Erythrocyte membrane protein abnormalities in beta-thalassemia of the Li nationality in Hainan.
OBJECTIVE: To determine the composition of abnormal red cell membrane skeleton. METHODS: By sodium dodecyl sulphate polyacrylamide gel electrophoresis of ghostcorpuscles, we quantified the amount of protein by densitometric evaluation. RESULTS: The results showed that in beta-thalassemia, the amount of spectrin, 4.5 protein and globin significantly increased compared with the controls (26.05 +/- 1.46, 21.69 +/- 1.86; 22.87 +/- 5.61, 12.99 +/- 2.33; 15.23 +/- 3.31 and 4.97 +/- 2.73, respectively, P < 0.05). CONCLUSION: These data suggest that the erythrocyte membrane protein composition matched with globin in patients with beta-thalassemia of the racial Li minority are different from the normal control. These factors increase rigidity but decrease deformability of the beta-thalassemic red cell membrane, which may lead to hemolytic anemia.