Alvarez Sandra, Drané Pascal, Meiller Anne, Bras Marlene, Deguin-Chambon Valerie, Bouvard Veronique, May Evelyne
Commissariat à l'Energie Atomique (CEA), Centre National de la Recherche Scientifique (CNRS), Laboratoire de Cancérogenèse Moléculaire, 92265 Fontenay-aux-Roses Cedex, France.
Int J Radiat Biol. 2006 Nov;82(11):761-70. doi: 10.1080/09553000600949624.
Gamma-irradiation leads to activation of p53 tumour suppressor gene and to p53-dependant stimulation of a large panel of cellular genes including proapoptotic genes involved in intrinsic and extrinsic pathways. Most in vivo published data referred to high (lethal) irradiation doses. The present study was performed to analyse the p53-dependent response to more relevant low irradiation doses.
Mice were whole body exposed to irradiation doses decreasing from 5 - 0.05 Gy. Gene expression was estimated by real time reverse transcriptase polymerase chain reaction measurements on RNA extracted from thymus and spleen. Apoptosis was evaluated by the percentage of either annexin V positive or sub-G1 cells.
A 0.1 Gy irradiation dose already gives a significant stimulation of Puma (p53 up-regulated modulator of apoptosis), and 0.2 Gy of Bax (Bcl-2-associated X protein) and Killer/DR5 (Death Receptor 5). The expression of genes involved in the two apoptotic pathways was induced as soon as 1 h post-irradiation and reached a maximum at 3 h, the induction level depending on both the gene and the organ. A significant increase in the number of apoptotic cells is already detectable at 0.5 Gy with a maximum of induction at 6 h.
Our results reveal the high in vivo sensitivity of p53-dependent transcriptional activation of genes involved in the two main apoptotic pathways, their stimulation preceding the induction of apoptosis.
γ射线照射可导致p53肿瘤抑制基因激活,并通过p53依赖性刺激大量细胞基因,包括参与内源性和外源性途径的促凋亡基因。大多数已发表的体内研究数据涉及高(致死)照射剂量。本研究旨在分析p53对更相关的低照射剂量的依赖性反应。
对小鼠进行全身照射,照射剂量从5 Gy降至0.05 Gy。通过对从胸腺和脾脏提取的RNA进行实时逆转录聚合酶链反应测量来估计基因表达。通过膜联蛋白V阳性或亚G1期细胞的百分比评估细胞凋亡。
0.1 Gy的照射剂量已能显著刺激Puma(p53上调凋亡调节因子),0.2 Gy能刺激Bax(Bcl-2相关X蛋白)和Killer/DR5(死亡受体5)。参与两条凋亡途径的基因表达在照射后1小时即被诱导,并在3小时达到最大值,诱导水平取决于基因和器官。在0.5 Gy时即可检测到凋亡细胞数量显著增加,在6小时时诱导程度最高。
我们的结果揭示了参与两条主要凋亡途径的基因的p53依赖性转录激活在体内具有高度敏感性,它们的刺激先于细胞凋亡的诱导。