Sarkisov Dmitry V, Wang Samuel S-H
Department of Molecular Biology and Princeton Neuroscience Institute, Princeton University, Princeton, New Jersey 08544, USA.
J Neurosci. 2008 Jan 2;28(1):133-42. doi: 10.1523/JNEUROSCI.1729-07.2008.
Associative long-term depression (LTD) at cerebellar parallel fiber-Purkinje cell synapses is sensitive to the temporal order in which the parallel fiber is coactivated with the climbing fiber input, but how order sensitivity is achieved is unknown. Here we show that the cerebellar inositol-1,4,5-trisphosphate (IP3) receptor, whose activation is required for LTD induction, is sensitive in situ to the order of presentation of its coagonists, IP3 and cytoplasmic calcium. By focally photolyzing a novel caged IP3 compound in dendritic spines, we find that pairing IP3 with climbing fiber-mediated calcium entry leads to a large calcium release transient if the climbing fiber is activated up to 100 ms before or up to 500 ms after IP3 uncaging. This asymmetric timing window for coactivation follows the kinetics of calcium removal and IP3 unbinding from the receptor and is not limited by IP3 metabolism. IP3 receptor binding thus acts as an eligibility trace that can drive temporal order-dependent calcium release and LTD induction in Purkinje cells and event order-dependent sensory plasticity in the whole animal.
小脑平行纤维-浦肯野细胞突触处的联合性长时程抑制(LTD)对平行纤维与攀缘纤维输入共同激活的时间顺序敏感,但实现顺序敏感性的机制尚不清楚。在这里,我们表明,小脑肌醇-1,4,5-三磷酸(IP3)受体(其激活是LTD诱导所必需的)在原位对其协同激动剂IP3和细胞质钙的呈现顺序敏感。通过在树突棘中局部光解一种新型的笼状IP3化合物,我们发现,如果在IP3解笼前100毫秒或解笼后500毫秒内激活攀缘纤维,将IP3与攀缘纤维介导的钙内流配对会导致大量钙释放瞬变。这种共同激活的不对称时间窗口遵循钙清除和IP3从受体上解离的动力学,并且不受IP3代谢的限制。因此,IP3受体结合充当一种合格痕迹,可驱动浦肯野细胞中依赖时间顺序的钙释放和LTD诱导,以及全动物中依赖事件顺序的感觉可塑性。