Stem cells and aging: expanding the possibilities

被引:280
作者
Rao, MS
Mattson, MP
机构
[1] NIA, Neurosci Lab, Gerontol Res Ctr 4F01, Baltimore, MD 21224 USA
[2] Univ Utah, Sch Med, Dept Neurobiol & Anat, Salt Lake City, UT 84132 USA
[3] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
关键词
Alzheimer's disease; apoptosis; brain; differentiation; endothelial; hematopoietic; neurons; Notch; telomerase;
D O I
10.1016/S0047-6374(01)00224-X
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In the very early stages of embryonic development, cells have the capability of dividing indefinately and then differentiating into any type of cell in the body. Recent studies have revealed that much of this remarkable developmental potential of embryonic stem cells is retained by small populations of cells within most tissues in the adult. Intercellular signals that control the proliferation, differentiation and survival of stem cells are being identified and include a diverse array of growth factors, cytokines and cell adhesion molecules. Intracellular mechanisms that regulate stem cell fate are also emerging and include established second messenger pathways, novel transcription factors and telomerase. The possibility that a decline in the numbers or plasticity of stem cell populations contributes to aging and age-related disease is suggested by recent findings. The remarkable plasticity of stem cells suggests that endogenous or transplanted stem cells can be 'tweaked' in ways that will allow them to replace lost or dysfunctional cell populations in diseases ranging from neurodegenerative and hematopoietic disorders to diabetes and cardiovascular disease. (C) 2001 Published by Elsevier Science Ireland Ltd.
引用
收藏
页码:713 / 734
页数:22
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