fluid movement, and not cell death creates luminal spaces in adult prostate epithelium
title_short Polarised fluid movement, and not cell death creates luminal spaces in adult prostate epithelium
title_sort polarised fluid movement, and not cell death creates luminal spaces in adult prostate epithelium
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2857323/
https://www.ncbi.nlm.nih.gov/pubmed/19096393
http://dx.doi.org/10.1038/cdd.2008.181
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