The DNA-sensing AIM2 inflammasome controls radiation-induced cell death and tissue injury
dc.contributor.author | Hu, Bo | |
dc.contributor.author | Fitzgerald, Katherine A. | |
dc.contributor.author | Flavell, Richard A. | |
dc.date | 2022-08-11T08:08:20.000 | |
dc.date.accessioned | 2022-08-23T15:51:53Z | |
dc.date.available | 2022-08-23T15:51:53Z | |
dc.date.issued | 2016-11-11 | |
dc.date.submitted | 2017-05-22 | |
dc.identifier.citation | Science. 2016 Nov 11;354(6313):765-768. <a href="https://doi.org/10.1126/science.aaf7532">Link to article on publisher's site</a> | |
dc.identifier.issn | 0036-8075 (Linking) | |
dc.identifier.doi | 10.1126/science.aaf7532 | |
dc.identifier.pmid | 27846608 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14038/29010 | |
dc.description | <p>Full author list omitted for brevity. For the full list of authors, see article.</p> | |
dc.description.abstract | 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. | |
dc.language.iso | en_US | |
dc.relation | <a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=27846608&dopt=Abstract">Link to Article in PubMed</a> | |
dc.relation.url | https://doi.org/10.1126/science.aaf7532 | |
dc.subject | Immunology and Infectious Disease | |
dc.title | The DNA-sensing AIM2 inflammasome controls radiation-induced cell death and tissue injury | |
dc.type | Journal Article | |
dc.source.journaltitle | Science (New York, N.Y.) | |
dc.source.volume | 354 | |
dc.source.issue | 6313 | |
dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/faculty_pubs/1238 | |
dc.identifier.contextkey | 10195611 | |
html.description.abstract | <p>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.</p> | |
dc.identifier.submissionpath | faculty_pubs/1238 | |
dc.contributor.department | Program in Innate Immunity | |
dc.contributor.department | Department of Medicine, Division of Infectious Diseases and Immunology | |
dc.source.pages | 765-768 |