During the past decade our understanding of the dynamic integrative capacity of astrocytes, a sub-type of glial cell of the CNS, has dramatically increased. While once thought to play only supportive roles, recent data suggest that neuronal activity raises astrocytic calcium levels, which in turn cause a feedback release of chemical transmitter from astrocytes to modulate neighboring neurons. We will use acutely isolated hippocampal slice preparations to test the hypothesis that calcium elevations in astrocytes cause neuromodulatory functions resulting from the calcium-dependent release of glutamate from astrocytes. To achieve this experimental objective we will perform integrated studies in which we monitor internal calcium using confocal microscopy, manipulate astrocytic calcium levels using focal flash photolysis of caged compounds, and record synaptic transmission using patch clamp recordings. In order to unambiguously identify astrocytes, we will use transgenic mice in which green fluorescent protein (GFP) is expressed selectively in astrocytes. We will determine whether: 1) hippocampal astrocytes exhibit functional compartmentalization of calcium signaling within their processes; 2) waves of elevated calcium can propagate between astrocytes in hippocampal slices; 3) the calcium-dependent release of neurotransmitters from astrocytes regulates internal calcium levels and the excitability of neighboring neurons and astrocytes; 4) the calcium-dependent release of glutamate from astrocytes dynamically controls synaptic transmission. By performing these studies we will obtain new insights into the roles of astrocytes in integration in the CNS. Since astrocytes can integrate neuronal inputs and can release glutamate in response to elevated internal calcium, the demonstration of a neuromodulatory capacity for astrocytes has the potential to significantly change the way we view computation in the nervous system.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS043142-05
Application #
6916326
Study Section
Special Emphasis Panel (ZRG1-SSS-Q (01))
Program Officer
Fountain, Jane W
Project Start
2001-07-15
Project End
2006-06-30
Budget Start
2005-07-01
Budget End
2006-06-30
Support Year
5
Fiscal Year
2005
Total Cost
$391,067
Indirect Cost
Name
University of Pennsylvania
Department
Neurosciences
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Carmignoto, Giorgio; Haydon, Philip G (2012) Astrocyte calcium signaling and epilepsy. Glia 60:1227-33
Florian, Cédrick; Vecsey, Christopher G; Halassa, Michael M et al. (2011) Astrocyte-derived adenosine and A1 receptor activity contribute to sleep loss-induced deficits in hippocampal synaptic plasticity and memory in mice. J Neurosci 31:6956-62
Lee, So-Young; Haydon, Philip G (2011) A cytokine-dependent switch for glial-neuron interactions. Neuron 69:835-7
Dong, Jinghui; Revilla-Sanchez, Raquel; Moss, Stephen et al. (2010) Multiphoton in vivo imaging of amyloid in animal models of Alzheimer's disease. Neuropharmacology 59:268-75
Halassa, Michael M; Haydon, Philip G (2010) Integrated brain circuits: astrocytic networks modulate neuronal activity and behavior. Annu Rev Physiol 72:335-55
Potokar, Maja; Kreft, Marko; Lee, So-Young et al. (2009) Trafficking of astrocytic vesicles in hippocampal slices. Biochem Biophys Res Commun 390:1192-6
Halassa, Michael M; Fellin, Tommaso; Haydon, Philip G (2009) Tripartite synapses: roles for astrocytic purines in the control of synaptic physiology and behavior. Neuropharmacology 57:343-6
Haydon, Philip G; Blendy, Julie; Moss, Stephen J et al. (2009) Astrocytic control of synaptic transmission and plasticity: a target for drugs of abuse? Neuropharmacology 56 Suppl 1:83-90
Halassa, Michael M; Florian, Cedrick; Fellin, Tommaso et al. (2009) Astrocytic modulation of sleep homeostasis and cognitive consequences of sleep loss. Neuron 61:213-9
D'Ascenzo, Marcello; Fellin, Tommaso; Terunuma, Miho et al. (2007) mGluR5 stimulates gliotransmission in the nucleus accumbens. Proc Natl Acad Sci U S A 104:1995-2000

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