Suzuki A, Tsutomi Y, Shimizu M, Matsuzawa A
Daiichi Pharmaceutical Co., Ltd., Drug Safety Research Laboratory, Tokyo R & D center 16-13, Kitakasai 1, Edogawa-ku, Tokyo 134, Japan.
Cell Death Differ. 1999 Jul;6(7):638-43. doi: 10.1038/sj.cdd.4400532.
The death receptor Fas transduces apoptotic death signaling upon stimulation with the Fas ligand. We previously reported that Fas contributes to vaginal cell death observed during the estrus cycle and after estrogen deprivation, using the functional Fas-lacking lpr and lprcg mutant mouse. In the present study, we investigated whether the Fas ligand also plays a dominant role in vaginal cell death using the functional Fas ligand-lacking gld mutant mouse. Our results demonstrated that vaginal cells of gld mice do not show any abnormalities, suggesting the possible presence of another ligand for Fas. Through our investigation, we demonstrated TNF-alpha as a ligand for vaginal Fas. Here, we propose that TNF-alpha acts for the ligand for Fas in vaginal cells, suggesting a new cell death induction system.
死亡受体Fas在受到Fas配体刺激时会转导凋亡性死亡信号。我们之前报道过,利用缺乏功能性Fas的lpr和lprcg突变小鼠,Fas参与了发情周期以及雌激素剥夺后观察到的阴道细胞死亡。在本研究中,我们使用缺乏功能性Fas配体的gld突变小鼠,研究Fas配体是否也在阴道细胞死亡中起主导作用。我们的结果表明,gld小鼠的阴道细胞没有显示出任何异常,这表明可能存在Fas的另一种配体。通过我们的研究,我们证明了TNF-α是阴道Fas的一种配体。在此,我们提出TNF-α作为阴道细胞中Fas的配体发挥作用,这提示了一种新的细胞死亡诱导系统。