Nagata S
Osaka University Medical School, Japan.
Adv Exp Med Biol. 1996;406:119-24. doi: 10.1007/978-1-4899-0274-0_12.
Homeostasis in vertebrates is tightly regulated by cell death as well as by cell proliferation. The death of cells during embryogenesis, metamorphosis, endocrine-dependent tissue atrophy, and normal tissue turnover is "programmed cell death", mediated by a process called "apoptosis". Cytotoxic T lymphocytes and natural killer cells kill the target cells by inducing apoptosis. Apoptosis can be distinguished from necrosis, which occurs as a result of injury, complement attack, severe hypoxia and hyperthermia. Morphological and biochemical analyses of the apoptotic cell death process indicated that apoptosis is accompanied by condensation of cytoplasm, loss of plasma membrane microvilli, segmentation of nucleus, and extensive degradation of chromosomal DNA into oligomers of 180 bp. Cellular proliferation and differentiation are mediated by a family of proteins called cytokines. Our studies on the Fas ligand and Fas have indicated that apoptosis is also mediated by a cytokine and its receptor in some cases. Here, I summarize the current status of the Fas death factor system.
脊椎动物体内的稳态受到细胞死亡和细胞增殖的严格调控。胚胎发育、变态、内分泌依赖性组织萎缩以及正常组织更新过程中细胞的死亡是“程序性细胞死亡”,由一种称为“凋亡”的过程介导。细胞毒性T淋巴细胞和自然杀伤细胞通过诱导凋亡来杀死靶细胞。凋亡可与坏死相区分,坏死是由损伤、补体攻击、严重缺氧和高热引起的。对凋亡性细胞死亡过程的形态学和生化分析表明,凋亡伴随着细胞质浓缩、质膜微绒毛丧失、细胞核分割以及染色体DNA广泛降解为180bp的寡聚体。细胞增殖和分化由一类称为细胞因子的蛋白质介导。我们对Fas配体和Fas的研究表明,在某些情况下,凋亡也由一种细胞因子及其受体介导。在此,我总结Fas死亡因子系统的当前状况。