p53 is required for radiation-induced apoptosis in mouse thymocytes

Abstract

THE p53 tumour suppressor gene is the most widely mutated gene in human tumorigenesis^1,2. p53 encodes a transcriptional activator^3–7 whose _targets may include genes that regulate genomic stability^8,9, the cellular response to DNA damage^10,11, and cell-cycle progression^12,13. Introduction of wild-type p53 into cell lines that have lost endogenous p53 function can cause growth arrest^14–16 or induce a process of cell death known as apoptosis^17,18. During normal development, self-reactive thymocytes undergo negative selection by apoptosis¹⁹, which can also be induced in immature thymocytes by other stimuli, including exposure to glucocorticoids¹⁵ and ionizing radiation¹⁶. Although normal negative selection involves signalling through the T-cell receptor¹⁴, the induction of apoptosis by other stimuli is poorly understood. We have investigated the requirement for p53 during apoptosis in mouse thymocytes. We report here that immature thymocytes lacking p53 die normally when exposed to compounds that may mimic T-cell receptor engagement and to glucocorticoids but are resistant to the lethal effects of ionizing radiation. These results demonstrate that p53 is required for radiation-induced cell death in the thymus but is not necessary for all forms of apoptosis.