Fujiwara A, Hirose K, Yamazawa T, Iino M
Department of Pharmacology, Graduate School of Medicine, The University of Tokyo, Japan.
Neuroreport. 2001 Aug 28;12(12):2647-51. doi: 10.1097/00001756-200108280-00012.
The inositol 1,4,5-trisphosphate receptor (IP3R) is highly expressed in Purkinje neurons (PNs) and is thought to be essential for the induction of long-term depression at parallel-fiber-PN synapses. Here, by imaging the fluorescence 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+ release is dependent on the IP3 concentration with an EC50 of 25.8 microM, 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 release of Ca2+ in a localized space adjacent to the site of synaptic inputs.
肌醇1,4,5-三磷酸受体(IP3R)在浦肯野神经元(PNs)中高度表达,并且被认为对于平行纤维-PN突触处的长时程抑制的诱导至关重要。在此,通过对通透的单个PNs中钙库内低亲和力Ca2+指示剂的荧光强度进行成像,我们在可控的细胞质环境中分析了经由IP3R的Ca2+释放动力学。Ca2+释放速率取决于IP3浓度,其半数有效浓度(EC50)为25.8微摩尔,这比在分离制剂或外周细胞中的IP3R的该值大20倍以上。这种特性在诱导与突触输入位点相邻的局部空间中的Ca2+释放方面将是有利的。