Abstract
Stem cells have defining properties that are suited for tissue homeostasis and repair, but a central issue is how these cells generate mature cell types without exhausting their capacity for self-renewal. This chapter focuses on the central nervous system (CNS) to exemplify the regulation of adult stem cell self-renewal in the service of organ function. Topics will include conventional and novel methods used to distinguish stem cells from other proliferating cell types and the pitfalls in attempting to precisely characterize stem cell function. These methods reveal that stem cells interpret multiple signals to control the balance of self-renewal and quiescence. Among the emerging themes is that stem cell self-renewal is dynamically regulated throughout life, is integrally connected with lineage specification, and reflects a conservation of many intrinsic and extrinsic mechanisms from fetal development.
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- AraC:
-
Cytosine arabinoside
- BMP:
-
Bone morphogenetic proteins
- BrdU:
-
5-Bromo-2-deoxyuridine
- EGF:
-
Epidermal growth factor
- FGF2:
-
Fibroblast growth factor 2
- Fox:
-
Forkhead winged helix family proteins
- GFAP:
-
Glial fibrillary acidic protein
- GFP:
-
Green fluorescent protein
- IPC:
-
Intermediate progenitor cell
- NB:
-
Neuroblast
- NSC:
-
Neural stem cell
- SVZ:
-
Subventricular zone
- SGZ:
-
Subgranular zone
- Shh:
-
Sonic hedgehog
- Wnt:
-
Wingless/Int homolog proteins
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Panchision, D.M. (2011). Molecular Mechanisms Regulating Adult Stem Cell Self-Renewal. In: Phinney, D. (eds) Adult Stem Cells. Stem Cell Biology and Regenerative Medicine. Humana Press. https://doi.org/10.1007/978-1-61779-002-7_1
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