Literature DB >> 9792141

The relationship between ionizing radiation-induced apoptosis and stem cells in the small and large intestine.

C S Potten1, H K Grant.   

Abstract

Apoptosis is observed in the crypts of the small intestine of healthy animals and man (spontaneous apoptosis). The levels can be dramatically elevated 3-6 h following ionizing radiation exposure. Both the spontaneous and radiation-induced apoptosis in the small intestine crypts are most frequently observed at the positions in the crypt associated with stem cells (about four cell positions from the base of the crypt). The number of apoptotic deaths can be counted in routine histological preparations, but interpretation of the counts is complicated by numerous factors. However, recording the number of cells containing one or more apoptotic fragments in crypt sections provides a good estimate for the absolute number of cell deaths in crypts. Similarities are noted in the frequency and cell positional relationship of radiation-induced apoptosis in the small intestine of various strains of mice and one strain of rat. Apoptosis in the large intestine is generally lower in frequency than in the small intestine and, for the mid-colonic and rectal regions, has a different cell positional frequency distribution, with the highest apoptotic yield at the crypt base. The caecal colon has a pattern of apoptotic distribution more similar to that in the small intestine. After exposure to 1 Gy ionizing radiation, the maximum apoptotic yield occurs over a period of 3-6 h in the small intestine. There is some unexplained variability in the values between groups of mice and between different mouse strains. After 8 Gy, the yield remains elevated for several days, however a similar maximum yield is still observed at the early times. In mouse large intestine and rat small intestine, the yield continues to rise until about 6 Gy in mouse large intestine and until at least 10 Gy in rat small intestine. Spontaneous apoptosis is interpreted as part of the homeostatic mechanism regulating stem cell numbers. About 1.6 cells per crypt are dying at any one time. Following irradiation, there is an apparent relationship between mitotic and apoptotic levels, suggesting that these processes are linked. The dose-response relationship suggests that there are about six apoptosis-susceptible cells in crypts of the small intestine, with about 2-4 of these occurring at cell positions in which there are other more resistant clonogenic cells. In the large intestine, the position of these apoptosis-susceptible cells varies with region, but the numbers are similar.

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Mesh:

Year:  1998        PMID: 9792141      PMCID: PMC2063142          DOI: 10.1038/bjc.1998.618

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  31 in total

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Authors:  C S Potten
Journal:  Cancer Metastasis Rev       Date:  1992-09       Impact factor: 9.264

2.  A model of the control of cellular regeneration in the intestinal crypt after perturbation based solely on local stem cell regulation.

Authors:  U Paulus; C S Potten; M Loeffler
Journal:  Cell Prolif       Date:  1992-11       Impact factor: 6.831

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Authors:  H R Withers; M M Elkind
Journal:  Int J Radiat Biol Relat Stud Phys Chem Med       Date:  1970

4.  Cell migration in the small and large bowel shows a strong circadian rhythm.

Authors:  J M Qiu; S A Roberts; C S Potten
Journal:  Epithelial Cell Biol       Date:  1994

5.  The role of p53 in spontaneous and radiation-induced apoptosis in the gastrointestinal tract of normal and p53-deficient mice.

Authors:  A J Merritt; C S Potten; C J Kemp; J A Hickman; A Balmain; D P Lane; P A Hall
Journal:  Cancer Res       Date:  1994-02-01       Impact factor: 12.701

6.  Deduction of the clonogen content of intestinal crypts: a direct comparison of two-dose and multiple-dose methodologies.

Authors:  S A Roberts; J H Hendry; C S Potten
Journal:  Radiat Res       Date:  1995-03       Impact factor: 2.841

7.  Target cells for the cytotoxic effects of carcinogens in the murine small bowel.

Authors:  Y Q Li; C Y Fan; P J O'Connor; D J Winton; C S Potten
Journal:  Carcinogenesis       Date:  1992-03       Impact factor: 4.944

8.  A possible explanation for the differential cancer incidence in the intestine, based on distribution of the cytotoxic effects of carcinogens in the murine large bowel.

Authors:  C S Potten; Y Q Li; P J O'Connor; D J Winton
Journal:  Carcinogenesis       Date:  1992-12       Impact factor: 4.944

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10.  Differential expression of bcl-2 in intestinal epithelia. Correlation with attenuation of apoptosis in colonic crypts and the incidence of colonic neoplasia.

Authors:  A J Merritt; C S Potten; A J Watson; D Y Loh; K Nakayama; K Nakayama; J A Hickman
Journal:  J Cell Sci       Date:  1995-06       Impact factor: 5.285

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  68 in total

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2.  Intestinal crypt clonogens: a new interpretation of radiation survival curve shape and clonogenic cell number.

Authors:  S A Roberts; J H Hendry; C S Potten
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3.  Investigation of Musashi-1 expressing cells in the murine model of dextran sodium sulfate-induced colitis.

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4.  Establishment of a long-term culture system for rat colon epithelial cells.

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5.  An enteroendocrine cell-based model for a quiescent intestinal stem cell niche.

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Review 6.  Association between radiation-induced cell death and clinically relevant radioresistance.

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7.  Effect of fat feeding on pro-oxidant and anti-oxidant enzyme systems in rat intestine: possible role in the turnover of enterocytes.

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Journal:  Dig Dis Sci       Date:  2008-11-07       Impact factor: 3.199

8.  Paradoxical Roles of Elongation Factor-2 Kinase in Stem Cell Survival.

Authors:  Yi Liao; Hsueh-Ping Chu; Zhixian Hu; Jason J Merkin; Jianmin Chen; Zuguo Liu; Kurt Degenhardt; Eileen White; Alexey G Ryazanov
Journal:  J Biol Chem       Date:  2016-07-27       Impact factor: 5.157

9.  The stem cells of small intestinal crypts: where are they?

Authors:  C S Potten; R Gandara; Y R Mahida; M Loeffler; N A Wright
Journal:  Cell Prolif       Date:  2009-09-28       Impact factor: 6.831

10.  The radioprotective effects of the hexane and ethyl acetate extracts of Callophyllis japonica in mice that undergo whole body irradiation.

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