Adenoviral vectors stimulate glucagon transcription in human mesenchymal stem cells expressing pancreatic transcription factors.

Viral gene carriers are being widely used as gene transfer systems in (trans)differentiation and reprogramming strategies. Forced expression of key regulators of pancreatic differentiation in stem cells, liver cells, pancreatic duct cells, or cells from the exocrine pancreas, can lead to the initiat...

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Main Authors: Arnaud Zaldumbide, Françoise Carlotti, Manuel A Gonçalves, Shoshan Knaän-Shanzer, Steve J Cramer, Bart O Roep, Emmanuel J H J Wiertz, Rob C Hoeben
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23110179/?tool=EBI
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author Arnaud Zaldumbide
Françoise Carlotti
Manuel A Gonçalves
Shoshan Knaän-Shanzer
Steve J Cramer
Bart O Roep
Emmanuel J H J Wiertz
Rob C Hoeben
author_facet Arnaud Zaldumbide
Françoise Carlotti
Manuel A Gonçalves
Shoshan Knaän-Shanzer
Steve J Cramer
Bart O Roep
Emmanuel J H J Wiertz
Rob C Hoeben
author_sort Arnaud Zaldumbide
collection DOAJ
description Viral gene carriers are being widely used as gene transfer systems in (trans)differentiation and reprogramming strategies. Forced expression of key regulators of pancreatic differentiation in stem cells, liver cells, pancreatic duct cells, or cells from the exocrine pancreas, can lead to the initiation of endocrine pancreatic differentiation. While several viral vector systems have been employed in such studies, the results reported with adenovirus vectors have been the most promising in vitro and in vivo. In this study, we examined whether the viral vector system itself could impact the differentiation capacity of human bone-marrow derived mesenchymal stem cells (hMSCs) toward the endocrine lineage. Lentivirus-mediated expression of Pdx-1, Ngn-3, and Maf-A alone or in combination does not lead to robust expression of any of the endocrine hormones (i.e. insulin, glucagon and somatostatin) in hMSCs. Remarkably, subsequent transduction of these genetically modified cells with an irrelevant early region 1 (E1)-deleted adenoviral vector potentiates the differentiation stimulus and promotes glucagon gene expression in hMSCs by affecting the chromatin structure. This adenovirus stimulation was observed upon infection with an E1-deleted adenovirus vector, but not after exposure to helper-dependent adenovirus vectors, pointing at the involvement of genes retained in the E1-deleted adenovirus vector in this phenomenon. Lentivirus mediated expression of the adenovirus E4-ORF3 mimics the adenovirus effect. From these data we conclude that E1-deleted adenoviral vectors are not inert gene-transfer vectors and contribute to the modulation of the cellular differentiation pathways.
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spelling doaj.art-457a7c07e9944d708545135dd0ecfe6e2022-12-21T23:08:43ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01710e4809310.1371/journal.pone.0048093Adenoviral vectors stimulate glucagon transcription in human mesenchymal stem cells expressing pancreatic transcription factors.Arnaud ZaldumbideFrançoise CarlottiManuel A GonçalvesShoshan Knaän-ShanzerSteve J CramerBart O RoepEmmanuel J H J WiertzRob C HoebenViral gene carriers are being widely used as gene transfer systems in (trans)differentiation and reprogramming strategies. Forced expression of key regulators of pancreatic differentiation in stem cells, liver cells, pancreatic duct cells, or cells from the exocrine pancreas, can lead to the initiation of endocrine pancreatic differentiation. While several viral vector systems have been employed in such studies, the results reported with adenovirus vectors have been the most promising in vitro and in vivo. In this study, we examined whether the viral vector system itself could impact the differentiation capacity of human bone-marrow derived mesenchymal stem cells (hMSCs) toward the endocrine lineage. Lentivirus-mediated expression of Pdx-1, Ngn-3, and Maf-A alone or in combination does not lead to robust expression of any of the endocrine hormones (i.e. insulin, glucagon and somatostatin) in hMSCs. Remarkably, subsequent transduction of these genetically modified cells with an irrelevant early region 1 (E1)-deleted adenoviral vector potentiates the differentiation stimulus and promotes glucagon gene expression in hMSCs by affecting the chromatin structure. This adenovirus stimulation was observed upon infection with an E1-deleted adenovirus vector, but not after exposure to helper-dependent adenovirus vectors, pointing at the involvement of genes retained in the E1-deleted adenovirus vector in this phenomenon. Lentivirus mediated expression of the adenovirus E4-ORF3 mimics the adenovirus effect. From these data we conclude that E1-deleted adenoviral vectors are not inert gene-transfer vectors and contribute to the modulation of the cellular differentiation pathways.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23110179/?tool=EBI
spellingShingle Arnaud Zaldumbide
Françoise Carlotti
Manuel A Gonçalves
Shoshan Knaän-Shanzer
Steve J Cramer
Bart O Roep
Emmanuel J H J Wiertz
Rob C Hoeben
Adenoviral vectors stimulate glucagon transcription in human mesenchymal stem cells expressing pancreatic transcription factors.
PLoS ONE
title Adenoviral vectors stimulate glucagon transcription in human mesenchymal stem cells expressing pancreatic transcription factors.
title_full Adenoviral vectors stimulate glucagon transcription in human mesenchymal stem cells expressing pancreatic transcription factors.
title_fullStr Adenoviral vectors stimulate glucagon transcription in human mesenchymal stem cells expressing pancreatic transcription factors.
title_full_unstemmed Adenoviral vectors stimulate glucagon transcription in human mesenchymal stem cells expressing pancreatic transcription factors.
title_short Adenoviral vectors stimulate glucagon transcription in human mesenchymal stem cells expressing pancreatic transcription factors.
title_sort adenoviral vectors stimulate glucagon transcription in human mesenchymal stem cells expressing pancreatic transcription factors
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23110179/?tool=EBI
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