Zed by boiling in 35 ml 2X LDS buffer (Invitrogen) [13]. Equal amounts

Zed by boiling in 35 ml 2X LDS buffer (Invitrogen) [13]. Equal amounts of protein (20?0 mg) were separated by gel electrophoresis using NuPAGE Novex 4?2 Bis-Tris gel in MOPS buffer and transferred using the iBlot Blotting System with nitrocellulose membranes (Invitrogen). Blots were probed with antibodies against human alpha-globin (Santa Cruz Biotechnology, Santa Cruz, CA), beta-globin (Abnova, Walnut, CA), gammaglobin (Abnova), and the appropriate horseradish peroxidaseconjugated secondary antibodies (Santa Cruz Biotechnology). Immunoreactive proteins were detected and visualized using ECL Plus Western detection reagents (GE Healthcare, Pascataway, NJ). Soluble fractions were probed for beta-actin (Abcam, Cambridge, MA) antibody, and insoluble fractions were probed for glycophorin A (Santa Cruz biotechnology) as loading controls. Band intensities were analyzed using the Image J software program (http://rsbweb.nih.gov/ij/).Lentiviral shRNA TransductionClone TRCN0000232626 59-CCGGCTTGGACCCAGAGGTTCTTTGCTCGAGCAAAGAACCTCTGGGTCCAAGTTTTTG-39 (Sigma Aldrich) targeting human beta-globin mRNA was used. Non-targeting shRNA control SHC002V (Sigma Aldrich) served as donor-matched controls. Cryopreserved CD34+ cells were washed and placed in phase I culture medium at an initial concentration of 250,000 cells/ml. After three days, 300,000 cells were transduced in 300 ml of phase I culture medium containing the viral particles (multiplicity of infection of 12). After 24 hours, the cells were resuspended in 4.0 ml phase I culture medium containing 0.5 mg/ml HDAC-IN-3 chemical information puromycin for an additional three days prior to pelleting and resuspension in 15 ml of phase II culture medium. The phase II culture medium was not supplemented with puromycin, since puromycin selection of mock-transduced cells resulted in complete cell death under these conditions.ELISA AnalysisQuantification of GDF15 was performed on serum from culture day 21 cells using the DuoSet ELISA for human GDF15 (R D Systems) following the manufacturer’s protocol [14]. The optical density was read utilizing the ELx808 Absorbance Microplate Reader (BioTek, Winooski, VT).Statistical AnalysisReplicate data are expressed as means 6 standard deviation (SD) with significance calculated by Student’s t test.A Synthetic Model of Beta-ThalassemiaResults Globin mRNA Expression PatternHuman CD34+ cells from healthy volunteers were cultured ex vivo for 21 days in a two-phase, serum free system to engineer a beta-thalassemia major model. shRNA technology was employed to target silencing of human beta-globin mRNA expression. Informatics analyses of the TRCN0000232626 clone sequence revealed reduced levels of both beta- and delta-globin mRNA. Globin mRNA expression profiles were measured in three separate donors on culture day 14 by QPCR as previously described [11]. Figure 1A shows that greater than 90 of betaglobin mRNA was silenced when compared to the control (nontargeting shRNA, SHC002V) (control = 4.0610761.46106 copies/ng cDNA vs. beta-KD = 2.5610661.66106 copies/ng cDNA, p = 0.01). The gamma-globin mRNA demonstrated a less than 2 fold increase in beta-KD when compared to control (control = 1.7610661.26106 copies/ng cDNA vs. betaKD = 3.4610661.46106 copies/ng cDNA). Delta-globin mRNA showed a 4.5 fold decrease in beta-KD compared to the control (control = 6.9610568.36104 copies/ng cDNA vs. betaKD = 1.5610562.36104 copies/ng cDNA). There was an insignificant increase in the expression of epsilon-globin mRNA. Alph.Zed by boiling in 35 ml 2X LDS buffer (Invitrogen) [13]. Equal amounts of protein (20?0 mg) were separated by gel electrophoresis using NuPAGE Novex 4?2 Bis-Tris gel in MOPS buffer and transferred using the iBlot Blotting System with nitrocellulose membranes (Invitrogen). Blots were probed with antibodies against human alpha-globin (Santa Cruz Biotechnology, Santa Cruz, CA), beta-globin (Abnova, Walnut, CA), gammaglobin (Abnova), and the appropriate horseradish peroxidaseconjugated secondary antibodies (Santa Cruz Biotechnology). Immunoreactive proteins were detected and visualized using ECL Plus Western detection reagents (GE Healthcare, Pascataway, NJ). Soluble fractions were probed for beta-actin (Abcam, Cambridge, MA) antibody, and insoluble fractions were probed for glycophorin A (Santa Cruz biotechnology) as loading controls. Band intensities were analyzed using the Image J software program (http://rsbweb.nih.gov/ij/).Lentiviral shRNA TransductionClone TRCN0000232626 59-CCGGCTTGGACCCAGAGGTTCTTTGCTCGAGCAAAGAACCTCTGGGTCCAAGTTTTTG-39 (Sigma Aldrich) targeting human beta-globin mRNA was used. Non-targeting shRNA control SHC002V (Sigma Aldrich) served as donor-matched controls. Cryopreserved CD34+ cells were washed and placed in phase I culture medium at an initial concentration of 250,000 cells/ml. After three days, 300,000 cells were transduced in 300 ml of phase I culture medium containing the viral particles (multiplicity of infection of 12). After 24 hours, the cells were resuspended in 4.0 ml phase I culture medium containing 0.5 mg/ml puromycin for an additional three days prior to pelleting and resuspension in 15 ml of phase II culture medium. The phase II culture medium was not supplemented with puromycin, since puromycin selection of mock-transduced cells resulted in complete cell death under these conditions.ELISA AnalysisQuantification of GDF15 was performed on serum from culture day 21 cells using the DuoSet ELISA for human GDF15 (R D Systems) following the manufacturer’s protocol [14]. The optical density was read utilizing the ELx808 Absorbance Microplate Reader (BioTek, Winooski, VT).Statistical AnalysisReplicate data are expressed as means 6 standard deviation (SD) with significance calculated by Student’s t test.A Synthetic Model of Beta-ThalassemiaResults Globin mRNA Expression PatternHuman CD34+ cells from healthy volunteers were cultured ex vivo for 21 days in a two-phase, serum free system to engineer a beta-thalassemia major model. shRNA technology was employed to target silencing of human beta-globin mRNA expression. Informatics analyses of the TRCN0000232626 clone sequence revealed reduced levels of both beta- and delta-globin mRNA. Globin mRNA expression profiles were measured in three separate donors on culture day 14 by QPCR as previously described [11]. Figure 1A shows that greater than 90 of betaglobin mRNA was silenced when compared to the control (nontargeting shRNA, SHC002V) (control = 4.0610761.46106 copies/ng cDNA vs. beta-KD = 2.5610661.66106 copies/ng cDNA, p = 0.01). The gamma-globin mRNA demonstrated a less than 2 fold increase in beta-KD when compared to control (control = 1.7610661.26106 copies/ng cDNA vs. betaKD = 3.4610661.46106 copies/ng cDNA). Delta-globin mRNA showed a 4.5 fold decrease in beta-KD compared to the control (control = 6.9610568.36104 copies/ng cDNA vs. betaKD = 1.5610562.36104 copies/ng cDNA). There was an insignificant increase in the expression of epsilon-globin mRNA. Alph.