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Ethylnitrosourea induces neural progenitor cell apoptosis after S-phase accumulation in a p53-dependent manner.
- Source :
-
Neurobiology of disease [Neurobiol Dis] 2005 Feb; Vol. 18 (1), pp. 218-25. - Publication Year :
- 2005
-
Abstract
- Neural progenitor cells populate the ventricular zone of the fetal central nervous system. In this study, immediately after the administration of ethylnitrosourea (ENU), an alkylating agent, an accumulation of neural progenitor cells in the S phase was observed. This event was caused by the inhibition or arrest of DNA replication rather than acceleration of the G1/S transition. Soon after this accumulation reached its peak, the number of cells in the G2/M phase decreased and the apoptotic cell count increased. In p53-deficient mice, both ENU-induced apoptosis and S-phase accumulation were almost completely abrogated. These findings indicate that ENU inhibits or arrests DNA replication in neural progenitor cells during the S phase and then evokes apoptosis before the cells enter the G2 phase. Furthermore, these data also demonstrate that both ENU-induced apoptosis and cell cycle perturbation in the S phase require p53.
- Subjects :
- Animals
Apoptosis physiology
Brain cytology
Brain drug effects
Brain embryology
Brain Neoplasms genetics
Brain Neoplasms metabolism
Cell Cycle drug effects
Cell Cycle physiology
Cell Transformation, Neoplastic genetics
Cell Transformation, Neoplastic metabolism
DNA Replication drug effects
DNA Replication physiology
Disease Models, Animal
Female
G2 Phase drug effects
G2 Phase physiology
Male
Mice
Mice, Knockout
Neurons drug effects
Neurons metabolism
Rats
Rats, Inbred F344
S Phase drug effects
S Phase physiology
Stem Cells metabolism
Apoptosis drug effects
Carcinogens pharmacology
Ethylnitrosourea pharmacology
Stem Cells drug effects
Tumor Suppressor Protein p53 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0969-9961
- Volume :
- 18
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Neurobiology of disease
- Publication Type :
- Academic Journal
- Accession number :
- 15649712
- Full Text :
- https://doi.org/10.1016/j.nbd.2004.09.015