How the brain develops from a proliferating progenitor pool into the most intricate structure in the human body is a fundamental question in 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. Specifically, these studies will explore the role of NF-kB signaling during telencephalic development. The NF-kB pathway has been intensively studied primarily in the context of the immune system where it plays a central role during development and in the adult. While some studies suggest a role for NF-kB in mature neurons, currently almost nothing is known about the role of this pathway in the embryonic forebrain. However, recent evidence suggests that this pathway is activated throughout telencephalic development and thus is likely to influence that process. This activation is particularly strong in the proliferative zone, supporting a role for NF-kB signaling in that region. Therefore, we will examine the effects of activating or blocking NF-kB in telencephalic progenitors on cell survival, proliferation, and fate both in vivo and in vitro. In particular we will use viral vectors for gene delivery, ultrasound-guided in utero surgery for in vivo studies, and both attached and neurosphere cultures for in vitro studies. These efforts will test the hypothesis that the predominant role of NF-kB signaling in the telencephalic proliferative zone is to promote the survival and maintenance of the progenitor pool. The studies will also consider potential interactions between the NF-kB, Notch, and FGF signaling pathways during telencephalic development. Numerous studies have suggested that these pathways can interact in the immune system and elsewhere, although the exact nature of those interactions remains unclear. Based upon the exploratory nature of this work we are requesting R21 level funding. The identification of NF-kB as relevant for mammalian forebrain development would be an important step in understanding this fundamental process. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21MH073006-02
Application #
7230207
Study Section
Neurogenesis and Cell Fate Study Section (NCF)
Program Officer
Panchision, David M
Project Start
2006-04-01
Project End
2008-03-31
Budget Start
2007-04-01
Budget End
2008-03-31
Support Year
2
Fiscal Year
2007
Total Cost
$214,816
Indirect Cost
Name
Johns Hopkins University
Department
Neurology
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Yamanishi, Emiko; Yoon, Keejung; Alberi, Lavinia et al. (2015) NF-?B signaling regulates the generation of intermediate progenitors in the developing neocortex. Genes Cells 20:706-19