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. 2019 Sep 30;32(2):101–112. doi: 10.4103/tcmj.tcmj_147_19

Table 1.

Methods and transcription factors for the generation of induced pluripotent stem cells

Methods Factors Reference
Single lentiviral vectors expressing “stem cell cassette” with Cre-Lox transgene excision system Oct4, Klf4, Sox2, cMyc [24]
Cre-recombinase excisable DOX-inducible lentiviral vectors system Oct4, Klf4, Sox2, cMyc [25]
Repeated transfection of two expression plasmids without viral vectors system (cDNA of Oct3/4, Sox2, Klf4) and cDNA of cMyc [26]
Nonintegrating adenoviral vectors system Oct4, Sox2, Klf4, cMyc [27]
Nonintegrating Sendai virus-based vector system Oct4, Sox2, Klf4, cMyc [28]
Recombinant reprogramming proteins system (fusion of poly-arginine protein transduction domain to the C terminus of transcription factors) Oct4, Sox2, Klf4, cMyc [29]
Human artificial chromosomes (HACs) vectors (iHAC1 and iHAC2) system Oct4, Sox2, Klf4, cMyc [30]
Synthetic modified mRNA transfection system Oct4, Sox2, Klf4, cMyc [31]
Direct transfection of mature double-strand microRNAs (miRNAs) system Combination of mir-200c, mir-302 s and mir-369 s [32]
Doxycycline-inducible factors delivered by “piggyback” transposition system Oct4, Sox2, Klf4, cMyc [33]
Nonviral minicircle DNA vectors system Oct4, Sox2, Nanog, Lin28 [34]
Nonintegrating episomal plasmid vectors system Oct4, Sox2, Nanog, Lin28, Klf4, cMyc [35]