Weitzman S, Margulies D H, Scharff M D
Ann Intern Med. 1976 Jul;85(1):110-6. doi: 10.7326/0003-4819-85-1-110.
Multiple myeloma raises a number of puzzling questions about the production of immunoglobulins and the malignant transformation of lymphoid cells. Some of these questions can be approached by studying mouse plasmacytomas and by genetic and biochemical studies of mouse myeloma cells in culture. The synthesis, assembly, glycosylation, and secretion of immunoglobulin has been analyzed in detail using the mouse myeloma system. The development of a technique that detects variants in clones of cultured mouse myeloma cells has led to the demonstration of a unique genetic instability in these cells. Based on these results a model is presented to explain the high frequency of ligh-chain producing (Bence Jones) myelomas in patients. Finally, mutant cell lines have been recovered which produce defective immunoglobulins similar to those found in heavy-chain disease and some other lymphoproliferative disorders.
多发性骨髓瘤引发了许多关于免疫球蛋白产生和淋巴细胞恶性转化的令人困惑的问题。其中一些问题可以通过研究小鼠浆细胞瘤以及对培养的小鼠骨髓瘤细胞进行遗传学和生物化学研究来解决。利用小鼠骨髓瘤系统已经对免疫球蛋白的合成、组装、糖基化和分泌进行了详细分析。一种检测培养的小鼠骨髓瘤细胞克隆中变体的技术的发展,已证明这些细胞具有独特的遗传不稳定性。基于这些结果,提出了一个模型来解释患者中产生轻链(本斯·琼斯蛋白)骨髓瘤的高频率。最后,已经获得了突变细胞系,这些细胞系产生有缺陷的免疫球蛋白,类似于在重链病和其他一些淋巴增殖性疾病中发现的免疫球蛋白。