目标2
炎症体
放射性损伤
DNA
程序性细胞死亡
DNA损伤
生物
细胞凋亡
炎症
医学
遗传学
免疫学
放射治疗
内科学
作者
Bo Hu,Chengcheng Jin,Huabing Li,Jiyu Tong,Xinshou Ouyang,Shu Zhu,Till Strowig,Chen Zhao,Jorge Henao‐Mejia,Katherine A. Fitzgerald,Stephanie C. Eisenbarth,Eran Elinav,Richard A. Flavell,Naniye Mallı Cetinbas,Fred C. Lam,Ömer Yılmaz
出处
期刊:Massachusetts Institute of Technology - DSpace@MIT
日期:2016-11-01
摘要
Acute exposure to ionizing radiation induces massive cell death and severe damage to tissues containing actively proliferating cells, including bone marrow and the gastrointestinal tract. However, the cellular and molecular mechanisms underlying this pathology remain controversial. Here, we show that mice deficient in the double-stranded DNA sensor AIM2 are protected from both subtotal body irradiation-induced gastrointestinal syndrome and total body irradiation-induced hematopoietic failure. AIM2 mediates the caspase-1-dependent death of intestinal epithelial cells and bone marrow cells in response to double-strand DNA breaks caused by ionizing radiation and chemotherapeutic agents. Mechanistically, we found that AIM2 senses radiation-induced DNA damage in the nucleus to mediate inflammasome activation and cell death. Our results suggest that AIM2 may be a new therapeutic target for ionizing radiation exposure.
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