How the mammalian brain develops from a proliferating progenitor pool into the most intricate structure in the body is a fundamental question facing modern biology. The work proposed here investigates this question in the telencephalon, the embryonic structure that gives rise to the cerebral cortex and other areas of higher brain function. In addition, these studies will consider the relationship between embryonic neural progenitors and those present in the postnatal brain. Our specific objectives are to understand in depth how the Notch and FGF signaling pathways influence telencephalic progenitors. Previous studies have shown that these pathways play critical roles during progenitor maintenance, proliferation, and differentiation. A defining feature of our approach is an emphasis on characterizing progenitors in vivo. Using our uniquely powerful gain-of-function system, we will genetically modify neural progenitors in the mouse embryo in utero, and examine the fate of those cells during development and in the adult. By combining this approach with in vitro proliferation and developmental potential assays, we will gain insight into the endogenous mechanisms regulating neural progenitors. These studies will also seek to determine specifically which receptors and downstream effectors mediate the effects of Notch signaling in telencephalic progenitors. This work will be complemented by loss-of-function studies focused on understanding the effects of deleting Notch and FGF receptors in telencephalic progenitors. Furthermore, using a novel transgenic approach we will prospectively isolate and characterize telencephalic progenitors containing endogenous Notch activation. By advancing an understanding of the basic mechanisms that regulate mammalian neural progenitors we hope to uncover fundamental principles with potential medical utility. In particular, these studies are likely to facilitate the manipulation of stem cells for therapeutic use in the nervous system and elsewhere.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS046731-04
Application #
7261388
Study Section
Neurogenesis and Cell Fate Study Section (NCF)
Program Officer
Owens, David F
Project Start
2004-09-15
Project End
2009-05-31
Budget Start
2007-06-01
Budget End
2008-05-31
Support Year
4
Fiscal Year
2007
Total Cost
$358,502
Indirect Cost
Name
Johns Hopkins University
Department
Neurology
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Liu, Shuxi; Wang, Yue; Worley, Paul F et al. (2015) The canonical Notch pathway effector RBP-J regulates neuronal plasticity and expression of GABA transporters in hippocampal networks. Hippocampus 25:670-8
Pierfelice, Tarran J; Schreck, Karisa C; Dang, Louis et al. (2011) Notch3 activation promotes invasive glioma formation in a tissue site-specific manner. Cancer Res 71:1115-25
Ever, Leah; Zhao, Rui-Jing; Eswarakumar, Veraragavan P et al. (2008) Fibroblast growth factor receptor 2 plays an essential role in telencephalic progenitors. Dev Neurosci 30:306-18
Dang, Louis; Yoon, Keejung; Wang, Mike et al. (2006) Notch3 signaling promotes radial glial/progenitor character in the mammalian telencephalon. Dev Neurosci 28:58-69