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dc.contributor.authorHu, Bo
dc.contributor.authorFitzgerald, Katherine A.
dc.contributor.authorFlavell, Richard A.
dc.date2022-08-11T08:08:20.000
dc.date.accessioned2022-08-23T15:51:53Z
dc.date.available2022-08-23T15:51:53Z
dc.date.issued2016-11-11
dc.date.submitted2017-05-22
dc.identifier.citationScience. 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.issn0036-8075 (Linking)
dc.identifier.doi10.1126/science.aaf7532
dc.identifier.pmid27846608
dc.identifier.urihttp://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.abstractAcute 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.isoen_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.urlhttps://doi.org/10.1126/science.aaf7532
dc.subjectImmunology and Infectious Disease
dc.titleThe DNA-sensing AIM2 inflammasome controls radiation-induced cell death and tissue injury
dc.typeJournal Article
dc.source.journaltitleScience (New York, N.Y.)
dc.source.volume354
dc.source.issue6313
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/1238
dc.identifier.contextkey10195611
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.submissionpathfaculty_pubs/1238
dc.contributor.departmentProgram in Innate Immunity
dc.contributor.departmentDepartment of Medicine, Division of Infectious Diseases and Immunology
dc.source.pages765-768


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