Generation of iPSC line iPSC-FH2.1 in hypoxic conditions from human foreskin fibroblasts

Human foreskin fibroblasts were used to generate the iPSC line iPSC-FH2.1 using the EF1a-hSTEMCCA-loxP vector expressing OCT4, SOX2, c-MYC and KLF4, in 5% O2 culture conditions. Stemness was confirmed, as was pluripotency both in vivo and in vitro, in normoxia and hypoxia. Human Embryonic Stem Cell...

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Autores principales: Questa, M., Romorini, L., Blüguermann, C., Solari, C.M., Neiman, G., Luzzani, C., Scassa, M.T., Sevlever, G.E., Guberman, A.S., Miriuka, S.G.
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_18735061_v16_n2_p300_Questa
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spelling todo:paper_18735061_v16_n2_p300_Questa2023-10-03T16:34:01Z Generation of iPSC line iPSC-FH2.1 in hypoxic conditions from human foreskin fibroblasts Questa, M. Romorini, L. Blüguermann, C. Solari, C.M. Neiman, G. Luzzani, C. Scassa, M.T. Sevlever, G.E. Guberman, A.S. Miriuka, S.G. kruppel like factor 4 Myc protein octamer transcription factor 4 transcription factor Sox2 octamer transcription factor 4 POU5F1 protein, human transcription factor Article cell differentiation controlled study CpG island fibroblast gene expression human human cell human embryonic stem cell hypoxic cell in vitro study in vivo study nuclear reprogramming pluripotent stem cell prepuce priority journal stem cell line cell culture comparative genomic hybridization cytology DNA methylation fibroblast fluorescence microscopy genetics induced pluripotent stem cell karyotype male metabolism prepuce promoter region real time polymerase chain reaction Cell Differentiation Cells, Cultured Cellular Reprogramming Comparative Genomic Hybridization DNA Methylation Fibroblasts Foreskin Humans Induced Pluripotent Stem Cells Karyotype Male Microscopy, Fluorescence Octamer Transcription Factor-3 Promoter Regions, Genetic Real-Time Polymerase Chain Reaction Transcription Factors Human foreskin fibroblasts were used to generate the iPSC line iPSC-FH2.1 using the EF1a-hSTEMCCA-loxP vector expressing OCT4, SOX2, c-MYC and KLF4, in 5% O2 culture conditions. Stemness was confirmed, as was pluripotency both in vivo and in vitro, in normoxia and hypoxia. Human Embryonic Stem Cell (hESC) line WA-09 and reprogrammed fibroblast primary culture HFF-FM were used as controls. © 2015 The Authors. Fil:Questa, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Romorini, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Luzzani, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Scassa, M.T. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Guberman, A.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_18735061_v16_n2_p300_Questa
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic kruppel like factor 4
Myc protein
octamer transcription factor 4
transcription factor Sox2
octamer transcription factor 4
POU5F1 protein, human
transcription factor
Article
cell differentiation
controlled study
CpG island
fibroblast
gene expression
human
human cell
human embryonic stem cell
hypoxic cell
in vitro study
in vivo study
nuclear reprogramming
pluripotent stem cell
prepuce
priority journal
stem cell line
cell culture
comparative genomic hybridization
cytology
DNA methylation
fibroblast
fluorescence microscopy
genetics
induced pluripotent stem cell
karyotype
male
metabolism
prepuce
promoter region
real time polymerase chain reaction
Cell Differentiation
Cells, Cultured
Cellular Reprogramming
Comparative Genomic Hybridization
DNA Methylation
Fibroblasts
Foreskin
Humans
Induced Pluripotent Stem Cells
Karyotype
Male
Microscopy, Fluorescence
Octamer Transcription Factor-3
Promoter Regions, Genetic
Real-Time Polymerase Chain Reaction
Transcription Factors
spellingShingle kruppel like factor 4
Myc protein
octamer transcription factor 4
transcription factor Sox2
octamer transcription factor 4
POU5F1 protein, human
transcription factor
Article
cell differentiation
controlled study
CpG island
fibroblast
gene expression
human
human cell
human embryonic stem cell
hypoxic cell
in vitro study
in vivo study
nuclear reprogramming
pluripotent stem cell
prepuce
priority journal
stem cell line
cell culture
comparative genomic hybridization
cytology
DNA methylation
fibroblast
fluorescence microscopy
genetics
induced pluripotent stem cell
karyotype
male
metabolism
prepuce
promoter region
real time polymerase chain reaction
Cell Differentiation
Cells, Cultured
Cellular Reprogramming
Comparative Genomic Hybridization
DNA Methylation
Fibroblasts
Foreskin
Humans
Induced Pluripotent Stem Cells
Karyotype
Male
Microscopy, Fluorescence
Octamer Transcription Factor-3
Promoter Regions, Genetic
Real-Time Polymerase Chain Reaction
Transcription Factors
Questa, M.
Romorini, L.
Blüguermann, C.
Solari, C.M.
Neiman, G.
Luzzani, C.
Scassa, M.T.
Sevlever, G.E.
Guberman, A.S.
Miriuka, S.G.
Generation of iPSC line iPSC-FH2.1 in hypoxic conditions from human foreskin fibroblasts
topic_facet kruppel like factor 4
Myc protein
octamer transcription factor 4
transcription factor Sox2
octamer transcription factor 4
POU5F1 protein, human
transcription factor
Article
cell differentiation
controlled study
CpG island
fibroblast
gene expression
human
human cell
human embryonic stem cell
hypoxic cell
in vitro study
in vivo study
nuclear reprogramming
pluripotent stem cell
prepuce
priority journal
stem cell line
cell culture
comparative genomic hybridization
cytology
DNA methylation
fibroblast
fluorescence microscopy
genetics
induced pluripotent stem cell
karyotype
male
metabolism
prepuce
promoter region
real time polymerase chain reaction
Cell Differentiation
Cells, Cultured
Cellular Reprogramming
Comparative Genomic Hybridization
DNA Methylation
Fibroblasts
Foreskin
Humans
Induced Pluripotent Stem Cells
Karyotype
Male
Microscopy, Fluorescence
Octamer Transcription Factor-3
Promoter Regions, Genetic
Real-Time Polymerase Chain Reaction
Transcription Factors
description Human foreskin fibroblasts were used to generate the iPSC line iPSC-FH2.1 using the EF1a-hSTEMCCA-loxP vector expressing OCT4, SOX2, c-MYC and KLF4, in 5% O2 culture conditions. Stemness was confirmed, as was pluripotency both in vivo and in vitro, in normoxia and hypoxia. Human Embryonic Stem Cell (hESC) line WA-09 and reprogrammed fibroblast primary culture HFF-FM were used as controls. © 2015 The Authors.
format JOUR
author Questa, M.
Romorini, L.
Blüguermann, C.
Solari, C.M.
Neiman, G.
Luzzani, C.
Scassa, M.T.
Sevlever, G.E.
Guberman, A.S.
Miriuka, S.G.
author_facet Questa, M.
Romorini, L.
Blüguermann, C.
Solari, C.M.
Neiman, G.
Luzzani, C.
Scassa, M.T.
Sevlever, G.E.
Guberman, A.S.
Miriuka, S.G.
author_sort Questa, M.
title Generation of iPSC line iPSC-FH2.1 in hypoxic conditions from human foreskin fibroblasts
title_short Generation of iPSC line iPSC-FH2.1 in hypoxic conditions from human foreskin fibroblasts
title_full Generation of iPSC line iPSC-FH2.1 in hypoxic conditions from human foreskin fibroblasts
title_fullStr Generation of iPSC line iPSC-FH2.1 in hypoxic conditions from human foreskin fibroblasts
title_full_unstemmed Generation of iPSC line iPSC-FH2.1 in hypoxic conditions from human foreskin fibroblasts
title_sort generation of ipsc line ipsc-fh2.1 in hypoxic conditions from human foreskin fibroblasts
url http://hdl.handle.net/20.500.12110/paper_18735061_v16_n2_p300_Questa
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