P53 controls radiation-induced gastrointestinal syndrome in mice independent of apoptosis

David G. Kirsch, Philip M. Santiago, Emmanuelle Di Tomaso, Julie M. Sullivan, Wu Shiun Hou, Talya Dayton, Laura B. Jeffords, Pooja Sodha, Kim L. Mercer, Rhianna Cohen, Osamu Takeuchi, Stanley J. Korsmeyer, Roderick T. Bronson, Carla F. Kim, Kevin M. Haigis, Rakesh K. Jain, Tyler Jacks

Research output: Contribution to journalArticlepeer-review

199 Scopus citations


Acute exposure to ionizing radiation can cause lethal damage to the gastrointestinal (GI) tract, a condition called the GI syndrome. Whether the target cells affected by radiation to cause the GI syndrome are derived from the epithelium or endothelium and whether the target cells die by apoptosis or other mechanisms are controversial issues. Studying mouse models, we found that selective deletion of the proapoptotic genes Bak1 and Bax from the GI epithelium or from endothelial cells did not protect mice from developing the GI syndrome after sub-total-body gamma irradiation. In contrast, selective deletion of p53 from the GI epithelium, but not from endothelial cells, sensitized irradiated mice to the GI syndrome. Transgenic mice overexpressing p53 in all tissues were protected from the GI syndrome after irradiation. These results suggest that the GI syndrome is caused by the death of GI epithelial cells and that these epithelial cells die by a mechanism that is regulated by p53 but independent of apoptossis.

Original languageEnglish
Pages (from-to)593-596
Number of pages4
Issue number5965
StatePublished - 2010
Externally publishedYes


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