Olfactory bulb (OB) ablations induce massive cell death among olfactory neurons (ORNs) and an expansion of the population of mitotic basal cells (BC). Within a week after bulbectomy new neurons are generated. As the ORN population grows, the number of mitotic BC decrease. To determine the mechanism for the regulation of OE regeneration, I am using microarray technology to analyze the dynamics of gene expression in OE from bulbectomized mice. I am in the process of performing several time-course studies to identify genes that are tightly correlated with regeneration. OE cRNA from bulbectomized mice are being used to probe an Affymetrix mouse gene chip. Genes found to be tightly correlated with the regenerating OE will be further analyzed for expression patterns. Once an expression pattern is identified to be appropriate for a potential role in regeneration, gene function will be perturbed using commercial reagents and/or retrovirus in in vivo experimental paradigms. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31DC006200-01
Application #
6649100
Study Section
Communication Disorders Review Committee (CDRC)
Program Officer
Sklare, Dan
Project Start
2003-01-01
Project End
Budget Start
2003-01-01
Budget End
2003-12-31
Support Year
1
Fiscal Year
2003
Total Cost
$33,513
Indirect Cost
Name
Columbia University (N.Y.)
Department
Biology
Type
Other Domestic Higher Education
DUNS #
049179401
City
New York
State
NY
Country
United States
Zip Code
10027