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miRNome Profiling of Purified Endoderm and Mesoderm Differentiated from hESCs Reveals Functions of miR-483-3p and miR-1263 for Cell-Fate Decisions

Pluripotent stem cells hold great promise for regenerative medicine since they can differentiate into all somatic cells. MicroRNAs (miRNAs) could be important for the regulation of these cell-fate decisions. Profiling of miRNAs revealed 19 differentially expressed miRNAs in the endoderm and 29 in th...

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Autores principales: Ishikawa, Daichi, Diekmann, Ulf, Fiedler, Jan, Just, Annette, Thum, Thomas, Lenzen, Sigurd, Naujok, Ortwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688239/
https://www.ncbi.nlm.nih.gov/pubmed/29141233
http://dx.doi.org/10.1016/j.stemcr.2017.10.011
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author Ishikawa, Daichi
Diekmann, Ulf
Fiedler, Jan
Just, Annette
Thum, Thomas
Lenzen, Sigurd
Naujok, Ortwin
author_facet Ishikawa, Daichi
Diekmann, Ulf
Fiedler, Jan
Just, Annette
Thum, Thomas
Lenzen, Sigurd
Naujok, Ortwin
author_sort Ishikawa, Daichi
collection PubMed
description Pluripotent stem cells hold great promise for regenerative medicine since they can differentiate into all somatic cells. MicroRNAs (miRNAs) could be important for the regulation of these cell-fate decisions. Profiling of miRNAs revealed 19 differentially expressed miRNAs in the endoderm and 29 in the mesoderm when analyzing FACS-purified cells derived from human embryonic stem cells. The mesodermal-enriched miR-483-3p was identified as an important regulator for the generation of mesodermal PDGFRA(+) paraxial cells. Repression of its target PGAM1 significantly increased the number of PDGFRA(+) cells. Furthermore, miR-483-3p, miR-199a-3p, and miR-214-3p might also have functions for the mesodermal progenitors. The endoderm-specific miR-489-3p and miR-1263 accelerated and increased endoderm differentiation upon overexpression. KLF4 was identified as a target of miR-1263. RNAi-mediated downregulation of KLF4 partially mimicked miR-1263 overexpression. Thus, the effects of this miRNA were mediated by facilitating differentiation through destabilization of pluripotency along with other not yet defined targets.
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spelling pubmed-56882392017-12-04 miRNome Profiling of Purified Endoderm and Mesoderm Differentiated from hESCs Reveals Functions of miR-483-3p and miR-1263 for Cell-Fate Decisions Ishikawa, Daichi Diekmann, Ulf Fiedler, Jan Just, Annette Thum, Thomas Lenzen, Sigurd Naujok, Ortwin Stem Cell Reports Article Pluripotent stem cells hold great promise for regenerative medicine since they can differentiate into all somatic cells. MicroRNAs (miRNAs) could be important for the regulation of these cell-fate decisions. Profiling of miRNAs revealed 19 differentially expressed miRNAs in the endoderm and 29 in the mesoderm when analyzing FACS-purified cells derived from human embryonic stem cells. The mesodermal-enriched miR-483-3p was identified as an important regulator for the generation of mesodermal PDGFRA(+) paraxial cells. Repression of its target PGAM1 significantly increased the number of PDGFRA(+) cells. Furthermore, miR-483-3p, miR-199a-3p, and miR-214-3p might also have functions for the mesodermal progenitors. The endoderm-specific miR-489-3p and miR-1263 accelerated and increased endoderm differentiation upon overexpression. KLF4 was identified as a target of miR-1263. RNAi-mediated downregulation of KLF4 partially mimicked miR-1263 overexpression. Thus, the effects of this miRNA were mediated by facilitating differentiation through destabilization of pluripotency along with other not yet defined targets. Elsevier 2017-11-14 /pmc/articles/PMC5688239/ /pubmed/29141233 http://dx.doi.org/10.1016/j.stemcr.2017.10.011 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Ishikawa, Daichi
Diekmann, Ulf
Fiedler, Jan
Just, Annette
Thum, Thomas
Lenzen, Sigurd
Naujok, Ortwin
miRNome Profiling of Purified Endoderm and Mesoderm Differentiated from hESCs Reveals Functions of miR-483-3p and miR-1263 for Cell-Fate Decisions
title miRNome Profiling of Purified Endoderm and Mesoderm Differentiated from hESCs Reveals Functions of miR-483-3p and miR-1263 for Cell-Fate Decisions
title_full miRNome Profiling of Purified Endoderm and Mesoderm Differentiated from hESCs Reveals Functions of miR-483-3p and miR-1263 for Cell-Fate Decisions
title_fullStr miRNome Profiling of Purified Endoderm and Mesoderm Differentiated from hESCs Reveals Functions of miR-483-3p and miR-1263 for Cell-Fate Decisions
title_full_unstemmed miRNome Profiling of Purified Endoderm and Mesoderm Differentiated from hESCs Reveals Functions of miR-483-3p and miR-1263 for Cell-Fate Decisions
title_short miRNome Profiling of Purified Endoderm and Mesoderm Differentiated from hESCs Reveals Functions of miR-483-3p and miR-1263 for Cell-Fate Decisions
title_sort mirnome profiling of purified endoderm and mesoderm differentiated from hescs reveals functions of mir-483-3p and mir-1263 for cell-fate decisions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688239/
https://www.ncbi.nlm.nih.gov/pubmed/29141233
http://dx.doi.org/10.1016/j.stemcr.2017.10.011
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