| Literature DB >> 32299851 |
Zhiwei Zhou1,2, Huabin He3,2, Kun Wang2, Xuyan Shi2, Yupeng Wang1,2, Ya Su2, Yao Wang4, Da Li2, Wang Liu1,2, Yongliang Zhang5, Lianjun Shen5, Weidong Han4, Lin Shen6, Jingjin Ding2,7, Feng Shao8,2,7,9.
Abstract
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.Entities:
Year: 2020 PMID: 32299851 DOI: 10.1126/science.aaz7548
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728