1. Abteilung Membranbiophysik, Max-Planck-Institut für biophysikalische Chemie, Am Fassberg 11, D-37077 Göttingen , Germany

Correspondence to: Ralf Schneggenburger Correspondence and requests for materials should be addressed to R.S. (e-mail: Email: rschneg@gwdg.de).

Abstract

Calcium-triggered fusion of synaptic vesicles and neurotransmitter release are fundamental signalling steps in the central nervous system. It is generally assumed that fast transmitter release is triggered by elevations in intracellular calcium concentration ([Ca²⁺]_i) to at least 100 M near the sites of vesicle fusion^{1, 2, 3, 4, 5}. For synapses in the central nervous system, however, there are no experimental estimates of this local [Ca²⁺]_i signal. Here we show, by using calcium ion uncaging in the large synaptic terminals of the calyx of Held, that step-like elevations to only 10 M [Ca²⁺] _i induce fast transmitter release, which depletes around 80% of a pool of available vesicles in less than 3 ms. Kinetic analysis of transmitter release rates after [Ca²⁺]_i steps revealed the rate constants for calcium binding and vesicle fusion. These show that transient (around 0.5 ms) local elevations of [Ca²⁺]_i to peak values as low as 25 M can account for transmitter release during single presynaptic action potentials. The calcium sensors for vesicle fusion are far from saturation at normal release probability. This non-saturation, and the high intracellular calcium cooperativity in triggering vesicle fusion, make fast synaptic transmission very sensitive to modulation by changes in local [Ca²⁺]_i.

1. Abteilung Membranbiophysik, Max-Planck-Institut für biophysikalische Chemie, Am Fassberg 11, D-37077 Göttingen , Germany

Correspondence to: Ralf Schneggenburger Correspondence and requests for materials should be addressed to R.S. (e-mail: Email: rschneg@gwdg.de).