THE ROLE OF P53 IN SPONTANEOUS AND RADIATION-INDUCED APOPTOSIS IN THE GASTROINTESTINAL-TRACT OF NORMAL AND P53-DEFICIENT MICE

被引:1
|
作者
MERRITT, AJ
POTTEN, CS
KEMP, CJ
HICKMAN, JA
BALMAIN, A
LANE, DP
HALL, PA
机构
[1] CHRISTIE HOSP & HOLT RADIUM INST,NATL HLTH SERV TRUST,PATERSON INST CANC RES,CRC,MANCHESTER M20 9BX,LANCS,ENGLAND
[2] UNIV MANCHESTER,SCH BIOL SCI,CRC,MOLEC & CELLULAR PHARMACOL GRP,MANCHESTER M13 9PT,LANCS,ENGLAND
[3] BEATSON INST CANC RES,CRC,GLASGOW G61 1BD,SCOTLAND
[4] UNIV DUNDEE,DEPT PATHOL,DUNDEE DD1 4HN,SCOTLAND
[5] UNIV DUNDEE,DEPT BIOCHEM,CRC,CELL TRANSFORMAT UNIT,DUNDEE DD1 4HN,SCOTLAND
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:614 / 617
页数:4
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