Figure 1
Figure 1. Sal does not change mRNA stability, mRNA cellular localization, or total HbA to induce HbF. (A) Neither γ-globin nor β-globin relative mRNA half-life is changed in cells treated with Sal in combination with 5 μg/mL actinomycin D (Act D) versus actinomycin D alone. Expression is reported as fold change relative to the untreated control (Untx) on day 15 prior to treatment. Actinomycin D and 6 μM Sal were simultaneously applied on day 15. mRNA expression was quantified by using primers located at either the 5′ or 3′ end of each mRNA. Error bars represent ± standard error of the mean (SEM) of 3 independent experiments. (B) Sal does not change the cytoplasmic (Cyto):nuclear (Nuc) ratio of γ- or β-globin mRNA compared with the untreated control. Cells were treated with 6 μM Sal on days 15 and 18. Cytoplasmic and nuclear RNA were isolated on days 15, 18, and 20, mRNA expression for γ- and β-globin was quantified in each compartment by using primers that spanned at least 1 exon-exon junction, and the cytoplasmic mRNA:nuclear mRNA ratio was compared. Error bars represent ± SEM of 4 independent experiments. (C) Western blotting shows that short hairpin HBB (shHBB) causes 50% knockdown of β-globin protein compared with short hairpin control (shCTRL). Protein lysates were taken on days 13, 15, and 17 of differentiation after infections on days 8 and 9. glyceraldehyde-3-phosphate dehydrogenase was used as a loading control. (D) High-performance liquid chromatography (HPLC) was performed on day 20 of culture to assess the proportions of HbF, HbA, and HbA2 in shCTRL- and shHBB-infected cells. These HPLC traces from a representative experiment reveal that shHBB enhances the percentage of HbF and percentage of HbA2 compared with shCTRL. (E) β-globin knockdown does not increase total HbF, but it does enhance total HbA2. After analysis by HPLC, the area under the curve for HbF, HbA, and HbA2 was corrected for the total Hb concentration in 2 × 106 cells. Total amounts of HbF, HbA, and HbA2 are depicted as fold change relative to the shCTRL. Error bars represent ± SEM of 3 independent experiments. P values were determined by using an unpaired 2-tailed Student t test. NS, not significant. *P < .05; **P < .001.

Sal does not change mRNA stability, mRNA cellular localization, or total HbA to induce HbF. (A) Neither γ-globin nor β-globin relative mRNA half-life is changed in cells treated with Sal in combination with 5 μg/mL actinomycin D (Act D) versus actinomycin D alone. Expression is reported as fold change relative to the untreated control (Untx) on day 15 prior to treatment. Actinomycin D and 6 μM Sal were simultaneously applied on day 15. mRNA expression was quantified by using primers located at either the 5′ or 3′ end of each mRNA. Error bars represent ± standard error of the mean (SEM) of 3 independent experiments. (B) Sal does not change the cytoplasmic (Cyto):nuclear (Nuc) ratio of γ- or β-globin mRNA compared with the untreated control. Cells were treated with 6 μM Sal on days 15 and 18. Cytoplasmic and nuclear RNA were isolated on days 15, 18, and 20, mRNA expression for γ- and β-globin was quantified in each compartment by using primers that spanned at least 1 exon-exon junction, and the cytoplasmic mRNA:nuclear mRNA ratio was compared. Error bars represent ± SEM of 4 independent experiments. (C) Western blotting shows that short hairpin HBB (shHBB) causes 50% knockdown of β-globin protein compared with short hairpin control (shCTRL). Protein lysates were taken on days 13, 15, and 17 of differentiation after infections on days 8 and 9. glyceraldehyde-3-phosphate dehydrogenase was used as a loading control. (D) High-performance liquid chromatography (HPLC) was performed on day 20 of culture to assess the proportions of HbF, HbA, and HbA2 in shCTRL- and shHBB-infected cells. These HPLC traces from a representative experiment reveal that shHBB enhances the percentage of HbF and percentage of HbA2 compared with shCTRL. (E) β-globin knockdown does not increase total HbF, but it does enhance total HbA2. After analysis by HPLC, the area under the curve for HbF, HbA, and HbA2 was corrected for the total Hb concentration in 2 × 106 cells. Total amounts of HbF, HbA, and HbA2 are depicted as fold change relative to the shCTRL. Error bars represent ± SEM of 3 independent experiments. P values were determined by using an unpaired 2-tailed Student t test. NS, not significant. *P < .05; **P < .001.

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