2016
The Aberrant DNA Methylation Profile of Human Induced Pluripotent Stem Cells Is Connected to the Reprogramming Process and Is Normalized During In Vitro Culture
TESAŘOVÁ, Lenka, Pavel ŠIMARA, Stanislav STEJSKAL a Irena KRONTORÁD KOUTNÁZákladní údaje
Originální název
The Aberrant DNA Methylation Profile of Human Induced Pluripotent Stem Cells Is Connected to the Reprogramming Process and Is Normalized During In Vitro Culture
Autoři
TESAŘOVÁ, Lenka (203 Česká republika, domácí), Pavel ŠIMARA (203 Česká republika, domácí), Stanislav STEJSKAL (203 Česká republika, domácí) a Irena KRONTORÁD KOUTNÁ (203 Česká republika, garant, domácí)
Vydání
PLOS ONE, Public Library of Science, 2016, 1932-6203
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10601 Cell biology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 2.806
Kód RIV
RIV/00216224:14330/16:00088006
Organizační jednotka
Fakulta informatiky
UT WoS
000378389200077
Klíčová slova anglicky
pluripotent stem cells; DNA methylation; MethylScreen technology; CpG islands; pluripotency and differentiation markers
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 8. 2. 2021 15:23, Mgr. Tereza Miškechová
Anotace
V originále
The potential clinical applications of human induced pluripotent stem cells (hiPSCs) are limited by genetic and epigenetic variations among hiPSC lines and the question of their equivalency with human embryonic stem cells (hESCs). We used MethylScreen technology to determine the DNA methylation profile of pluripotency and differentiation markers in hiPSC lines from different source cell types compared to hESCs and hiPSC source cells. After derivation, hiPSC lines compromised a heterogeneous population characterized by variable levels of aberrant DNA methylation. These aberrations were induced during somatic cell reprogramming and their levels were associated with the type of hiPSC source cells. hiPSC population heterogeneity was reduced during prolonged culture and hiPSCs acquired an hESC-like methylation profile. In contrast, the expression of differentiation marker genes in hiPSC lines remained distinguishable from that in hESCs. Taken together, in vitro culture facilitates hiPSC acquisition of hESC epigenetic characteristics. However, differences remain between both pluripotent stem cell types, which must be considered before their use in downstream applications.
Návaznosti
GBP302/12/G157, projekt VaV |
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LM2015090, projekt VaV |
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