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. 2016 Sep 15;25(18):1366–1375. doi: 10.1089/scd.2016.0156

FIG. 1.

FIG. 1.

Reprogramming HFFs using synthetic modified mRNA. (A) Synthetic modified mRNAs are translated into proteins. Cells transfected with mRNA cocktail expressing reprogramming factors Klf4, cMyc, Oct4, LIN28, and Sox2. The 15-h time point was chosen for analysis as it corresponds to the average peak expression time post-transfection of the different reprogramming factors [25]. (B) More than 75% cells express reprogramming factors 15 h after mRNA transfection. The cells were fixed and immunostained for Oct4, Klf4, Sox2, c-Myc, and LIN28 15 h post-transfection with mRNA reprogramming cocktail. Nuclei were visualized with Hoechst 33342. Total cell number was calculated. Data are presented as the mean of cells positive for Oct4, Klf4, Sox2, c-Myc, and LIN28 ± standard error of the mean (n = 3). (C) Daily transfection had a deleterious effect on the cells; vast majority did not survive. Day 0: the cells before the first transfection demonstrate normal morphology and density. Day 3: decreased cell density and cell rounding indicate a high apoptotic rate. Day 6: massive apoptosis is seen. Surviving cells start undergoing mesenchymal epithelial transformation and adopt an epithelial morphology. Day 9: surviving cells continue to transition to an epithelial morphology. Day 12: first signs of compaction and colony formation are noted. Day 15: increased compaction. Cells become smaller and more hESC like. (D) Inhibitory effect of pifithrin-α on p53-mediated transcription. qPCR expression analyses of the two p53 target genes, BAX, and p21 at Day 4 of reprogramming showed decrease in BAX, but not p21 mRNA levels (n = 3 biological replicates). Transfected samples are compared with the negative control (untransfected BJ cells). Data are given by normalized mean ± standard error of the mean (n = 3); statistical significance was calculated by two-way analysis of variance with Tukey post hoc test. ****P < 0.0001. (E) An average reprogramming efficiency from two independent experiments was calculated as number of trypan blue positive colonies per total number of cells plated per well of six-well dish. HFF, human foreskin fibroblast; hESC, human embryonic stem cell; qPCR, quantitative reverse transcriptase–polymerase chain reaction.