Merritt A J, Potten C S, Kemp C J, Hickman J A, Balmain A, Lane D P, Hall P A
CRC Department of Epithelial Biology, Paterson Institute for Cancer Research, Christie Hospital (NHS) Trust, Manchester, United Kingdom.
Cancer Res. 1994 Feb 1;54(3):614-7.
Three h after whole-body irradiation (8 Gy) of C57BL x DBA/2 F1 mice, p53 protein was expressed strongly in the stem cell compartment of the small intestine but at lower levels in the colon. At this time, apoptotic cells were also observed in the stem cell position of the small intestine, with fewer in the colon. In mice without copies of the p53 gene (nulls), the levels of spontaneous apoptosis, in both the small intestine and the colon, were not different from wild-type. Irradiation of the nulls with 8 Gy of gamma-rays failed to induce any further apoptosis: the loss of p53 essentially rendered the epithelial cells, from both the small intestine and the colon, radioresistant. The response of the epithelial stem cells of the small intestine suggests that p53 may play a role in the deletion of damaged cells with carcinogenic potential, whereas this process is limited in the colon.
对C57BL×DBA/2 F1小鼠进行全身照射(8 Gy)后3小时,p53蛋白在小肠干细胞区强烈表达,但在结肠中表达水平较低。此时,在小肠干细胞位置也观察到凋亡细胞,结肠中的凋亡细胞较少。在没有p53基因拷贝的小鼠(缺失型)中,小肠和结肠的自发凋亡水平与野生型没有差异。用8 Gy的γ射线照射缺失型小鼠未能诱导进一步的凋亡:p53的缺失基本上使小肠和结肠的上皮细胞具有抗辐射能力。小肠上皮干细胞的反应表明,p53可能在清除具有致癌潜力的受损细胞中发挥作用,而这一过程在结肠中受到限制。