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Hemoglobin F (HbF) is an X chromosome gene product that is present in about 8.5% of African-Americans but at a high concentration (greater than 50%) only in a small percentage of hemoglobin S (HbS) beta thalassemia heterozygotes. Therefore, a practical use of HbF as a drug is not possible. To study its effect on the properties of HbF, we transfused HeLa cells to rats bearing a high concentration of HbF (5.3 g/dl) and obtained HbF-rich hemolysates. Hemoglobin (Hb) analysis showed that the percentage of HbF increased to 21.4 +/- 1.9% in the HeLa-hemolysate-transfused group. The amount of globin mRNA decreased by 22% compared to the HbF-depleted control (disease) group. The presence of HeLa cell Hb in the transfused hemolysate was confirmed by the coprecipitation of Hb with HeLa cell membrane, by the analysis of globin gene expression, and by the (125)I-surface labelling of the cells. This association of HeLa cell Hb with high HbF was found to alter the properties of HbF. The stability of HbF in the Hemolysate group was increased about 10% compared to the disease group. In addition, the association of HeLa cell Hb decreased the lability of HbF. The globin mixture containing 20% HbF was prepared by
