Astrocytes are the most prevalent cell in brain and yet we know virtually nothing about the role of these cells in brain function or disorders. Results from in vitro studies strongly support the concept that the activity of astrocytes is coupled to neuronal activity through neurotransmitter signalling systems. However, no one has shown that astrocytes respond to neurotransmitters released during normal neuronal activity in vivo. The goal of this project is to determine the level of neuronal activity required to activate astrocytes in vivo. It is our premise that a large percentage of neurotransmitter release in vivo may be related to direct signalling between neurons and astrocytes. All available evidence from in vitro studies is consistent with the hypothesis that astrocytes form an extraneuronal signalling system in brain and that this system could profoundly influence the synaptic efficacy of neurons. The long-term goal of our studies is to determine if astrocytes influence neuronal communication in vivo. The vast majority of research on the pharmacology of astrocytes has focused on the responses of astroglia in culture. It is now essential to move beyond cell culture systems and into intact brain tissue to study neuronal-astrocytic interactions in the enormously complex geometry of brain. It is only in the intact brain that the proximity of neurotransmitter release sites, receptors, and inactivation systems remain physiological. It is only here that we can determine if astrocytes respond to neuronal activity and if so, what the function of that response might be. We have chosen to study neuronal-astrocytic communication in the stratum radiatum of CA1 hippocampus. Innervation of CA1 pyramidal neuron apical dendrites in this region occurs primarily through excitatory input from glutamatergic CA3 pyramidal neurons and local inhibitory input from GABAergic interneurons. Confocal microscopy will be used to examine neuronal and astrocytic calcium responses to basal- and stimulus evoked- neurotransmitter release in CA1 s. radiatum. Pharmacological agents will be used to determine whether astrocytic responses reflect neurotransmitter release from neuronal terminals or axons. Developmental studies will be carried out to determine if astrocytic responsiveness changes during brain maturation. The results of these experiments will determine the degree of communication between astrocytes and neurons, the two predominant cell types in brain.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS020212-14
Application #
2460499
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Program Officer
Baughman, Robert W
Project Start
1983-12-01
Project End
1999-07-31
Budget Start
1997-08-01
Budget End
1998-07-31
Support Year
14
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Pharmacology
Type
Schools of Medicine
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Khakh, Baljit S; McCarthy, Ken D (2015) Astrocyte calcium signaling: from observations to functions and the challenges therein. Cold Spring Harb Perspect Biol 7:a020404
Song, Yurong; Zhang, Qian; Kutlu, Burak et al. (2013) Evolutionary etiology of high-grade astrocytomas. Proc Natl Acad Sci U S A 110:17933-8
Agulhon, Cendra; Boyt, Kristen M; Xie, Alison Xiaoqiao et al. (2013) Modulation of the autonomic nervous system and behaviour by acute glial cell Gq protein-coupled receptor activation in vivo. J Physiol 591:5599-609
Agulhon, Cendra; Fiacco, Todd A; McCarthy, Ken D (2010) Hippocampal short- and long-term plasticity are not modulated by astrocyte Ca2+ signaling. Science 327:1250-4
Petravicz, Jeremy; Fiacco, Todd A; McCarthy, Ken D (2008) Loss of IP3 receptor-dependent Ca2+ increases in hippocampal astrocytes does not affect baseline CA1 pyramidal neuron synaptic activity. J Neurosci 28:4967-73
Agulhon, Cendra; Petravicz, Jeremy; McMullen, Allison B et al. (2008) What is the role of astrocyte calcium in neurophysiology? Neuron 59:932-46
Casper, Kristen B; McCarthy, Ken D (2006) GFAP-positive progenitor cells produce neurons and oligodendrocytes throughout the CNS. Mol Cell Neurosci 31:676-84
Howe, D G; McCarthy, K D (2000) Retroviral inhibition of cAMP-dependent protein kinase inhibits myelination but not Schwann cell mitosis stimulated by interaction with neurons. J Neurosci 20:3513-21
Shao, Y; McCarthy, K D (1997) Responses of Bergmann glia and granule neurons in situ to N-methyl-D-aspartate, norepinephrine, and high potassium. J Neurochem 68:2405-11
Porter, J T; McCarthy, K D (1996) Hippocampal astrocytes in situ respond to glutamate released from synaptic terminals. J Neurosci 16:5073-81

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