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Free access | 10.1172/JCI109461
Department of Radiology, Medical University of South Carolina, Charleston, South Carolina 29403
Department of Biochemistry, Medical University of South Carolina, Charleston, South Carolina 29403
Department of Pathology, Medical University of South Carolina, Charleston, South Carolina 29403
Department of Medicine, Medical University of South Carolina, Charleston, South Carolina 29403
Find articles by Spicer, K. in: JCI | PubMed | Google Scholar
Department of Radiology, Medical University of South Carolina, Charleston, South Carolina 29403
Department of Biochemistry, Medical University of South Carolina, Charleston, South Carolina 29403
Department of Pathology, Medical University of South Carolina, Charleston, South Carolina 29403
Department of Medicine, Medical University of South Carolina, Charleston, South Carolina 29403
Find articles by Allen, R. in: JCI | PubMed | Google Scholar
Department of Radiology, Medical University of South Carolina, Charleston, South Carolina 29403
Department of Biochemistry, Medical University of South Carolina, Charleston, South Carolina 29403
Department of Pathology, Medical University of South Carolina, Charleston, South Carolina 29403
Department of Medicine, Medical University of South Carolina, Charleston, South Carolina 29403
Find articles by Hallett, D. in: JCI | PubMed | Google Scholar
Department of Radiology, Medical University of South Carolina, Charleston, South Carolina 29403
Department of Biochemistry, Medical University of South Carolina, Charleston, South Carolina 29403
Department of Pathology, Medical University of South Carolina, Charleston, South Carolina 29403
Department of Medicine, Medical University of South Carolina, Charleston, South Carolina 29403
Find articles by Buse, M. in: JCI | PubMed | Google Scholar
Published July 1, 1979 - More info
Factors that influence hemoglobin (Hb)AIc synthesis by intact erythrocytes were studied in vitro. After incubation cells were lysed, and hemoglobins were separated by isoelectric focusing on polyacrylamide slab gels and quantitated by microdensitometry. HbAIc increased with time, glucose concentrations (5-500 mM), and incubation temperature (4°-37°C). Low temperatures allowed prolonged incubations with minimal hemolysis. At 4°C HbAIc increased linearly with time for 6 wk; after incubation at the highest glucose concentration, HbAIc comprised 50% of total hemoglobin.
Insulin (1 and 0.1 mU/ml) did not affect HbAIc synthesis in vitro. In addition to glucose, galactose and mannose, but not fructose, served as precursors to HbAIc. A good substrate for hexokinase (2-deoxyglucose) and a poor hexokinase substrate (3-O-methylglucose), were better precursors for HbAIc synthesis than glucose, suggesting that enzymatic phosphorylation of glucose is not required for HbAIc synthesis. Autoradiography after erythrocyte incubation with 32P-phosphate showed incorporation of radioactivity into HbAIa1 and AIa2, but not HbAIb, AIc, or A. Acetylated HbA, generated during incubation with acetylsalicylate, migrated anodal to HbAIc and clearly separated from it.
Erythrocytes from patients with insulinopenic diabetes mellitus synthesized HbAIc at the same rate as controls when incubated with identical glucose concentrations. Likewise, the rate of HbAIc synthesis by erythrocytes from patients with cystic fibrosis and congenital spherocytosis paralleled controls. When erythrocytes from cord blood and from HbC and sickle cell anemia patients were incubated with elevated concentrations of glucose, fetal Hb, HbC, and sickle Hb decreased, whereas hemoglobins focusing at isoelectric points near those expected for the corresponding glycosylated derivatives appeared in proportionately increased amounts.
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