Author: Tower J.
Affiliation:
Molecular and Computational Biology Program, University of Southern California, Los Angeles, CA, USA. jtower@usc.edu.
Conference/Journal: Wiley Interdiscip Rev Dev Biol.
Date published: 2012 Nov
Other:
Volume ID: 1 , Issue ID: 6 , Pages: 789-802 , Special Notes: doi: 10.1002/wdev.56 , Word Count: 206
The unique properties and functions of stem cells make them particularly susceptible to stresses and also lead to their regulation by stress. Stem cell division must respond to the demand to replenish cells during normal tissue turnover as well as in response to damage. Oxidative stress, mechanical stress, growth factors, and cytokines signal stem cell division and differentiation. Many of the conserved pathways regulating stem cell self-renewal and differentiation are also stress-response pathways. The long life span and division potential of stem cells create a propensity for transformation (cancer) and specific stress responses such as apoptosis and senescence act as antitumor mechanisms. Quiescence regulated by CDK inhibitors and a hypoxic niche regulated by FOXO transcription factor function to reduce stress for several types of stem cells to facilitate long-term maintenance. Aging is a particularly relevant stress for stem cells, because repeated demands on stem cell function over the life span can have cumulative cell-autonomous effects including epigenetic dysregulation, mutations, and telomere erosion. In addition, aging of the organism impairs function of the stem cell niche and systemic signals, including chronic inflammation and oxidative stress. WIREs Dev Biol 2012 doi: 10.1002/wdev.56 For further resources related to this article, please visit the WIREs website.
Copyright © 2012 Wiley Periodicals, Inc.
PMID: 23799624