The role that a neuron plays in a neural network is shaped by its intrinsic excitability, which is established developmentally to co-ordinate with its function within that network. We will study the control of neuronal firing properties in the rat peripheral sympathetic nervous system. There are two types of neurons in this system. Neurons in paravertebral ganglia have a simple wiring diagram and synaptic input to these cells is dominated by a large suprathreshold input from a single preganglionic motor neuron. These cells strongly accommodate in response to a sustained depolarizing current and are known as phasic neurons. In contrast, neurons in prevertebral ganglia integrate multiple small synaptic inputs from both sensory and motor neurons. These cells fire repetitively in response to a sustained depolarizing current and are known as tonic neurons. These different firing properties are determined by the differential expression of specific potassium currents. Phasic firing is produced by expression of a relatively large M-current. Tonic firing properties correlate with expression of an inward rectifier current and a low threshold, slowly inactivating current known as a D2 current. These two distinct electrophysiological phenotypes are determined during development by inductive events that affect transcriptional regulation of potassium channel genes. The overall aim of this proposal is to determine the molecular identity of those currents that control the switch in firing properties and to understand how the regulation of these channels is achieved. This work has relevance to the study of epilepsy since the regulation of intrinsic neuronal excitability is a key factor in determining the overall excitability of a neural network.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS029755-10
Application #
6639431
Study Section
Integrative, Functional and Cognitive Neuroscience 8 (IFCN)
Program Officer
Stewart, Randall
Project Start
1992-07-01
Project End
2005-03-31
Budget Start
2003-04-01
Budget End
2004-03-31
Support Year
10
Fiscal Year
2003
Total Cost
$338,625
Indirect Cost
Name
State University New York Stony Brook
Department
Other Basic Sciences
Type
Schools of Arts and Sciences
DUNS #
804878247
City
Stony Brook
State
NY
Country
United States
Zip Code
11794
Rosati, Barbara; McKinnon, David (2009) Structural and regulatory evolution of cellular electrophysiological systems. Evol Dev 11:610-8
Rosati, Barbara; Dong, Min; Cheng, Lan et al. (2008) Evolution of ventricular myocyte electrophysiology. Physiol Genomics 35:262-72
Rosati, Barbara; Dun, Wen; Hirose, Masanori et al. (2007) Molecular basis of the T- and L-type Ca2+ currents in canine Purkinje fibres. J Physiol 579:465-71
Rosati, Barbara; Grau, Frederic; McKinnon, David (2006) Regional variation in mRNA transcript abundance within the ventricular wall. J Mol Cell Cardiol 40:295-302
Rosati, Barbara; Grau, Frederic; Kuehler, Anneke et al. (2004) Comparison of different probe-level analysis techniques for oligonucleotide microarrays. Biotechniques 36:316-22
Rosati, Barbara; McKinnon, David (2004) Regulation of ion channel expression. Circ Res 94:874-83
Rosati, Barbara; Grau, Frederic; Rodriguez, Samantha et al. (2003) Concordant expression of KChIP2 mRNA, protein and transient outward current throughout the canine ventricle. J Physiol 548:815-22
Pan, Z; Selyanko, A A; Hadley, J K et al. (2001) Alternative splicing of KCNQ2 potassium channel transcripts contributes to the functional diversity of M-currents. J Physiol 531:347-58
Rosati, B; Pan, Z; Lypen, S et al. (2001) Regulation of KChIP2 potassium channel beta subunit gene expression underlies the gradient of transient outward current in canine and human ventricle. J Physiol 533:119-25
Wang, H S; Brown, B S; McKinnon, D et al. (2000) Molecular basis for differential sensitivity of KCNQ and I(Ks) channels to the cognitive enhancer XE991. Mol Pharmacol 57:1218-23

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