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A New FACS Approach Isolates hESC Derived Endoderm Using Transcription Factors

We show that high quality microarray gene expression profiles can be obtained following FACS sorting of cells using combinations of transcription factors. We use this transcription factor FACS (tfFACS) methodology to perform a genomic analysis of hESC-derived endodermal lineages marked by combinatio...

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Detalles Bibliográficos
Autores principales: Pan, Yuqiong, Ouyang, Zhengqing, Wong, Wing Hung, Baker, Julie C.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052315/
https://www.ncbi.nlm.nih.gov/pubmed/21408072
http://dx.doi.org/10.1371/journal.pone.0017536
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author Pan, Yuqiong
Ouyang, Zhengqing
Wong, Wing Hung
Baker, Julie C.
author_facet Pan, Yuqiong
Ouyang, Zhengqing
Wong, Wing Hung
Baker, Julie C.
author_sort Pan, Yuqiong
collection PubMed
description We show that high quality microarray gene expression profiles can be obtained following FACS sorting of cells using combinations of transcription factors. We use this transcription factor FACS (tfFACS) methodology to perform a genomic analysis of hESC-derived endodermal lineages marked by combinations of SOX17, GATA4, and CXCR4, and find that triple positive cells have a much stronger definitive endoderm signature than other combinations of these markers. Additionally, SOX17(+) GATA4(+) cells can be obtained at a much earlier stage of differentiation, prior to expression of CXCR4(+) cells, providing an important new tool to isolate this earlier definitive endoderm subtype. Overall, tfFACS represents an advancement in FACS technology which broadly crosses multiple disciplines, most notably in regenerative medicine to redefine cellular populations.
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spelling pubmed-30523152011-03-15 A New FACS Approach Isolates hESC Derived Endoderm Using Transcription Factors Pan, Yuqiong Ouyang, Zhengqing Wong, Wing Hung Baker, Julie C. PLoS One Research Article We show that high quality microarray gene expression profiles can be obtained following FACS sorting of cells using combinations of transcription factors. We use this transcription factor FACS (tfFACS) methodology to perform a genomic analysis of hESC-derived endodermal lineages marked by combinations of SOX17, GATA4, and CXCR4, and find that triple positive cells have a much stronger definitive endoderm signature than other combinations of these markers. Additionally, SOX17(+) GATA4(+) cells can be obtained at a much earlier stage of differentiation, prior to expression of CXCR4(+) cells, providing an important new tool to isolate this earlier definitive endoderm subtype. Overall, tfFACS represents an advancement in FACS technology which broadly crosses multiple disciplines, most notably in regenerative medicine to redefine cellular populations. Public Library of Science 2011-03-09 /pmc/articles/PMC3052315/ /pubmed/21408072 http://dx.doi.org/10.1371/journal.pone.0017536 Text en Pan et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pan, Yuqiong
Ouyang, Zhengqing
Wong, Wing Hung
Baker, Julie C.
A New FACS Approach Isolates hESC Derived Endoderm Using Transcription Factors
title A New FACS Approach Isolates hESC Derived Endoderm Using Transcription Factors
title_full A New FACS Approach Isolates hESC Derived Endoderm Using Transcription Factors
title_fullStr A New FACS Approach Isolates hESC Derived Endoderm Using Transcription Factors
title_full_unstemmed A New FACS Approach Isolates hESC Derived Endoderm Using Transcription Factors
title_short A New FACS Approach Isolates hESC Derived Endoderm Using Transcription Factors
title_sort new facs approach isolates hesc derived endoderm using transcription factors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052315/
https://www.ncbi.nlm.nih.gov/pubmed/21408072
http://dx.doi.org/10.1371/journal.pone.0017536
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