The process of neuronal integration takes place at the cell body and initial axon segment of the neuron where synaptic input is received and processed. One important influence on the processing of information is the character of the excitable membrane in this region of the cell. We are using voltage clamp and sensitive new method for recording current from a restricted area of membrane to map the spatial distribution of different types of ion channels across the cell surface. The goal of this project is to determine how the regional specialization of function in the neuron comes about and how a heterogeneous distribution of ion channels can be maintained. The excitability of nerve cells can be modified by various peptide hormones, but the mechanism of this important effect is not well understood. We are investigating the final steps in hormonal modulation by studying peptide effects on ionic currents in neurons of the molluscs Helix and Aplysia. We are asking where on the cell the hormone acts, which currents are modified and how. Of particular interest to us are the ionic currents that are active near the resting potential since these provide the background ionic conductance upon which neuronal integration works. Using voltage clamp methods we are studying the ionic currents near the resting potential to find the mechanism of post-inhibitory rebound and to determine if the Ca-dependent current is activated in the resting cell. Membrane ionic currents are important to the regulation of cellular activity in many types of cells, and in some cases non-neuronal cells provide excellent models for studying these regulatory events. One example is the lymphocytes of the immune system. Using membrane-patch voltage clamp, the role of the cell membrane in antigen-dependent lymphocyte activation, cell differentiation and effector cell function can be studied. We are using a cloned T-cell line that provides a particularly good preparation for study of the regulation of ion channels. Another project involves study of voltage-dependent potassium channels in the nerve cell body to further define its role in repetitive firing.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS014519-08
Application #
3395609
Study Section
Physiology Study Section (PHY)
Project Start
1978-07-01
Project End
1987-03-31
Budget Start
1986-04-01
Budget End
1987-03-31
Support Year
8
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
Schools of Arts and Sciences
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Mathes, C; Thompson, S H (1996) The nitric oxide/cGMP pathway couples muscarinic receptors to the activation of Ca2+ influx. J Neurosci 16:1702-9
Wang, S S; Alousi, A A; Thompson, S H (1995) The lifetime of inositol 1,4,5-trisphosphate in single cells. J Gen Physiol 105:149-71
Coggan, J S; Thompson, S H (1995) Intracellular calcium signals in response to bradykinin in individual neuroblastoma cells. Am J Physiol 269:C841-8
Thompson, S H; Mathes, C; Alousi, A A (1995) Calcium requirement for cGMP production during muscarinic activation of N1E-115 neuroblastoma cells. Am J Physiol 269:C979-85
Mathes, C; Thompson, S H (1995) The relationship between depletion of intracellular Ca2+ stores and activation of Ca2+ current by muscarinic receptors in neuroblastoma cells. J Gen Physiol 106:975-93
Wang, S S; Thompson, S H (1995) Local positive feedback by calcium in the propagation of intracellular calcium waves. Biophys J 69:1683-97
Coggan, J S; Kovacs, I; Thompson, S H (1994) The aminoglycoside G418 suppresses muscarinic receptor-activated calcium release in stably transfected murine N1E-115 neuroblastoma cells. Neurosci Lett 170:247-50
Mathes, C; Thompson, S H (1994) Calcium current activated by muscarinic receptors and thapsigargin in neuronal cells. J Gen Physiol 104:107-21
Wang, S S; Thompson, S H (1994) Measurement of changes in functional muscarinic acetylcholine receptor density in single neuroblastoma cells using calcium release kinetics. Cell Calcium 15:483-96
Wang, S S; Mathes, C; Thompson, S H (1993) Membrane toxicity of the protein kinase C inhibitor calphostin A by a free-radical mechanism. Neurosci Lett 156:145-8

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