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First published online 16 August 2006
doi: 10.1242/dev.02541
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1 Department of Neuroscience, McKnight Brain Institute, University of Florida,
Gainesville, FL 32610, USA.
2 Shands Cancer Center, University of Florida, Gainesville, FL 32610, USA.
3 Department of Neurosurgery, University of Florida, Gainesville, FL 32610,
USA.
4 Department of Molecular Genetics and Microbiology University of Florida,
Gainesville, FL 32610, USA.
5 Program in Stem Cell Biology and Regenerative Medicine, University of Florida,
Gainesville, FL 32610, USA.
Author for correspondence (e-mail:
steindler{at}mbi.ufl.edu)
Accepted 6 July 2006
The isolation and expansion of human neural cell types has become
increasingly relevant in restorative neurobiology. Although embryonic and
fetal tissue are frequently envisaged as providing sufficiently primordial
cells for such applications, the developmental plasticity of endogenous adult
neural cells remains largely unclear. To examine the developmental potential
of adult human brain cells, we applied conditions favoring the growth of
neural stem cells to multiple cortical regions, resulting in the
identification and selection of a population of adult human neural progenitors
(AHNPs). These nestin+ progenitors may be derived from multiple
forebrain regions, are maintainable in adherent conditions, co-express
multiple glial and immature markers, and are highly expandable, allowing a
single progenitor to theoretically form sufficient cells for
4x107 adult brains. AHNPs longitudinally maintain the
ability to generate both glial and neuronal cell types in vivo and in vitro,
and are amenable to genetic modification and transplantation. These findings
suggest an unprecedented degree of inducible plasticity is retained by cells
of the adult central nervous system.
Key words: Astrocyte, Progenitor, Plasticity, Human, Expansion, Commitment, Transplantation
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