Layton J E, Vitetta E S, Uhr J W, Krammer P H
J Exp Med. 1984 Dec 1;160(6):1850-63. doi: 10.1084/jem.160.6.1850.
To gain insight into how T cell-derived lymphokines induce the secretion of IgG in activated B cells, we performed a limiting dilution analysis, using murine splenic B cells incubated with lipopolysaccharide (LPS) and a T cell-derived B cell differentiating factor for IgG (BCDF gamma)-containing supernatant (SN). The results of this analysis indicate that such a SN induces a marked increase in the precursor frequency of IgG1-secreting cells and a modest increase in clone size. The precursors lack surface IgG and are committed to the differentiation pathway for IgG1 secretion after LPS activation, but before the addition of BCDF gamma-containing SN. The majority of IgG1-secreting clones arise independently from precursors of cells that secrete IgG3. Taken together, these results indicate that BCDF gamma directs differentiation of activated B cells to IgG1 secretion.
为深入了解T细胞衍生的淋巴因子如何诱导活化B细胞分泌IgG,我们进行了有限稀释分析,使用与脂多糖(LPS)和含有T细胞衍生的IgG B细胞分化因子(BCDFγ)的上清液(SN)一起孵育的小鼠脾脏B细胞。该分析结果表明,这样的SN可诱导分泌IgG1的细胞前体频率显著增加,克隆大小适度增加。这些前体缺乏表面IgG,在LPS激活后但在添加含BCDFγ的SN之前就已确定进入IgG1分泌的分化途径。大多数分泌IgG1的克隆独立来源于分泌IgG3的细胞前体。综上所述,这些结果表明BCDFγ指导活化B细胞分化为分泌IgG1。