2014
Generation of Human Induced Pluripotent Stem Cells Using Genome Integrating or Non-integrating Methods
ŠIMARA, Pavel, Lenka TESAŘOVÁ, Stanislava PAĎOUROVÁ a Irena KRONTORÁD KOUTNÁZákladní údaje
Originální název
Generation of Human Induced Pluripotent Stem Cells Using Genome Integrating or Non-integrating Methods
Autoři
ŠIMARA, Pavel (203 Česká republika, domácí), Lenka TESAŘOVÁ (203 Česká republika, domácí), Stanislava PAĎOUROVÁ (703 Slovensko, domácí) a Irena KRONTORÁD KOUTNÁ (203 Česká republika, garant, domácí)
Vydání
Folia Biologica, Praha, Univerzita Karlova, 2014, 0015-5500
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10601 Cell biology
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 1.000
Kód RIV
RIV/00216224:14330/14:00074034
Organizační jednotka
Fakulta informatiky
UT WoS
000343275800014
Klíčová slova česky
hiPSCs; lentivirus; Sendai virus; episomalní reprogramace
Klíčová slova anglicky
hiPSCs; lentivirus; Sendai virus; episomal reprogramming
Štítky
Změněno: 2. 3. 2018 10:06, Mgr. Pavel Šimara, Ph.D.
Anotace
V originále
Preclinical studies have demonstrated the promising potential of human induced pluripotent stem cells (hiPSCs) for clinical application. To fulfil this goal, efficient and safe methods to generate them must be established. Various reprogramming techniques were presented during seven years of hiPSCs research. Genome non-integrating and completely xeno-free protocols from the first biopsy to stable hiPSC clones are highly preferable in terms of future clinical application. In this commentary article, we summarize the reprogramming experiments performed in our laboratories. We successfully generated hiPSCs using STEMCCA lentivirus, Sendai virus or episomal vectors. Human neonatal fibroblasts and CD34+ blood progenitors were used as cell sources and were maintained either on mouse embryonic feeder cells or in feeder-free conditions. The reprogramming efficiency was comparable for all three methods and both cell types, while the best results were obtained in feeder-free conditions.
Návaznosti
CZ.1.07/2.3.00/30.0030, interní kód MU |
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GBP302/12/G157, projekt VaV |
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