Uyesaka N, Hasegawa S, Ishioka N, Ishioka R, Shio H, Schechter A N
Department of Physiology, Nippon Medical School, Tokyo 113, Japan.
Biorheology. 1992 Mar-Jun;29(2-3):217-29. doi: 10.3233/bir-1992-292-303.
The effect of superoxide anions (O2-) on red blood cells (RBC) deformability and membrane proteins was investigated using hypoxanthine-xanthine oxidase system. Exposure of RBC to O2- caused a marked decrease in RBC deformability with a concomitant increase in cell volume and shape changes. The RBC exposed to O2- also displayed pronounced degradation of membrane proteins such as band 3 protein and spectrin; new bands of low molecular weight products appeared as the original membrane proteins tended to diminish, without the appearance of high molecular weight products. Since the membrane proteins are involved in processes regulating membrane properties such as permeability and viscoelasticity, the decreased deformability induced by O2- may be attributable to changes in membrane proteins. Interestingly, resealed ghosts exposed to O2- did not show any significant change in membrane proteins, which suggests the existence of further generation of O2- and subsequent production of other active oxygen species mediated by O2(-)-initiated autoxidation of hemoglobin in intact RBC. Furthermore, electrophoretic analysis suggested that active oxygens increased the endogenous proteolytic susceptibility of RBC. In conclusion, a close linkage was suggested between RBC deformability and the membrane proteins.
利用次黄嘌呤 - 黄嘌呤氧化酶系统研究了超氧阴离子(O2-)对红细胞(RBC)变形性和膜蛋白的影响。将RBC暴露于O2-会导致RBC变形性显著降低,同时细胞体积增加且形状改变。暴露于O2-的RBC还表现出膜蛋白如带3蛋白和血影蛋白的明显降解;随着原始膜蛋白趋于减少,出现了低分子量产物的新条带,而未出现高分子量产物。由于膜蛋白参与调节膜特性如通透性和粘弹性的过程,O2-诱导的变形性降低可能归因于膜蛋白的变化。有趣的是,暴露于O2-的重封血影在膜蛋白上未显示任何显著变化,这表明在完整RBC中存在由O2-引发的血红蛋白自氧化进一步产生O2-以及随后产生其他活性氧物种的情况。此外,电泳分析表明活性氧增加了RBC的内源性蛋白水解敏感性。总之,提示RBC变形性与膜蛋白之间存在密切联系。