Glassy M C, Ferrone S
Am J Pathol. 1981 Apr;103(1):1-9.
The ultrastructure of three human lymphoblastoid B cell lines, Raji, RPMI 4098, and WIL-2, was analyzed after the cells were incubated with tunicamycin, and antibiotic that selectively inhibits N-linked glycosylation of macromolecules. After a 24-hour exposure to 1.0 microgram/ml of tunicamycin, the lymphocytes lose their microvilli and become smooth spheres or develop a few blebs. Also, the cells show a dilation of the endoplasmic reticulum and an increase in myelin figures resulting from intracellular membrane accumulation, possibly lysosomal in origin. These ultrastructural alterations are similar to those observed in Tay-Sachs, Fabrey's, and Gaucher's diseases, Type II pneumocytes in viral pneumonitis, certain lysosomal storage diseases, and in aging fibroblasts. Therefore, tunicamycin-treated cells may be a useful model in the correlation of altered ultrastructural pattern in membrane flow with the etiology of certain diseases.
将三种人类淋巴母细胞样B细胞系Raji、RPMI 4098和WIL-2与衣霉素(一种选择性抑制大分子N-连接糖基化的抗生素)一起孵育后,对其超微结构进行了分析。在暴露于1.0微克/毫升衣霉素24小时后,淋巴细胞失去微绒毛,变成光滑的球体或出现一些泡状突起。此外,细胞显示内质网扩张,并且由于细胞内膜积累(可能起源于溶酶体)导致髓鞘样结构增多。这些超微结构改变类似于在泰-萨克斯病、法布里病、高雪氏病、病毒性肺炎中的II型肺泡上皮细胞、某些溶酶体贮积病以及衰老的成纤维细胞中观察到的改变。因此,经衣霉素处理的细胞可能是一种有用的模型,用于关联膜流中超微结构模式改变与某些疾病的病因。