The overall aim of this project is to describe the mechanism by which the properties of ion channels in the membranes of excitable cells can be modulated by events occurring within the intracellular environment, in both developing and adult cells. The specific experiments of this proposal will be done on starfish oocytes. Immature oocytes are large, amenable to a variety of detailed electrophysiological techniques, and under voltage-clamp display voltage-dependent Ca and K currents similar or those of adult neurons and muscle fibers. My preliminary studies have shown that the properties of both Ca and K currents change dramatically during maturation of the oocytes, the final (1-2 hr.) step of oogenesis during which meiosis is reinitiated and the oocyte becomes fertilizable. These changes in the active electrical properties of the oocyte are required for normal fertilization of the mature egg to occur. Although this preparation provides an ideal opportunity to examine rigorously the mechanisms by which Ca and K channel properties are modified during early development, no previous studies have investigated these mechanisms. I will use voltage-clamp, patch-clamp, and ion--sensitive microelectrode techniques to study the effects of maturation and fertilization on Ca and K channel properties. The goal of these experiments is to understand the cellular events of early development which cause the changes in ion channel properties. The results obtained will be of relevance to pathologies affecting the fertilization process, the early development of the nervous system, and the electrical properties of adult nerve and muscle.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD017486-03
Application #
3314493
Study Section
Physiology Study Section (PHY)
Project Start
1983-04-01
Project End
1986-03-31
Budget Start
1985-04-01
Budget End
1986-03-31
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
Schools of Arts and Sciences
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Davidson, Brad; Swalla, Billie J (2002) A molecular analysis of ascidian metamorphosis reveals activation of an innate immune response. Development 129:4739-51
Dallman, J E; Dorman, J B; Moody, W J (2000) Action potential waveform voltage clamp shows significance of different Ca2+ channel types in developing ascidian muscle. J Physiol 524 Pt 2:375-86
Moody, W J (1998) The development of voltage-gated ion channels and its relation to activity-dependent development events. Curr Top Dev Biol 39:159-85
Dallman, J E; Davis, A K; Moody, W J (1998) Spontaneous activity regulates calcium-dependent K+ current expression in developing ascidian muscle. J Physiol 511 ( Pt 3):683-93
Greaves, A A; Davis, A K; Dallman, J E et al. (1996) Co-ordinated modulation of Ca2+ and K+ currents during ascidian muscle development. J Physiol 497 ( Pt 1):39-52
Davis, A K; Greaves, A A; Dallman, J E et al. (1995) Comparison of ionic currents expressed in immature and mature muscle cells of an ascidian larva. J Neurosci 15:4875-84
Villaz, M; Cinniger, J C; Moody, W J (1995) A voltage-gated chloride channel in ascidian embryos modulated by both the cell cycle clock and cell volume. J Physiol 488 ( Pt 3):689-99
Linsdell, P; Moody, W J (1995) Electrical activity and calcium influx regulate ion channel development in embryonic Xenopus skeletal muscle. J Neurosci 15:4507-14
Linsdell, P; Moody, W J (1994) Na+ channel mis-expression accelerates K+ channel development in embryonic Xenopus laevis skeletal muscle. J Physiol 480 ( Pt 3):405-10
Nevitt, G A; Dittman, A H; Quinn, T P et al. (1994) Evidence for a peripheral olfactory memory in imprinted salmon. Proc Natl Acad Sci U S A 91:4288-92

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