Certain neurotransmitters act by binding to neuronal cell-surface receptors, changing intracellular levels of second messengers and the activities of their downstream effectors, and consequently altering the intrinsic properties of the neuron. This phenomenon, which is referred to as neuromodulation, is an important regulator of hippocampal pyramidal neuron function that is likely to have profound behavioral consequences. This proposal deals with investigating the molecular basis for neurotransmitter-induced neuromodulation in the hippocampus. One potentially rich site for mediating hippocampal neuromodulation is alteration of the biophysical and biochemical properties of potassium channels, as potassium channels play a major role in determining the electrical properties of hippocampal pyramidal neurons. One specific A- type potassium channel, Kv4.2, is located in the dendrites and cell bodies of pyramidal neurons in area CA1. This fact, coupled with the activation and inactivation properties of the channel, make this subtype of potassium channel ideally suited as a potential target for affecting short-term and long-term changes in the functional properties of pyramidal neurons. We are testing the hypothesis that one component of neurotransmitter-induced neuromodulation is mediated via phosphorylation of Kv4.2 We will do this by determining sites of phosphorylation of Kv4.2, directly determining if neurotransmitter application to hippocampal neurons leads to identified phosphorylation events, and dissecting the signal transduction cascades linking neurotransmitter receptors to Kv4.2 Interestingly, as part of our studies we will test the idea that the MAP kinase cascade is recruited by various neurotransmitters for modulation of Kv4.2 in the hippocampus. These studies, coupled with those described in the accompanying two proposals, should allow for the first time the definition of specific molecular events, of known physiologic consequence, as components of potassium channel-based neuromodulation in the hippocampus.

Project Start
1999-01-20
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Type
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Wang, Guangyu (2017) Mechanistic insight into the heme-independent interplay between iron and carbon monoxide in CFTR and Slo1 BKCa channels. Metallomics 9:634-645
Prince, Alison; Pfaffinger, Paul J (2013) Conserved N-terminal negative charges support optimally efficient N-type inactivation of Kv1 channels. PLoS One 8:e62695
Kunjilwar, Kumud; Qian, Yan; Pfaffinger, Paul J (2013) Functional stoichiometry underlying KChIP regulation of Kv4.2 functional expression. J Neurochem 126:462-72
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Nadin, Brian M; Pfaffinger, Paul J (2010) Dipeptidyl peptidase-like protein 6 is required for normal electrophysiological properties of cerebellar granule cells. J Neurosci 30:8551-65
Narayanan, Rishikesh; Dougherty, Kevin J; Johnston, Daniel (2010) Calcium store depletion induces persistent perisomatic increases in the functional density of h channels in hippocampal pyramidal neurons. Neuron 68:921-35
Dembrow, Nikolai C; Chitwood, Raymond A; Johnston, Daniel (2010) Projection-specific neuromodulation of medial prefrontal cortex neurons. J Neurosci 30:16922-37
Narayanan, Rishikesh; Johnston, Daniel (2010) The h current is a candidate mechanism for regulating the sliding modification threshold in a BCM-like synaptic learning rule. J Neurophysiol 104:1020-33
Prince-Carter, Alison; Pfaffinger, Paul J (2009) Multiple intermediate states precede pore block during N-type inactivation of a voltage-gated potassium channel. J Gen Physiol 134:15-34

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