Polla B S, Poljak A, Ohara J, Paul W E, Glimcher L H
J Immunol. 1986 Nov 15;137(10):3332-7.
We have analyzed the mechanism of action of BSF-1 on class II gene expression in two murine pre-B cell lines that are at different stages of differentiation. In vitro transcription assays demonstrated that BSF-1 induced rapid transcription of class II genes within 1 hr by a mechanism that was independent of protein synthesis. Although cell surface expression of class II was detectable by 2 hr after induction and persisted for up to 96 hr after removal of BSF-1, levels of class II-specific mRNA and density of cell surface class II increased to a maximum between 24 and 72 hr after induction. Furthermore, prostaglandin E2 prevented the induction of class II gene expression by BSF-1. The effects of BSF-1 are unlikely to be mediated through calcium fluxes or activation of protein kinase C, since treatment with agents such as PMA and the calcium ionophore A23187 did not result in expression of class II molecules. Other lymphokines, such as IFN-gamma, IL 1, IL 2, and IL 3, did not affect class II gene expression in these two cell lines. These data provide further insight into the mechanisms by which class II gene expression is regulated in B cells.
我们分析了BSF-1在两种处于不同分化阶段的小鼠前B细胞系中对II类基因表达的作用机制。体外转录试验表明,BSF-1通过一种独立于蛋白质合成的机制在1小时内诱导II类基因快速转录。虽然诱导后2小时可检测到II类分子的细胞表面表达,且在去除BSF-1后可持续长达96小时,但II类特异性mRNA水平和细胞表面II类分子密度在诱导后24至72小时之间增加到最大值。此外,前列腺素E2可阻止BSF-1诱导II类基因表达。BSF-1的作用不太可能通过钙通量或蛋白激酶C的激活来介导,因为用PMA和钙离子载体A23187等试剂处理不会导致II类分子的表达。其他淋巴因子,如IFN-γ、IL-1、IL-2和IL-3,对这两种细胞系中的II类基因表达没有影响。这些数据为B细胞中II类基因表达的调控机制提供了进一步的见解。