Ninomiya-Tsuji J, Torti F M, Ringold G M
Affymax Research Institute, Palo Alto, CA 94304.
Proc Natl Acad Sci U S A. 1993 Oct 15;90(20):9611-5. doi: 10.1073/pnas.90.20.9611.
Tumor necrosis factor (TNF) inhibits and reverses differentiation of mouse adipogenic TA1 cells. We have found that TNF induces c-myc in a sustained manner in both preadipocytes and adipocytes; in contrast, serum induces c-myc transiently and only in preadipocytes. This TNF-mediated c-myc induction is not coupled with cell proliferation but is correlated with TNF-mediated inhibition of adipocyte differentiation. We prepared an inducible c-myc transformant of TA1 cells by transfection of the mouse c-myc gene under the control of the metallothionein-I promoter. These cells are unable to differentiate to adipocytes in the presence of Zn2+/Cd2+, and in differentiated TA1 cells, Zn2+/Cd2+ causes reduction of adipocyte-specific gene expression as does TNF. Lastly, exposure of TA1 cells to antisense c-myc oligonucleotide partially blocked the TNF-mediated reduction of adipocyte-specific gene expression. Thus, TNF-mediated c-myc expression is distinct in character from that involved in mitogenic responses but appears to play an important role in inhibition and reversal of adipocyte differentiation.
肿瘤坏死因子(TNF)抑制并逆转小鼠脂肪生成TA1细胞的分化。我们发现,TNF在脂肪前体细胞和脂肪细胞中持续诱导c-myc;相比之下,血清仅在脂肪前体细胞中短暂诱导c-myc。这种TNF介导的c-myc诱导与细胞增殖无关,但与TNF介导的脂肪细胞分化抑制相关。我们通过在金属硫蛋白-I启动子控制下转染小鼠c-myc基因,制备了TA1细胞的可诱导c-myc转化体。在存在Zn2+/Cd2+的情况下,这些细胞无法分化为脂肪细胞,并且在分化的TA1细胞中,Zn2+/Cd2+与TNF一样导致脂肪细胞特异性基因表达降低。最后,将TA1细胞暴露于反义c-myc寡核苷酸可部分阻断TNF介导的脂肪细胞特异性基因表达降低。因此,TNF介导的c-myc表达在性质上与有丝分裂反应中涉及的表达不同,但似乎在抑制和逆转脂肪细胞分化中起重要作用。