Nagata S, Suda T
Osaka Bioscience Institute, Japan.
Immunol Today. 1995 Jan;16(1):39-43. doi: 10.1016/0167-5699(95)80069-7.
Fas ligand (FasL) is a death factor that binds to its receptor, Fas, and induces apoptosis. Two mutations that accelerate autoimmune disease, lpr and gld, are known to correspond to mutations within genes encoding Fas and FasL, respectively. Here, Shigekazu Nagata and Takashi Suda summarize current knowledge of Fas and FasL, and discuss the physiological role of the Fas system in T-cell development, cytotoxicity and cytotoxic T lymphocyte (CTL)-mediated autoimmune disease.
Fas配体(FasL)是一种死亡因子,它与其受体Fas结合并诱导细胞凋亡。已知两种加速自身免疫性疾病的突变,即lpr和gld,分别对应于编码Fas和FasL的基因内的突变。在这里,长谷川滋树和须田隆总结了关于Fas和FasL的当前知识,并讨论了Fas系统在T细胞发育、细胞毒性和细胞毒性T淋巴细胞(CTL)介导的自身免疫性疾病中的生理作用。