Age changes in stem cells of murine small intestinal crypts

被引:100
作者
Martin, K
Kirkwood, TBL
Potten, CS
机构
[1] Univ Manchester, Dept Geriatr Med, Biol Gerontol Grp, Manchester M13 9PT, Lancs, England
[2] Univ Manchester, Sch Biol Sci, Manchester M13 9PT, Lancs, England
[3] Christie Hosp NHS Trust, CRC, Dept Epithelial Biol, Paterson Inst Canc Res, Manchester M20 4BX, Lancs, England
关键词
ageing; stem cells; small intestine; apoptosis;
D O I
10.1006/excr.1998.4001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cell senescence is seen in many types of differentiated cells but age changes in stem cells have not previously been clearly demonstrated. Changes in stem cells may be of great importance for the ageing process, because any decline with age in the numbers and functional integrity of stem cells can lead to progressive deterioration of function and of proliferative homeostasis in tissues. Stem cells of the murine small intestine provide an excellent model system because these cells occupy a well-defined position near the base of the crypts of Lieberkuhn. We examined mice aged between 5 and 32 months and found age-related alterations in the histology of the small intestine and in the apoptotic response of stem cells to low-dose irradiation. Apoptosis in the crypts is concentrated around the stem cell position and can be markedly elevated by exposure to radiation or cytotoxic agents, suggesting that "suicide" of damaged stem cells may be an important system for long-term tissue maintenance. Animals aged 5, 15, 18, and 29 months were exposed to either 1 or 8 Gy gamma irradiation. A twofold increase in the level of apoptosis was seen following 1 Gy gamma irradiation in the 29-month-old animals, compared to the young and middle-age groups. After 8 Gy irradiation the level of apoptosis in all age groups was high and the age effect less pronounced. The data suggest that stem cells do undergo some functional alteration with age. (C) 1998 Academic Press.
引用
收藏
页码:316 / 323
页数:8
相关论文
共 40 条
[31]   What is an apoptotic index measuring? A commentary [J].
Potten, CS .
BRITISH JOURNAL OF CANCER, 1996, 74 (11) :1743-1748
[32]   THE SIGNIFICANCE OF SPONTANEOUS AND INDUCED APOPTOSIS IN THE GASTROINTESTINAL-TRACT OF MICE [J].
POTTEN, CS .
CANCER AND METASTASIS REVIEWS, 1992, 11 (02) :179-195
[33]  
POTTEN CS, 1997, IN PRESS J EXP PATHO
[34]   DEDUCTION OF THE CLONOGEN CONTENT OF INTESTINAL CRYPTS - A DIRECT COMPARISON OF 2-DOSE AND MULTIPLE-DOSE METHODOLOGIES [J].
ROBERTS, SA ;
HENDRY, JH ;
POTTEN, CS .
RADIATION RESEARCH, 1995, 141 (03) :303-308
[35]  
ROWLATT C, 1976, Laboratory Animals (London), V10, P419, DOI 10.1258/002367776780956917
[36]   Replicative senescence: Implications for in vivo aging and tumor suppression [J].
Smith, JR ;
PereiraSmith, OM .
SCIENCE, 1996, 273 (5271) :63-67
[37]  
WANG E, 1995, CANCER RES, V55, P2284
[38]  
WEBSTER S G P, 1975, Age and Ageing, V4, P168, DOI 10.1093/ageing/4.3.168
[39]   SENESCENCE OF AN ANTIBODY-FORMING CELL CLONE [J].
WILLIAMSON, AR ;
ASKONAS, BA .
NATURE, 1972, 238 (5363) :337-+
[40]   MICROCOLONY SURVIVAL ASSAY FOR CELLS OF MOUSE INTESTINAL MUCOSA EXPOSED TO RADIATION [J].
WITHERS, HR ;
ELKIND, MM .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY AND RELATED STUDIES IN PHYSICS CHEMISTRY AND MEDICINE, 1970, 17 (03) :261-&