Lin Y, Wong K, Calame K
Department of Microbiology, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.
Science. 1997 Apr 25;276(5312):596-9. doi: 10.1126/science.276.5312.596.
Transcription of c-myc in plasma cells, which are terminally differentiated B cells, is repressed by plasmacytoma repressor factor. This factor was identified as Blimp-1, known for its ability to induce B cell differentiation. Blimp-1 repressed c-myc promoter activity in a binding site-dependent manner. Treatment of BCL1 lymphoma cells with interleukin-2 (IL-2) plus IL-5 induced Blimp-1 and caused a subsequent decline in c-Myc protein. Ectopic expression of Blimp-1 in Abelson-transformed precursor B cells repressed endogenous c-Myc and caused apoptosis; Blimp-1-induced death was partially overcome by ectopic expression of c-Myc. Thus, repression of c-myc is a component of the Blimp-1 program of terminal B cell differentiation.
浆细胞(即终末分化的B细胞)中c-myc的转录受浆细胞瘤抑制因子的抑制。该因子被鉴定为Blimp-1,它以诱导B细胞分化的能力而闻名。Blimp-1以结合位点依赖的方式抑制c-myc启动子活性。用白细胞介素-2(IL-2)加白细胞介素-5处理BCL1淋巴瘤细胞可诱导Blimp-1表达,随后导致c-Myc蛋白水平下降。在阿贝尔逊转化的前体B细胞中异位表达Blimp-1可抑制内源性c-Myc并导致细胞凋亡;c-Myc的异位表达可部分克服Blimp-1诱导的细胞死亡。因此,抑制c-myc是Blimp-1介导的终末B细胞分化程序的一个组成部分。