Pesando J M, Stucki M, Hoffman P
Division of Medical Oncology, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Hum Immunol. 1987 Aug;19(4):235-43. doi: 10.1016/0198-8859(87)90041-3.
Class II molecules of the major histocompatibility complex play an important role in mediating cellular interactions and are differentiation antigens on lymphobohematopoietic cells. We have previously characterized a human B-cell line (BALM-3) whose cells fail to express HLA class II molecules unless treated with phorbol acetate (TPA). Recently, we identified a spontaneous variant of BALM-3 whose cells express HLA class II molecules in the absence of TPA. Since normal B cells lose HLA class II molecules on terminal differentiation, these two BALM-3 cell populations may provide a model for a discrete phase of B-cell maturation. Alternatively, they may reflect two B-cell activation states characterized by quantitative differences in their expression of class II molecules. Expression of six of 22 additional surface molecules (HLA class I, CD23, p60, p124, p129, p141) increases by a factor of three or more as BALM-3 cells spontaneously acquire class II molecules while that of one of the 22 (p45) decreases by a comparable amount. Expression of the plasma cell-associated T10/CD38 antigen decreases by a factor of two. These additional surface molecules might also reflect lymphoid differentiation/activation antigens and/or participate in HLA class II-mediated cellular interactions and require further study. Use of TPA to induce the expression of HLA class II molecules produces similar changes in several but not all of these surface antigens.
主要组织相容性复合体的II类分子在介导细胞间相互作用中起重要作用,并且是淋巴造血细胞上的分化抗原。我们之前鉴定了一种人类B细胞系(BALM - 3),其细胞除非用佛波酯(TPA)处理,否则无法表达HLA II类分子。最近,我们鉴定出BALM - 3的一个自发变体,其细胞在没有TPA的情况下表达HLA II类分子。由于正常B细胞在终末分化时会丢失HLA II类分子,这两种BALM - 3细胞群体可能为B细胞成熟的一个离散阶段提供模型。或者,它们可能反映了两种B细胞激活状态,其特征在于II类分子表达的定量差异。随着BALM - 3细胞自发获得II类分子,22种额外表面分子中的6种(HLA I类、CD23、p60、p124、p129、p141)的表达增加了三倍或更多,而22种中的一种(p45)的表达则下降了相当的量。浆细胞相关的T10/CD38抗原的表达下降了两倍。这些额外的表面分子也可能反映淋巴样分化/激活抗原和/或参与HLA II类介导的细胞间相互作用,需要进一步研究。使用TPA诱导HLA II类分子的表达会在几种但不是所有这些表面抗原中产生类似的变化。