Stashenko P, Nadler L M, Hardy R, Schlossman S F
Proc Natl Acad Sci U S A. 1981 Jun;78(6):3848-52. doi: 10.1073/pnas.78.6.3848.
The fate of two recently described human B lymphocyte-specific antigens (B1 and B2) was studied after B-cell activation in vivo and in vitro. Whereas both B1 and B2 were present on virtually all B cells from normal lymph nodes, B2 was absent from approximately 50% of B cells from hyperplastic lymph nodes. When B cells from spleen, tonsil, or peripheral blood were stimulated in vitro with pokeweed mitogen, activated cells were found to lose B2 (days 4-5) and subsequently B1 (days 6-7). Temporally, B2 loss was accompanied by loss of surface IgD, expression of T10, and the development of intracytoplasmic IgM; B1 loss was correlated with the acquisition of surface IgG and the appearance of intracytoplasmic IgG. Peripheral blood B cells, on which B2 is normally only weakly expressed (B1++++B2+) in contrast to B cells from secondary lymphoid organs (B1++++B2++), exhibited a transitory increase in B2 expression to the B1++++B2++ phenotype prior to B2 disappearance during activation. Taken together with other findings, this observation suggests that peripheral blood may contain a relatively immature subpopulation of B cells.
在体内和体外对两种最近描述的人类B淋巴细胞特异性抗原(B1和B2)在B细胞活化后的命运进行了研究。虽然B1和B2几乎存在于正常淋巴结的所有B细胞上,但增生性淋巴结中约50%的B细胞不存在B2。当用商陆有丝分裂原在体外刺激脾脏、扁桃体或外周血中的B细胞时,发现活化细胞在第4 - 5天失去B2,随后在第6 - 7天失去B1。在时间上,B2的丢失伴随着表面IgD的丢失、T10的表达以及胞浆内IgM的出现;B1的丢失与表面IgG的获得以及胞浆内IgG的出现相关。与来自二级淋巴器官的B细胞(B1++++B2++)相比,外周血B细胞上的B2通常仅微弱表达(B1++++B2+),在活化过程中B2消失之前,其B2表达短暂增加至B1++++B2++表型。结合其他发现,这一观察结果表明外周血可能含有相对不成熟的B细胞亚群。