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Cell-Penetrating Peptide as a Means of Directing the Differentiation of Induced Pluripotent Stem Cells

Protein transduction using cell-penetrating peptides (CPPs) is useful for the delivery of large protein molecules, including some transcription factors. This method is safer than gene transfection methods with a viral vector because there is no risk of genomic integration of the exogenous DNA. Recen...

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Detalles Bibliográficos
Autores principales: Kaitsuka, Taku, Tomizawa, Kazuhito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661845/
https://www.ncbi.nlm.nih.gov/pubmed/26561805
http://dx.doi.org/10.3390/ijms161125986
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author Kaitsuka, Taku
Tomizawa, Kazuhito
author_facet Kaitsuka, Taku
Tomizawa, Kazuhito
author_sort Kaitsuka, Taku
collection PubMed
description Protein transduction using cell-penetrating peptides (CPPs) is useful for the delivery of large protein molecules, including some transcription factors. This method is safer than gene transfection methods with a viral vector because there is no risk of genomic integration of the exogenous DNA. Recently, this method was reported as a means for the induction of induced pluripotent stem (iPS) cells, directing the differentiation into specific cell types and supporting gene editing/correction. Furthermore, we developed a direct differentiation method to obtain a pancreatic lineage from mouse and human pluripotent stem cells via the protein transduction of three transcription factors, Pdx1, NeuroD, and MafA. Here, we discuss the possibility of using CPPs as a means of directing the differentiation of iPS cells and other stem cell technologies.
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spelling pubmed-46618452015-12-10 Cell-Penetrating Peptide as a Means of Directing the Differentiation of Induced Pluripotent Stem Cells Kaitsuka, Taku Tomizawa, Kazuhito Int J Mol Sci Review Protein transduction using cell-penetrating peptides (CPPs) is useful for the delivery of large protein molecules, including some transcription factors. This method is safer than gene transfection methods with a viral vector because there is no risk of genomic integration of the exogenous DNA. Recently, this method was reported as a means for the induction of induced pluripotent stem (iPS) cells, directing the differentiation into specific cell types and supporting gene editing/correction. Furthermore, we developed a direct differentiation method to obtain a pancreatic lineage from mouse and human pluripotent stem cells via the protein transduction of three transcription factors, Pdx1, NeuroD, and MafA. Here, we discuss the possibility of using CPPs as a means of directing the differentiation of iPS cells and other stem cell technologies. MDPI 2015-11-06 /pmc/articles/PMC4661845/ /pubmed/26561805 http://dx.doi.org/10.3390/ijms161125986 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Kaitsuka, Taku
Tomizawa, Kazuhito
Cell-Penetrating Peptide as a Means of Directing the Differentiation of Induced Pluripotent Stem Cells
title Cell-Penetrating Peptide as a Means of Directing the Differentiation of Induced Pluripotent Stem Cells
title_full Cell-Penetrating Peptide as a Means of Directing the Differentiation of Induced Pluripotent Stem Cells
title_fullStr Cell-Penetrating Peptide as a Means of Directing the Differentiation of Induced Pluripotent Stem Cells
title_full_unstemmed Cell-Penetrating Peptide as a Means of Directing the Differentiation of Induced Pluripotent Stem Cells
title_short Cell-Penetrating Peptide as a Means of Directing the Differentiation of Induced Pluripotent Stem Cells
title_sort cell-penetrating peptide as a means of directing the differentiation of induced pluripotent stem cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661845/
https://www.ncbi.nlm.nih.gov/pubmed/26561805
http://dx.doi.org/10.3390/ijms161125986
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