The main goal of this project is to study the regulation of nicotinic acetylcholine receptors (nAChRs) in the CNS by neuregulins, a new family of neurotrophic factors that are present in cholinergic neurons throughout central and peripheral nervous system. We will also determine if neuregulin induced change in the number of distribution of functional nAChRs alters synaptic transmission in the circuits described. Neuregulins will be studied in vitro by adding them to neuronal cell cultures, and they will be studied in vivo in mutant mice that exhibit diminished neuregulin expression. To maximize the generality of our results, we will study neurons dissociated from the Medial Habenula (MHb), the Interpeduncular Nucleus (IPN), the Substantia Nigra, (SN), and the Ventral Tegmental Area (VTA). Each region offers advantages for studies of nAChR regulation. In each case, the nuclei can be dissected easily from embryos and neonatal animals, the cells can be maintained in spars cell culture, a subpopulation of the neurons receive cholinergic synaptic inputs, and the neurons express a diverse array of nAChRs. In vitro cell culture experiments are described in the three Specific Aims. In vivo studies that utilize fresh slices prepared from normal and mutant mice are described in Collaborations. We emphasize microelectrode recordings of ACh induced currents because we want to study regulation of functional receptors. However, ligand binding and receptor subunit gene expression will be used to confirm and extend results in some cases. In each series of experiments, we will begin with the relatively well studied MHb-IPN system, but results will be extended to Septal-MHb, and PPT-SN/VTA interactions.

Project Start
2001-12-01
Project End
2002-11-30
Budget Start
Budget End
Support Year
4
Fiscal Year
2002
Total Cost
$295,873
Indirect Cost
Name
Harvard University
Department
Type
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
Richards, Kathryn S; Swensen, Andrew M; Lipscombe, Diane et al. (2007) Novel CaV2.1 clone replicates many properties of Purkinje cell CaV2.1 current. Eur J Neurosci 26:2950-61
McDonough, Stefan I; Mori, Yasuo; Bean, Bruce P (2005) FPL 64176 modification of Ca(V)1.2 L-type calcium channels: dissociation of effects on ionic current and gating current. Biophys J 88:211-23
Martina, Marco; Yao, Gui Lan; Bean, Bruce P (2003) Properties and functional role of voltage-dependent potassium channels in dendrites of rat cerebellar Purkinje neurons. J Neurosci 23:5698-707
Swensen, Andrew M; Bean, Bruce P (2003) Ionic mechanisms of burst firing in dissociated Purkinje neurons. J Neurosci 23:9650-63
Blitz, Dawn M; Regehr, Wade G (2003) Retinogeniculate synaptic properties controlling spike number and timing in relay neurons. J Neurophysiol 90:2438-50
Blair, Nathaniel T; Bean, Bruce P (2003) Role of tetrodotoxin-resistant Na+ current slow inactivation in adaptation of action potential firing in small-diameter dorsal root ganglion neurons. J Neurosci 23:10338-50
Do, Michael Tri H; Bean, Bruce P (2003) Subthreshold sodium currents and pacemaking of subthalamic neurons: modulation by slow inactivation. Neuron 39:109-20
Mitterdorfer, Jorg; Bean, Bruce P (2002) Potassium currents during the action potential of hippocampal CA3 neurons. J Neurosci 22:10106-15
Blair, Nathaniel T; Bean, Bruce P (2002) Roles of tetrodotoxin (TTX)-sensitive Na+ current, TTX-resistant Na+ current, and Ca2+ current in the action potentials of nociceptive sensory neurons. J Neurosci 22:10277-90
Chen, Chinfei; Blitz, Dawn M; Regehr, Wade G (2002) Contributions of receptor desensitization and saturation to plasticity at the retinogeniculate synapse. Neuron 33:779-88

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