细胞毒性T细胞
颗粒酶
生物
脱颗粒
穿孔素
细胞毒性
溶解循环
细胞生物学
淋巴因子激活杀伤细胞
颗粒酶A
自然杀伤细胞
Fas配体
NK-92
免疫学
细胞凋亡
颗粒酶B
程序性细胞死亡
白细胞介素21
受体
体外
生物化学
病毒
作者
Isabel Prager,Carsten Watzl
标识
DOI:10.1002/jlb.mr0718-269r
摘要
Cellular cytotoxicity, the ability to kill other cells, is an important effector mechanism of the immune system to combat viral infections and cancer. Cytotoxic T cells and natural killer (NK) cells are the major mediators of this activity. Here, we summarize the cytotoxic mechanisms of NK cells. NK cells can kill virally infected of transformed cells via the directed release of lytic granules or by inducing death receptor-mediated apoptosis via the expression of Fas ligand or TRAIL. The biogenesis of perforin and granzymes, the major components of lytic granules, is a highly regulated process to prevent damage during the synthesis of these cytotoxic molecules. Additionally, NK cells have developed several strategies to protect themselves from the cytotoxic activity of granular content upon degranulation. While granule-mediated apoptosis is a fast process, death receptor-mediated cytotoxicity requires more time. Current data suggest that these 2 cytotoxic mechanisms are regulated during the serial killing activity of NK cells. As many modern approaches of cancer immunotherapy rely on cellular cytotoxicity for their effectiveness, unraveling these pathways will be important to further progress these therapeutic strategies.
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