Lessin L S, Jensen W N, Ponder E
J Exp Med. 1969 Sep 1;130(3):443-66. doi: 10.1084/jem.130.3.443.
Erythrocytes from a patient with homozygous hemoglobin C disease were subjected to gradual osmotic dehydration by incubation in hypertonic saline. Serial observations of these cells before and after 4 and 12 hr incubation were carried out by means of interference, Soret absorption, polarization microscopy, and the electron microscope employing the freeze-etching technique. Light microscopic studies showed a progressive contraction of cellular contents into central masses which, after 12 hr dehydration, formed birefringent intracellular hemoglobin crystals in 50-75% of the cells. Electron microscopic study of freeze-etched replicas of these cells at 0, 4, and 12 hr of dehydration reveals progressive aggregation, alignment, and crystallization of hemoglobin molecules. Molecular aggregation found in C-C cells prior to osmotic dehydration was not seen in normal erythrocytes. Aggregation and packing varied from cell to cell. Reticulocytes showed a loosely packed aggregate mesh-work; older cells showed variation of molecular packing, which appeared tightest in cells corresponding to microspherocytes. With further loss of intracellular water, aggregates coalesced into patterns of tighter molecular packing with small regions of alignment, and, finally, crystallization occurred. Hemoglobin molecules measuring 70 A in diameter were readily identified within the period patterns of intracellular crystals. These findings suggest that the hemoglobin C molecules within C-C erythrocytes exist in an aggregated state. As the cell ages, intracellular water is lost and intermolecular distance decreases, hemoglobin C molecules polymerize into intracellular crystals. This pathological behavior of hemoglobin C is associated with a charge alteration conferred by the substitution of beta-6-lysine for glutamic acid on the external surface in the A-helix region of the beta-chain of the molecule, possibly increasing intermolecular attraction. Molecular aggregation accounts for the increased rigidity of C-C cells which leads to accelerated membrane and water loss with resultant microspherocyte formation. The microspherocyte, with highest intracellular hemoglobin concentration, rapidly undergoes intracellular crystallization, and is sequestered and destroyed by reticuloendothelial elements.
将患有纯合血红蛋白C病患者的红细胞置于高渗盐溶液中孵育,使其逐渐发生渗透性脱水。通过干涉、索雷特吸收、偏光显微镜以及采用冷冻蚀刻技术的电子显微镜,对这些细胞在孵育4小时和12小时前后进行了系列观察。光学显微镜研究显示,细胞内容物逐渐收缩成中央团块,在脱水12小时后,50%-75%的细胞内形成了双折射的细胞内血红蛋白晶体。对这些细胞在脱水0小时、4小时和12小时时的冷冻蚀刻复制品进行电子显微镜研究,发现血红蛋白分子逐渐聚集、排列并结晶。在渗透性脱水之前,C-C细胞中发现的分子聚集在正常红细胞中未见。聚集和堆积情况因细胞而异。网织红细胞显示出松散堆积的聚集网状结构;较老的细胞显示出分子堆积的变化,在对应于小球形红细胞的细胞中看起来最紧密。随着细胞内水分的进一步流失,聚集体合并成分子堆积更紧密且有小区域排列的模式,最终发生结晶。在细胞内晶体的周期模式内很容易识别出直径为70埃的血红蛋白分子。这些发现表明,C-C红细胞内的血红蛋白C分子以聚集状态存在。随着细胞老化,细胞内水分流失,分子间距离减小,血红蛋白C分子聚合成细胞内晶体。血红蛋白C的这种病理行为与分子β链A螺旋区域外表面上β-6-赖氨酸取代谷氨酸所赋予的电荷改变有关,这可能增加了分子间吸引力。分子聚集导致C-C细胞的刚性增加,从而导致膜和水分加速流失,最终形成小球形红细胞。小球形红细胞具有最高的细胞内血红蛋白浓度,迅速经历细胞内结晶,并被网状内皮细胞隔离和破坏。