(from the application): The molecular mechanisms governing the decision of dividing neural progenitor cells to exit the cell cycle and differentiate into mature nondividing cells, such as neurons and oligodendrocytes, are incompletely understood. Shortening of the specialized ends of chromosomes, called telomeres, has been proposed as a means used by cells to monitor and limit their number of cell divisions. The ribonucleoprotein DNA polymerase telomerase is important for maintenance of telomeric length and integrity. Differentiation of several immortalized cell lines, including leukemic cells, teratocarcinoma, and pheochromocytorna cells, is associated with loss of telomerase activity and shortening of telomeres. It is not known how telomerase activity, regulation of telomere length, and differentiation are coupled, but DNA checkpoint control and activation of cellcycle suppressor molecules have been implicated. The role of telomeres and telomerase in the proliferation and differentiation of progenitor cells in the brain will be examined. The levels of telomerase in primary cultures of neural progenitor cells before and after differentiation will be investigated by activity assays, immunoblotting, and microscopy. Subsequent studies will employ biochemical methods to examine telomere length and shortening and the regulation of telomerase levels. Transgenic mice and protein transduction experiments will attempt to demonstrate a causal role for telomerase in neural proliferation and differentiation. In addition to contributing to an understanding of the regulatory mechanisms of neurogenesis and gliogenesis in the mammalian brain, such studies would be useful in exploring the ability of the brain to replace cells lost during aging, neurodegenerative diseases. and stroke and in designing therapies to treat these maladies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Clinical Investigator Award (CIA) (K08)
Project #
7K08NS002249-05
Application #
6895402
Study Section
National Institute of Neurological Disorders and Stroke Initial Review Group (NSD)
Program Officer
Tagle, Danilo A
Project Start
2000-09-30
Project End
2005-08-31
Budget Start
2004-07-01
Budget End
2004-08-31
Support Year
5
Fiscal Year
2003
Total Cost
$12,647
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Neurology
Type
Schools of Medicine
DUNS #
060217502
City
New York
State
NY
Country
United States
Zip Code
10065
Taveggia, Carla; Thaker, Pratik; Petrylak, Ashley et al. (2008) Type III neuregulin-1 promotes oligodendrocyte myelination. Glia 56:284-93
Caporaso, Gregg L; Lim, Daniel A; Alvarez-Buylla, Arturo et al. (2003) Telomerase activity in the subventricular zone of adult mice. Mol Cell Neurosci 23:693-702
Caporaso, G L; Chao, M V (2001) Telomerase and oligodendrocyte differentiation. J Neurobiol 49:224-34