Transforming Growth Factor-alpha Null and Senescent Mice Show Decreased Neural Progenitor Cell Proliferation in the Forebrain Subependyma

The adult mammalian forebrain subependyma contains neural stem cells and their progeny, the constitutively proliferating progenitor cells. Using bromodeoxyuridine labeling to detect mitotically active cells, we demonstrate that the endogenous expression of transforming growth factor-alpha (TGFalpha)...

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Bibliographic Details
Published in:The Journal of neuroscience 1997-10, Vol.17 (20), p.7850-7859
Main Authors: Tropepe, Vincent, Craig, Constance G, Morshead, Cindi M, van der Kooy, Derek
Format: Article
Language:English
Subjects:
Aging - physiology
Animals
Cell Count
Cell Cycle
Cell Division
Cell Movement
Culture Techniques
Ependyma - cytology
Male
Mice
Mice, Knockout - genetics
Neurons - cytology
Neurons - physiology
Olfactory Bulb - cytology
Prosencephalon - cytology
Stem Cells - cytology
Time Factors
Transforming Growth Factor alpha - deficiency
Transforming Growth Factor alpha - genetics
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Summary:The adult mammalian forebrain subependyma contains neural stem cells and their progeny, the constitutively proliferating progenitor cells. Using bromodeoxyuridine labeling to detect mitotically active cells, we demonstrate that the endogenous expression of transforming growth factor-alpha (TGFalpha) is necessary for the full proliferation of progenitor cells localized to the dorsolateral corner of the subependyma and the full production of the neuronal progenitors that migrate to the olfactory bulbs. Proliferation of these progenitor cells also is diminished with age (in 23- to 25-months-old compared with 2- to 4-months-old mice), likely because of a lengthening of the cell cycle. Senescence or the absence of endogenous TGFalpha does not affect the numbers of neural stem cells isolated in vitro in the presence of epidermal growth factor. These results suggest that endogenous TGFalpha and the effects of senescence may regulate the proliferation of progenitor cells in the adult subependyma, but that the number of neural stem cells is maintained throughout life.
ISSN:0270-6474
1529-2401
DOI:10.1523/jneurosci.17-20-07850.1997