Pancreatic transcription factors containing protein transduction domains drive mouse embryonic stem cells towards endocrine pancreas.

Protein transduction domains (PTDs), such as the HIV1-TAT peptide, have been previously used to promote the uptake of proteins into a range of cell types, including stem cells. Here we generated pancreatic transcription factors containing PTD sequences and administered these to endoderm enriched mou...

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Main Authors: Maria João Lima, Hilary M Docherty, Yuanxiao Chen, Ludovic Vallier, Kevin Docherty
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0036481&type=printable
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author Maria João Lima
Hilary M Docherty
Yuanxiao Chen
Ludovic Vallier
Kevin Docherty
author_facet Maria João Lima
Hilary M Docherty
Yuanxiao Chen
Ludovic Vallier
Kevin Docherty
author_sort Maria João Lima
collection DOAJ
description Protein transduction domains (PTDs), such as the HIV1-TAT peptide, have been previously used to promote the uptake of proteins into a range of cell types, including stem cells. Here we generated pancreatic transcription factors containing PTD sequences and administered these to endoderm enriched mouse embryonic stem (ES) cells under conditions that were designed to mimic the pattern of expression of these factors in the developing pancreas. The ES cells were first cultured as embryoid bodies and treated with Activin A and Bone morphogenetic protein 4 (BMP4) to promote formation of definitive endoderm. Cells were subsequently plated as a monolayer and treated with different combinations of the modified recombinant transcription factors Pdx1 and MafA. The results demonstrate that each transcription factor was efficiently taken up by the cells, where they were localized in the nuclei. RT-qPCR was used to measure the expression levels of pancreatic markers. After the addition of Pdx1 alone for a period of five days, followed by the combination of Pdx1 and TAT-MafA in a second phase, up-regulation of insulin 1, insulin 2, Pdx1, Glut2, Pax4 and Nkx6.1 was observed. As assessed by immunocytochemistry, double positive insulin and Pdx1 cells were detected in the differentiated cultures. Although the pattern of pancreatic markers expression in these cultures was comparable to that of a mouse transformed β-cell line (MIN-6) and human islets, the expression levels of insulin observed in the differentiated ES cell cultures were several orders of magnitude lower. This suggests that, although PTD-TFs may prove useful in studying the role of exogenous TFs in the differentiation of ES cells towards islets and other pancreatic lineages, the amount of insulin generated is well below that required for therapeutically useful cells.
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spelling doaj-art-467acde8e3374897b28f38fd247bf4282025-08-20T02:05:32ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0175e3648110.1371/journal.pone.0036481Pancreatic transcription factors containing protein transduction domains drive mouse embryonic stem cells towards endocrine pancreas.Maria João LimaHilary M DochertyYuanxiao ChenLudovic VallierKevin DochertyProtein transduction domains (PTDs), such as the HIV1-TAT peptide, have been previously used to promote the uptake of proteins into a range of cell types, including stem cells. Here we generated pancreatic transcription factors containing PTD sequences and administered these to endoderm enriched mouse embryonic stem (ES) cells under conditions that were designed to mimic the pattern of expression of these factors in the developing pancreas. The ES cells were first cultured as embryoid bodies and treated with Activin A and Bone morphogenetic protein 4 (BMP4) to promote formation of definitive endoderm. Cells were subsequently plated as a monolayer and treated with different combinations of the modified recombinant transcription factors Pdx1 and MafA. The results demonstrate that each transcription factor was efficiently taken up by the cells, where they were localized in the nuclei. RT-qPCR was used to measure the expression levels of pancreatic markers. After the addition of Pdx1 alone for a period of five days, followed by the combination of Pdx1 and TAT-MafA in a second phase, up-regulation of insulin 1, insulin 2, Pdx1, Glut2, Pax4 and Nkx6.1 was observed. As assessed by immunocytochemistry, double positive insulin and Pdx1 cells were detected in the differentiated cultures. Although the pattern of pancreatic markers expression in these cultures was comparable to that of a mouse transformed β-cell line (MIN-6) and human islets, the expression levels of insulin observed in the differentiated ES cell cultures were several orders of magnitude lower. This suggests that, although PTD-TFs may prove useful in studying the role of exogenous TFs in the differentiation of ES cells towards islets and other pancreatic lineages, the amount of insulin generated is well below that required for therapeutically useful cells.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0036481&type=printable
spellingShingle Maria João Lima
Hilary M Docherty
Yuanxiao Chen
Ludovic Vallier
Kevin Docherty
Pancreatic transcription factors containing protein transduction domains drive mouse embryonic stem cells towards endocrine pancreas.
PLoS ONE
title Pancreatic transcription factors containing protein transduction domains drive mouse embryonic stem cells towards endocrine pancreas.
title_full Pancreatic transcription factors containing protein transduction domains drive mouse embryonic stem cells towards endocrine pancreas.
title_fullStr Pancreatic transcription factors containing protein transduction domains drive mouse embryonic stem cells towards endocrine pancreas.
title_full_unstemmed Pancreatic transcription factors containing protein transduction domains drive mouse embryonic stem cells towards endocrine pancreas.
title_short Pancreatic transcription factors containing protein transduction domains drive mouse embryonic stem cells towards endocrine pancreas.
title_sort pancreatic transcription factors containing protein transduction domains drive mouse embryonic stem cells towards endocrine pancreas
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0036481&type=printable
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