ŠIMARA, Pavel, Lenka TESAŘOVÁ, Stanislava PAĎOUROVÁ and Irena KRONTORÁD KOUTNÁ. Generation of Human Induced Pluripotent Stem Cells Using Genome Integrating or Non-integrating Methods. Folia Biologica. Praha: Univerzita Karlova, 2014, vol. 60, S1, p. 85-89. ISSN 0015-5500.
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Basic information
Original name Generation of Human Induced Pluripotent Stem Cells Using Genome Integrating or Non-integrating Methods
Authors ŠIMARA, Pavel (203 Czech Republic, belonging to the institution), Lenka TESAŘOVÁ (203 Czech Republic, belonging to the institution), Stanislava PAĎOUROVÁ (703 Slovakia, belonging to the institution) and Irena KRONTORÁD KOUTNÁ (203 Czech Republic, guarantor, belonging to the institution).
Edition Folia Biologica, Praha, Univerzita Karlova, 2014, 0015-5500.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10601 Cell biology
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 1.000
RIV identification code RIV/00216224:14330/14:00074034
Organization unit Faculty of Informatics
UT WoS 000343275800014
Keywords (in Czech) hiPSCs; lentivirus; Sendai virus; episomalní reprogramace
Keywords in English hiPSCs; lentivirus; Sendai virus; episomal reprogramming
Tags cbia-web
Changed by Changed by: Mgr. Pavel Šimara, Ph.D., učo 67594. Changed: 2/3/2018 10:06.
Abstract
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.
Links
CZ.1.07/2.3.00/30.0030, interní kód MUName: Rozvoj lidských zdrojů pro oblast buněčné biologie
Investor: Ministry of Education, Youth and Sports of the CR, 2.3 Human resources in research and development
GBP302/12/G157, research and development projectName: Dynamika a organizace chromosomů během buněčného cyklu a při diferenciaci v normě a patologii
Investor: Czech Science Foundation
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