Production of embryonic and fetal-like red blood cells from human induced pluripotent stem cells.

We have previously shown that human embryonic stem cells can be differentiated into embryonic and fetal type of red blood cells that sequentially express three types of hemoglobins recapitulating early human erythropoiesis. We report here that we have produced iPS from three somatic cell types: adul...

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Main Authors: Chan-Jung Chang, Koyel Mitra, Mariko Koya, Michelle Velho, Romain Desprat, Jack Lenz, Eric E Bouhassira
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3192723?pdf=render
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spelling doaj-17cc7a1fc7a74f80afaee1a2c47064322020-11-25T01:46:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01610e2576110.1371/journal.pone.0025761Production of embryonic and fetal-like red blood cells from human induced pluripotent stem cells.Chan-Jung ChangKoyel MitraMariko KoyaMichelle VelhoRomain DespratJack LenzEric E BouhassiraWe have previously shown that human embryonic stem cells can be differentiated into embryonic and fetal type of red blood cells that sequentially express three types of hemoglobins recapitulating early human erythropoiesis. We report here that we have produced iPS from three somatic cell types: adult skin fibroblasts as well as embryonic and fetal mesenchymal stem cells. We show that regardless of the age of the donor cells, the iPS produced are fully reprogrammed into a pluripotent state that is undistinguishable from that of hESCs by low and high-throughput expression and detailed analysis of globin expression patterns by HPLC. This suggests that reprogramming with the four original Yamanaka pluripotency factors leads to complete erasure of all functionally important epigenetic marks associated with erythroid differentiation regardless of the age or the tissue type of the donor cells, at least as detected in these assays. The ability to produce large number of erythroid cells with embryonic and fetal-like characteristics is likely to have many translational applications.http://europepmc.org/articles/PMC3192723?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Chan-Jung Chang
Koyel Mitra
Mariko Koya
Michelle Velho
Romain Desprat
Jack Lenz
Eric E Bouhassira
spellingShingle Chan-Jung Chang
Koyel Mitra
Mariko Koya
Michelle Velho
Romain Desprat
Jack Lenz
Eric E Bouhassira
Production of embryonic and fetal-like red blood cells from human induced pluripotent stem cells.
PLoS ONE
author_facet Chan-Jung Chang
Koyel Mitra
Mariko Koya
Michelle Velho
Romain Desprat
Jack Lenz
Eric E Bouhassira
author_sort Chan-Jung Chang
title Production of embryonic and fetal-like red blood cells from human induced pluripotent stem cells.
title_short Production of embryonic and fetal-like red blood cells from human induced pluripotent stem cells.
title_full Production of embryonic and fetal-like red blood cells from human induced pluripotent stem cells.
title_fullStr Production of embryonic and fetal-like red blood cells from human induced pluripotent stem cells.
title_full_unstemmed Production of embryonic and fetal-like red blood cells from human induced pluripotent stem cells.
title_sort production of embryonic and fetal-like red blood cells from human induced pluripotent stem cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description We have previously shown that human embryonic stem cells can be differentiated into embryonic and fetal type of red blood cells that sequentially express three types of hemoglobins recapitulating early human erythropoiesis. We report here that we have produced iPS from three somatic cell types: adult skin fibroblasts as well as embryonic and fetal mesenchymal stem cells. We show that regardless of the age of the donor cells, the iPS produced are fully reprogrammed into a pluripotent state that is undistinguishable from that of hESCs by low and high-throughput expression and detailed analysis of globin expression patterns by HPLC. This suggests that reprogramming with the four original Yamanaka pluripotency factors leads to complete erasure of all functionally important epigenetic marks associated with erythroid differentiation regardless of the age or the tissue type of the donor cells, at least as detected in these assays. The ability to produce large number of erythroid cells with embryonic and fetal-like characteristics is likely to have many translational applications.
url http://europepmc.org/articles/PMC3192723?pdf=render
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