FKBP公司
细胞凋亡
体内
细胞生物学
Fas受体
体外
轻弹
程序性细胞死亡
Fas配体
化学
生物
癌症研究
生物化学
遗传学
作者
Seokhwi Kim,Jongpil Shin,Hyunsik Oh,Sangphil Ahn,Nury Kim,Won Do Heo
标识
DOI:10.1016/j.bbrc.2019.12.072
摘要
The inducible activation system is valuable for investigating spatiotemporal roles of molecules. A chemically inducible activation system for Fas (CD95/APO-1), which works efficiently to induce apoptosis and leads non-apoptotic pathways, has not yet been developed. Here, we engineered a rapamycin-induced dimerization system of Fas consisting of FKBP and FRB proteins. Treatment of rapamycin specifically induces cellular apoptosis. In neurons and cells with high c-FLIP expression, rapamycin-induced Fas activation triggered the activation of the non-apoptotic pathway components instead of cell death. Intracranial delivery of the system could be utilized to induce apoptosis of tumor cells upon rapamycin treatment. Our results demonstrate a novel inducible Fas activation system which operates with high efficiency and temporal precision in vitro and in vivo promising a potential therapeutic strategy.
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