Wilson J W, Pritchard D M, Hickman J A, Potten C S
CRC Epithelial Biology Laboratory, Paterson Institute for Cancer Research, Manchester, United Kingdom.
Am J Pathol. 1998 Sep;153(3):899-909. doi: 10.1016/S0002-9440(10)65631-3.
p53-dependent expression of p21WAF-1/CIP1 has been studied in murine intestinal epithelium after exposure to ionizing radiation. In un-irradiated small intestine, neither p53 nor p21WAF-1/CIP1 could be detected by immunohistochemistry. After irradiation (8 Gy), there was a time- and dose-dependent increase in the expression of both proteins. In the small bowel, the positional expression of p53 and p21WAF-1/CIP1 was similar but not coincident. Both proteins could be observed throughout the crypts with greatest frequency of expression over the first 15 cell positions, which includes the stem cell population (approximately positions 3 to 5) and the proliferating, transit cell population (approximately positions 5 to 15). p53-positive cells were primarily distributed toward the base of the crypt relative to p21WAF-1/CIP1. Subdivision of the p53-positive cell population revealed that the cells with strongest p53 immunoreactivity were positioned farther toward the base of the crypt, and their distribution was approximately coincident with the frequency distribution of apoptotic cells. Cells that were either weakly or moderately immunoreactive for p53 were located toward the middle of the crypt and were approximately coincident with the distribution of p21WAF-1/CIP1. The numbers of both p53- and p21WAF-1/CIP1-positive cells declined steadily with time, and by 6 days after irradiation there were very few immunoreactive cells to observe. Radiation-induced increase in p53 and p21WAF-1/CIP1 expression was not detected in mice homozygously null for p53. Expression of p21WAF-1/CIP1 and incorporation of tritiated thymidine were found to be mutually exclusive. In the large bowel, p21WAF-1/CIP1 and p53 expression were observed along the entire length of the colonic crypts after irradiation (8 Gy), and, unlike in the small intestine, this expression was not only maintained but increased over 72 hours. p21WAF-1/CIP1 immunoreactivity was detected in large intestine epithelium up to 6 days after irradiation. The differential expression of p21WAF-1/CIP1, observed between the large and small bowel and within the small intestinal crypts, is discussed.
在暴露于电离辐射后的小鼠肠上皮中,对p21WAF-1/CIP1的p53依赖性表达进行了研究。在未受辐射的小肠中,通过免疫组织化学无法检测到p53和p21WAF-1/CIP1。辐射(8 Gy)后,两种蛋白的表达呈时间和剂量依赖性增加。在小肠中,p53和p21WAF-1/CIP1的定位表达相似但不重合。在整个隐窝中都能观察到这两种蛋白,在前15个细胞位置表达频率最高,这包括干细胞群体(大约位置3至5)和增殖的过渡细胞群体(大约位置5至15)。相对于p21WAF-1/CIP1,p53阳性细胞主要分布在隐窝底部。对p53阳性细胞群体的细分显示,p53免疫反应最强的细胞位于隐窝底部更远的位置,它们的分布与凋亡细胞的频率分布大致重合。对p53呈弱阳性或中等免疫反应的细胞位于隐窝中部,与p21WAF-1/CIP1的分布大致重合。p53和p21WAF-1/CIP1阳性细胞的数量均随时间稳步下降,照射后6天,几乎没有免疫反应性细胞可观察到。在p53基因纯合缺失的小鼠中未检测到辐射诱导的p53和p21WAF-1/CIP1表达增加。发现p21WAF-1/CIP1的表达与氚标记胸腺嘧啶的掺入相互排斥。在大肠中,照射(8 Gy)后沿结肠隐窝全长观察到p21WAF-1/CIP1和p53表达,与小肠不同的是,这种表达不仅持续存在,而且在72小时内增加。照射后6天内在大肠上皮中检测到p21WAF-1/CIP1免疫反应性。讨论了在大肠和小肠之间以及小肠隐窝内观察到 的p21WAF-1/CIP1的差异表达。