AffiliationEpithelial Biology Department, Paterson Institute for Cancer Research, Christie Hospital NHS Trust, Manchester M20 4BX.
MetadataShow full item record
AbstractMost organs of the body comprise populations of cells that are committed to specialized functions and that are renewed from small numbers of uncommitted progenitor or 'stem' cells. Stem cells are of central importance in the study of ageing because any senescent decline in the number or functional competence of stem cells will impair the capacity for renewal and turnover of committed cells, with potentially serious consequences for tissue homeostasis. The intestinal epithelium represents an excellent model system for the study of stem cells. Its spatial and hierarchical organisation allows the study of the function or characteristic of a given cell according to its position within the crypt. Hence, the stem cells which are located at the 4th-5th cell position from the bottom can be studied together with their daughter cells, as they divide and differentiate while migrating along the crypt-villus axis. The ability of the stem cells to undergo apoptosis and the capacity to regenerate the epithelium following injury were investigated in mice of different ages. Stem cells from older animals showed an increased apoptotic response following exposure to low doses of ionising radiation. The regenerative capacity was estimated by measuring the crypt survival levels and the growth rate of surviving crypts after high doses of irradiation. Surviving crypts in the older mice, suggesting an impairment in the damage recognition/response mechanisms, were both fewer and smaller than in young mice. The growth rate of surviving crypts was determined by measuring the crypt area and the number of cells/crypt at various times after 14 Gy irradiation. There was a growth delay of between half and one day in the older mice, and they subsequently grew more slowly. The number of cells susceptible to regenerate a crypt was also estimated. Surprisingly, they appear to be more numerous in the older mice. These studies indicate important age-related alterations in the capacity of the stem cells to regenerate the crypts after radiation-induced damage. The molecular bases of these changes are currently being investigated. Preliminary data showed alteration in the level of p53 and p21 expression, suggesting an age-related defect in the capacity to recognize damage and initiate apoptosis or repair.
CitationAgeing of murine small intestinal stem cells. 2001, 235:66-79; discussion 79-84, 101-4 Novartis Found. Symp.
JournalNovartis Foundation Symposium
- Altered stem cell regeneration in irradiated intestinal crypts of senescent mice.
- Authors: Martin K, Potten CS, Roberts SA, Kirkwood TB
- Issue date: 1998 Aug
- Age changes in stem cells of murine small intestinal crypts.
- Authors: Martin K, Kirkwood TB, Potten CS
- Issue date: 1998 Jun 15
- The relationship between ionizing radiation-induced apoptosis and stem cells in the small and large intestine.
- Authors: Potten CS, Grant HK
- Issue date: 1998 Oct
- Estimates of the number of clonogenic cells in crypts of murine small intestine.
- Authors: Potten CS, Hendry JH, Moore JV
- Issue date: 1987
- The effects of repeated doses of keratinocyte growth factor on cell proliferation in the cellular hierarchy of the crypts of the murine small intestine.
- Authors: Potten CS, O'Shea JA, Farrell CL, Rex K, Booth C
- Issue date: 2001 May