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A bacterial encoded protein induces extreme multinucleation and cell-cell internalization in intestinal cells

Despite extensive study, the molecular mechanisms that lead to multinucleation and cell enlargement (hypertrophy) remain poorly understood. Here, we show that a single bacterial virulence protein, EspF, from the human pathogen enteropathogenic E. coli induces extreme multi-nucleation in small intest...

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Detalles Bibliográficos
Autores principales: Dean, Paul, Kenny, Brendan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3879132/
https://www.ncbi.nlm.nih.gov/pubmed/24665371
http://dx.doi.org/10.4161/tisb.22639
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author Dean, Paul
Kenny, Brendan
author_facet Dean, Paul
Kenny, Brendan
author_sort Dean, Paul
collection PubMed
description Despite extensive study, the molecular mechanisms that lead to multinucleation and cell enlargement (hypertrophy) remain poorly understood. Here, we show that a single bacterial virulence protein, EspF, from the human pathogen enteropathogenic E. coli induces extreme multi-nucleation in small intestinal epithelial cells. Ectopic expression of EspF induced cell-cell internalization events, presumably responsible for the enlarged multinucleated cells. These extreme phenotypes were dependent on a C-terminal polyproline-rich domain in EspF and not linked to the targeting of mitochondria or the nucleolus. The subversive functions of EspF may provide valuable insight into the molecular mechanisms that mediate cell fusion, multinucleation and cell hypertrophy.
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spelling pubmed-38791322014-02-19 A bacterial encoded protein induces extreme multinucleation and cell-cell internalization in intestinal cells Dean, Paul Kenny, Brendan Tissue Barriers Short Communication Despite extensive study, the molecular mechanisms that lead to multinucleation and cell enlargement (hypertrophy) remain poorly understood. Here, we show that a single bacterial virulence protein, EspF, from the human pathogen enteropathogenic E. coli induces extreme multi-nucleation in small intestinal epithelial cells. Ectopic expression of EspF induced cell-cell internalization events, presumably responsible for the enlarged multinucleated cells. These extreme phenotypes were dependent on a C-terminal polyproline-rich domain in EspF and not linked to the targeting of mitochondria or the nucleolus. The subversive functions of EspF may provide valuable insight into the molecular mechanisms that mediate cell fusion, multinucleation and cell hypertrophy. Landes Bioscience 2013-01-01 2013-01-01 /pmc/articles/PMC3879132/ /pubmed/24665371 http://dx.doi.org/10.4161/tisb.22639 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Short Communication
Dean, Paul
Kenny, Brendan
A bacterial encoded protein induces extreme multinucleation and cell-cell internalization in intestinal cells
title A bacterial encoded protein induces extreme multinucleation and cell-cell internalization in intestinal cells
title_full A bacterial encoded protein induces extreme multinucleation and cell-cell internalization in intestinal cells
title_fullStr A bacterial encoded protein induces extreme multinucleation and cell-cell internalization in intestinal cells
title_full_unstemmed A bacterial encoded protein induces extreme multinucleation and cell-cell internalization in intestinal cells
title_short A bacterial encoded protein induces extreme multinucleation and cell-cell internalization in intestinal cells
title_sort bacterial encoded protein induces extreme multinucleation and cell-cell internalization in intestinal cells
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3879132/
https://www.ncbi.nlm.nih.gov/pubmed/24665371
http://dx.doi.org/10.4161/tisb.22639
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