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Calcium dependence of the rate of exocytosis in a synaptic terminal

MPG-Autoren
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Heidelberger,  R.
Department of Membrane Biophysics, MPI for biophysical chemistry, Max Planck Society;

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Heinemann,  C.
Department of Membrane Biophysics, MPI for biophysical chemistry, Max Planck Society;

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Neher,  E.
Department of Membrane Biophysics, MPI for biophysical chemistry, Max Planck Society;

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Zitation

Heidelberger, R., Heinemann, C., Neher, E., & Matthews, G. (1994). Calcium dependence of the rate of exocytosis in a synaptic terminal. Nature, 371(6497), 513-515. doi:10.1038/371513a0.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-0013-045F-A
Zusammenfassung
RAPID calcium-dependent exocytosis underlies neurotransmitter release from nerve terminals. Despite the fundamental importance of this process, neither the relationship between presynaptic intra-cellular calcium ion concentration ([Ca2+]i) and rate of exocytosis, nor the maximal rate of secretion is known quantitatively. To provide this information, we have used flash photolysis of caged Ca2+ to elevate [Ca2+]i rapidly and uniformly in synaptic terminals, while measuring membrane capacitance as an index of exocytosis and monitoring [Ca2+]i with a Ca2+-indicator dye. When [Ca2+]i was abruptly increased to >10 µM, capacitance rose at a rate that increased steeply with [Ca2+]i. The steepness suggested that at least four calcium ions must bind to activate synaptic vesicle fusion. Half-saturation was at 194 µM, and the maximal rate constant was 2,000–3,000 s–1. A given synaptic vesicle can exocytose with high probability within a few hundred microseconds, if [Ca2+]i rises above lOOµM. These properties provide for the extremely rapid signalling required for neuronal communication.