Ca2+-induced Ca2+ release is a general mechanism that most cells use to amp
lify Ca2+ signals(1-5). In heart cells, this mechanism is operated between
voltage-gated L-type Ca2+ channels (LCCs) in the plasma membrane and Ca2+ r
elease channels, commonly known as ryanodine receptors, in the sarcoplasmic
reticulum(3-5) The Ca2+ influx through LCCs traverses a deft of roughly 12
nm formed by the cell surface and the sarcoplasmic reticulum membrane, and
activates adjacent ryanodine receptors to release Ca2+ in the form of Ca2 sparks(6). Here we determine the kinetics, fidelity and stoichiometry of c
oupling between LCCs and ryanodine receptors. We show that the local Ca2+ s
ignal produced by a single opening of an LCC named a 'Ca2+ sparklet: can tr
igger about 4-6 ryanodine receptors to generate a Ca2+ spark. The coupling
between LCCs and ryanodine receptors is stochastic, as judged by the expone
ntial distribution of the coupling latency. The fraction of sparklets that
successfully triggers a spark is less than unity and declines in a use-depe
ndent manner. This optical analysis of single-channel communication affords
a powerful means for elucidating Ca2+-signalling mechanisms at the molecul
ar level.