Multipotent neural progenitor cells (NPCs) may someday be utilized to treat many neurological disorders. NPCs are self-renewing, differentiate into all major neuronal lineages, and may possess the ability to integrate into and replace degenerated regions of the brain. Development of effective NPC-based cell replacement will require a greater understanding of the determinants that influence NPC proliferation and differentiation. Preliminary studies in our laboratory have demonstrated that the transcriptional repressor Hes6 (Hairy/Enhancer of Slipt 6) enhances neuronal differentiation of murine embryonic NPCs.
The specific aims of this proposal will investigate the post-translational regulation of Hes6 expression, and determine how components of the Notch signaling pathway (including Hes1 and Mash1) influence the ability of Hes6 to promote differentiation in NPCs.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32NS047048-02
Application #
6795887
Study Section
Special Emphasis Panel (ZRG1-F03A (20))
Program Officer
Leblanc, Gabrielle G
Project Start
2003-07-17
Project End
2006-07-16
Budget Start
2004-07-17
Budget End
2005-07-16
Support Year
2
Fiscal Year
2004
Total Cost
$47,296
Indirect Cost
Name
University of Iowa
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Harper, Scott Q; Staber, Patrick D; Beck, Christine R et al. (2006) Optimization of feline immunodeficiency virus vectors for RNA interference. J Virol 80:9371-80