Calame Kathryn
Department of Microbiology, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.
Curr Opin Immunol. 2008 Jun;20(3):259-64. doi: 10.1016/j.coi.2008.04.010. Epub 2008 Jun 12.
B lymphocyte induced maturation protein-1 (Blimp-1) mRNA is induced upon antigen-dependent activation of both T and B lymphocytes, in spite of the fact that it plays very different roles in the two lineages. B cells have at least four different mechanisms to repress Blimp-1 and repression is relieved before induction. Only one repressor, Bcl-6, is known in T cells. Activators must also be present to induce Blimp-1 in both T and B cells. Cytokines IL-21, IL-10, and IL-6, activating STAT3, are crucial in B cells along with toll-like receptor (TLR) signals, whereas IL-2 is crucial in T cells. AP-1, NF-kappaB, and IRF4 also activate Blimp-1.
B淋巴细胞诱导成熟蛋白-1(Blimp-1)mRNA在T淋巴细胞和B淋巴细胞的抗原依赖性激活过程中被诱导,尽管它在这两个细胞谱系中发挥着截然不同的作用。B细胞至少有四种不同的机制来抑制Blimp-1,并且在诱导之前抑制作用会解除。在T细胞中,已知只有一种阻遏物,即Bcl-6。在T细胞和B细胞中,也必须存在激活剂才能诱导Blimp-1。细胞因子IL-21、IL-10和IL-6激活STAT3,它们与Toll样受体(TLR)信号一起在B细胞中起关键作用,而IL-2在T细胞中起关键作用。AP-1、NF-κB和IRF4也可激活Blimp-1。