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CXCL4/PF4 is a predictive biomarker of cardiac differentiation potential of human induced pluripotent stem cells

Selection of human induced pluripotent stem cell (hiPSC) lines with high cardiac differentiation potential is important for regenerative therapy and drug screening. We aimed to identify biomarkers for predicting cardiac differentiation potential of hiPSC lines by comparing the gene expression profil...

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Autores principales: Ohashi, Fumiya, Miyagawa, Shigeru, Yasuda, Satoshi, Miura, Takumi, Kuroda, Takuya, Itoh, Masayoshi, Kawaji, Hideya, Ito, Emiko, Yoshida, Shohei, Saito, Atsuhiro, Sameshima, Tadashi, Kawai, Jun, Sawa, Yoshiki, Sato, Yoji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420577/
https://www.ncbi.nlm.nih.gov/pubmed/30874579
http://dx.doi.org/10.1038/s41598-019-40915-w
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author Ohashi, Fumiya
Miyagawa, Shigeru
Yasuda, Satoshi
Miura, Takumi
Kuroda, Takuya
Itoh, Masayoshi
Kawaji, Hideya
Ito, Emiko
Yoshida, Shohei
Saito, Atsuhiro
Sameshima, Tadashi
Kawai, Jun
Sawa, Yoshiki
Sato, Yoji
author_facet Ohashi, Fumiya
Miyagawa, Shigeru
Yasuda, Satoshi
Miura, Takumi
Kuroda, Takuya
Itoh, Masayoshi
Kawaji, Hideya
Ito, Emiko
Yoshida, Shohei
Saito, Atsuhiro
Sameshima, Tadashi
Kawai, Jun
Sawa, Yoshiki
Sato, Yoji
author_sort Ohashi, Fumiya
collection PubMed
description Selection of human induced pluripotent stem cell (hiPSC) lines with high cardiac differentiation potential is important for regenerative therapy and drug screening. We aimed to identify biomarkers for predicting cardiac differentiation potential of hiPSC lines by comparing the gene expression profiles of six undifferentiated hiPSC lines with different cardiac differentiation capabilities. We used three platforms of gene expression analysis, namely, cap analysis of gene expression (CAGE), mRNA array, and microRNA array to efficiently screen biomarkers related to cardiac differentiation of hiPSCs. Statistical analysis revealed candidate biomarker genes with significant correlation between the gene expression levels in the undifferentiated hiPSCs and their cardiac differentiation potential. Of the candidate genes, PF4 was validated as a biomarker expressed in undifferentiated hiPSCs with high potential for cardiac differentiation in 13 additional hiPSC lines. Our observations suggest that PF4 may be a useful biomarker for selecting hiPSC lines appropriate for the generation of cardiomyocytes.
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spelling pubmed-64205772019-03-19 CXCL4/PF4 is a predictive biomarker of cardiac differentiation potential of human induced pluripotent stem cells Ohashi, Fumiya Miyagawa, Shigeru Yasuda, Satoshi Miura, Takumi Kuroda, Takuya Itoh, Masayoshi Kawaji, Hideya Ito, Emiko Yoshida, Shohei Saito, Atsuhiro Sameshima, Tadashi Kawai, Jun Sawa, Yoshiki Sato, Yoji Sci Rep Article Selection of human induced pluripotent stem cell (hiPSC) lines with high cardiac differentiation potential is important for regenerative therapy and drug screening. We aimed to identify biomarkers for predicting cardiac differentiation potential of hiPSC lines by comparing the gene expression profiles of six undifferentiated hiPSC lines with different cardiac differentiation capabilities. We used three platforms of gene expression analysis, namely, cap analysis of gene expression (CAGE), mRNA array, and microRNA array to efficiently screen biomarkers related to cardiac differentiation of hiPSCs. Statistical analysis revealed candidate biomarker genes with significant correlation between the gene expression levels in the undifferentiated hiPSCs and their cardiac differentiation potential. Of the candidate genes, PF4 was validated as a biomarker expressed in undifferentiated hiPSCs with high potential for cardiac differentiation in 13 additional hiPSC lines. Our observations suggest that PF4 may be a useful biomarker for selecting hiPSC lines appropriate for the generation of cardiomyocytes. Nature Publishing Group UK 2019-03-15 /pmc/articles/PMC6420577/ /pubmed/30874579 http://dx.doi.org/10.1038/s41598-019-40915-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ohashi, Fumiya
Miyagawa, Shigeru
Yasuda, Satoshi
Miura, Takumi
Kuroda, Takuya
Itoh, Masayoshi
Kawaji, Hideya
Ito, Emiko
Yoshida, Shohei
Saito, Atsuhiro
Sameshima, Tadashi
Kawai, Jun
Sawa, Yoshiki
Sato, Yoji
CXCL4/PF4 is a predictive biomarker of cardiac differentiation potential of human induced pluripotent stem cells
title CXCL4/PF4 is a predictive biomarker of cardiac differentiation potential of human induced pluripotent stem cells
title_full CXCL4/PF4 is a predictive biomarker of cardiac differentiation potential of human induced pluripotent stem cells
title_fullStr CXCL4/PF4 is a predictive biomarker of cardiac differentiation potential of human induced pluripotent stem cells
title_full_unstemmed CXCL4/PF4 is a predictive biomarker of cardiac differentiation potential of human induced pluripotent stem cells
title_short CXCL4/PF4 is a predictive biomarker of cardiac differentiation potential of human induced pluripotent stem cells
title_sort cxcl4/pf4 is a predictive biomarker of cardiac differentiation potential of human induced pluripotent stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420577/
https://www.ncbi.nlm.nih.gov/pubmed/30874579
http://dx.doi.org/10.1038/s41598-019-40915-w
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