颗粒酶
上睑下垂
细胞毒性T细胞
颗粒酶A
颗粒酶B
穿孔素
细胞生物学
程序性细胞死亡
生物
化学
细胞凋亡
生物化学
体外
作者
Zhiwei Zhou,Huabin He,Kun Wang,Xuyan Shi,Yupeng Wang,Ya Su,Yao Wang,Da Li,Wang Liu,Yongliang Zhang,Lianjun Shen,Weidong Han,Lin Shen,Jingjin Ding,Feng Shao
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2020-04-16
卷期号:368 (6494)
被引量:1003
标识
DOI:10.1126/science.aaz7548
摘要
Cytotoxic lymphocyte-mediated immunity relies on granzymes. Granzymes are thought to kill target cells by inducing apoptosis, although the underlying mechanisms are not fully understood. Here, we report that natural killer cells and cytotoxic T lymphocytes kill gasdermin B (GSDMB)-positive cells through pyroptosis, a form of proinflammatory cell death executed by the gasdermin family of pore-forming proteins. Killing results from the cleavage of GSDMB by lymphocyte-derived granzyme A (GZMA), which unleashes its pore-forming activity. Interferon-γ (IFN-γ) up-regulates GSDMB expression and promotes pyroptosis. GSDMB is highly expressed in certain tissues, particularly digestive tract epithelia, including derived tumors. Introducing GZMA-cleavable GSDMB into mouse cancer cells promotes tumor clearance in mice. This study establishes gasdermin-mediated pyroptosis as a cytotoxic lymphocyte-killing mechanism, which may enhance antitumor immunity.
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