But we next need to know which starting place will
migrate neurons to the area of need.
http://onlinelibrary.wiley.com/doi/10.1002/dneu.22028/abstract
Abstract
For more than a decade we have
known that the human brain harbours progenitor cells capable of becoming
mature neurons in the adult human brain. Since the original landmark
paper by Eriksson and colleagues in 1998 there have been many studies
investigating the effect depression, epilepsy, Alzheimer's disease,
Huntington's disease and Parkinson's disease have on the germinal zones
in the adult human brain. Of particular interest is the demonstration
that there are far fewer progenitor cells in the hippocampal subgranular
zone (SGZ) compared with the subventricular zone (SVZ) in the human
brain. Furthermore the quantity of progenitor cell proliferation in
human neurodegenerative diseases differs from that of animal models of
neurodegenerative diseases; there is minimal progenitor proliferation in
the SGZ and extensive proliferation in the SVZ in the human. In this
review we will present the data from a range of human and rodent studies
from which we can compare the amount of proliferation of cells in the
SVZ and SGZ in different neurodegenerative diseases.
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