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Perspectives

Tumor Suppressor Dosage Regulates Stem Cell Dynamics during Aging

Catherine Gatza, Lynette Moore, Melissa Dumble and Lawrence A. Donehower

volume 6 | issue 1

1 January 2007
Pages: 52 - 55

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The ability of tissues to maintain homeostasis is dependent in part on the function of adult tissue stem cells, which have the capability to self-renew and differentiate into multiple lineages. It has been hypothesized that the ability of stem cells to maintain tissue homeostasis declines functionally with age and that this decline may account for many of the biological phenotypes associated with aging. Recently, tumor suppressors such as p53 have been implicated in both aging and the regulation of stem cell dynamics. Our recent findings suggest that p53 may impact hematopoietic stem cell (HSC) dynamics during mammalian aging.25 Utilizing mouse models of varying levels of p53 dosage, we have shown that alteration of p53 activity affects stem cell number, proliferation, and functionality with age. Several other recent studies have implicated other tumor suppressors in potential age-related regulation of HSC dynamics as well.30,37 These data support a model in which aging is caused in part by a decline in tissue stem cell regenerative function, regulated in part by tumor suppressors.

Authors

Catherine Gatza

Baylor College of Medicine; Houston TX, USA

Lynette Moore

Baylor College of Medicine; Houston TX, USA

Melissa Dumble

Baylor College of Medicine; Houston TX, USA

Lawrence A. Donehower

Baylor College of Medicine; Houston TX, USA



We now provide open access to journal articles published online for one year or more. This article may be downloaded at the following link:
 Download PDF

If the document does not open, please right-click on the link (control-click on a Macintosh) and select the option to save the file to disk.