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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...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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2008
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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. |
format | Text |
id | pubmed-2857323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
record_format | MEDLINE/PubMed |
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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