Randall T D, Heath A W, Santos-Argumedo L, Howard M C, Weissman I L, Lund F E
Trudeau Institute, Saranac Lake, New York 12983, USA.
Immunity. 1998 Jun;8(6):733-42. doi: 10.1016/s1074-7613(00)80578-6.
Despite extensive research, the role of CD40 signaling in B cell terminal differentiation remains controversial. Here we show that CD40 engagement arrests B cell differentiation prior to plasma cell formation. This arrest is manifested at a molecular level as a reduction in mRNA levels of secretory immunoglobulin gene products such as mu(s) and J chain as well as the loss of the transcriptional regulator BLIMP-1. Furthermore, the inhibition of B cell differentiation by CD40 engagement could not be overcome by either mitogens or cytokines, but could be reversed by antibodies that interfere with the CD40/gp39 interaction. These data suggest that secretory immunoglobulin is not produced by B cells that are actively engaged by gp39-expressing T cells.
尽管进行了广泛的研究,但CD40信号在B细胞终末分化中的作用仍存在争议。在此我们表明,CD40的激活在浆细胞形成之前阻止B细胞分化。这种阻止在分子水平上表现为分泌性免疫球蛋白基因产物(如μ(s)和J链)的mRNA水平降低以及转录调节因子BLIMP-1的缺失。此外,CD40激活对B细胞分化的抑制作用既不能被促有丝分裂原也不能被细胞因子克服,但可以被干扰CD40/gp39相互作用的抗体逆转。这些数据表明,表达gp39的T细胞积极作用的B细胞不会产生分泌性免疫球蛋白。