The postnatal subventricular zone (SVZ) is a germinal zone containing distinct immature cell types, including stem cells and migrating neuronal progenitors. Understanding the in situ physiological properties of SVZ cells and the diffusible factors influencing SVZ cell physiology is critical to allow endogenous activation of stem cells/progenitors and induction of self-repair. In situ SVZ cell physiology and SVZ signaling factors are, however, largely unknown. Because the identity of neural stem cells is still debated, we propose to identify the signaling factors that regulate SVZ cell properties and could in particular influence neuronal progenitor migration. GABA is a likely candidate as a signaling factor because it regulates migration of embryonic cells and its synthetic enzyme is present in the SVZ. We thus hypothesize that GABA is a signaling factor locally released by migrating progenitors at rest resulting in activation of GABA autoreceptors and ion channels known to be involved in cell migration. The two following aims will be addressed with whole-cell and perforated patch-clamp recordings, and with fluorimetric Ca2+ measurements in SVZ slices.
The first aim will determine whether GABA activates GABA receptors (GABAR5) on neuronal progenitors and whether GABAR activation leads to Ca2+ increase and Ca2+-dependent K+ (KCa) channel activation, which triggers membrane potential changes. KCa channel activation is known to be a prerequisite for migration of other cell types.
The second aim will investigate whether GABARs are activated by transport-mediated GABA efflux from progenitors following membrane potential depolarization. Neuronal progenitors will be recorded from transgenic mice expressing yellow fluorescent protein in such progenitors under the control of the tubulin promoter. Data from these studies will provide the first fundamental insight into the physiology of SVZ cells in situ and exposes a novel concept of cell migration governed by an interplay between GABARs and GABA transporters.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21NS044161-01
Application #
6513647
Study Section
Molecular, Cellular and Developmental Neurosciences 2 (MDCN)
Program Officer
Chiu, Arlene Y
Project Start
2002-07-01
Project End
2004-05-31
Budget Start
2002-07-01
Budget End
2003-05-31
Support Year
1
Fiscal Year
2002
Total Cost
$151,758
Indirect Cost
Name
Yale University
Department
Neurosurgery
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
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Bolteus, Anna J; Bordey, Angelique (2004) GABA release and uptake regulate neuronal precursor migration in the postnatal subventricular zone. J Neurosci 24:7623-31
Wang, D D; Krueger, D D; Bordey, A (2003) GABA depolarizes neuronal progenitors of the postnatal subventricular zone via GABAA receptor activation. J Physiol 550:785-800
Wang, D D; Krueger, D D; Bordey, A (2003) Biophysical properties and ionic signature of neuronal progenitors of the postnatal subventricular zone in situ. J Neurophysiol 90:2291-302