Butterfield D A, Purdy M J, Markesbery W R
Biochim Biophys Acta. 1979 Mar 8;551(2):452-8. doi: 10.1016/0005-2736(89)90020-5.
Electron spin resonance, hematologic, and deformability studies of erythrocytes from patients with Huntington's disease have been performed A decreased deformability of Huntington's disease erythrocytes compared to normal controls was demonstrated. No difference in erythrocyte hematologic indices, osmotic fragility, reticulocyte counts, or intracellular Na+ concentration was found. Huntington's disease serum had no demonstrable effect on electron spin resonance parameters of a protein-specific spin label attached to membrane proteins in control erythrocytes compared to the effect of control serum. This finding suggests that under the conditions employed no serum component or circulating factor is responsible for the changes in the physical state of membrane proteins in Huntington's disease erythrocytes (Butterfield, D.A., Oeswein, J.Q. and Markesbery, W.R. (1977) Nature 267, 453--455). No alteration in lipid fluidity of Huntington's disease erythrocyte membranes could be discerned suggesting that the underlying molecular defect in Huntington's disease involves a membrane protein. The results of the present studies on erythrocytes strongly support the concept that Huntington's disease is associated with a generalized membrane abnormality.
对亨廷顿舞蹈症患者的红细胞进行了电子自旋共振、血液学及变形性研究。结果表明,与正常对照组相比,亨廷顿舞蹈症患者红细胞的变形性降低。在红细胞血液学指标、渗透脆性、网织红细胞计数或细胞内钠离子浓度方面未发现差异。与对照血清的作用相比,亨廷顿舞蹈症血清对附着于对照红细胞膜蛋白上的蛋白质特异性自旋标记的电子自旋共振参数没有明显影响。这一发现表明,在所采用的条件下,没有血清成分或循环因子导致亨廷顿舞蹈症患者红细胞膜蛋白物理状态的改变(巴特菲尔德,D.A.,奥施温,J.Q.和马克斯贝里,W.R.(1977年)《自然》267卷,453 - 455页)。未发现亨廷顿舞蹈症患者红细胞膜脂质流动性有改变,这表明亨廷顿舞蹈症潜在的分子缺陷涉及膜蛋白。目前对红细胞的研究结果有力地支持了亨廷顿舞蹈症与普遍存在的膜异常有关这一概念。