The inositol 1,4,S-trisphosphate receptor (IP3R) is highly expressed in Pur
kinje neurons (PNs) and is thought to be essential for the induction of lon
g-term depression at parallel-fiber-PN synapses. Here, by imaging the fluor
escence intensity of the low-affinity Ca2+ indicator inside the Ca2+ stores
in the permeabilized single PNs, we analyzed the kinetics of Ca2+ release
via the IP3R in controlled cytoplasmic environments. The rate of Ca2+ relea
se is dependent on the IP3 concentration with an EC50 of 25.8 muM, which is
> 20-fold greater than that of the IP3R in the isolated preparations or in
peripheral cells. This property would be advantageous in inducing the rele
ase of Ca2+ in a localized space adjacent to the site of synaptic inputs. N
euroReport 12:2647-2651 (C) 2001 Lippincott Williams & Wilkins.