Mori-Kawakami Fumiko, Kobayashi Katsunori, Takahashi Tomoyuki
Department of Neurophysiology, University of Tokyo Graduate School of Medicine, Tokyo 113-0033, Japan.
J Physiol. 2003 Nov 15;553(Pt 1):37-48. doi: 10.1113/jphysiol.2003.045948. Epub 2003 Sep 8.
Transmission at the hippocampal mossy fibre (MF)-CA3 pyramidal cell synapse is characterized by prominent activity-dependent facilitation, which is thought to provide a wide dynamic range in hippocampal informational flow. At this synapse in mice the magnitude of paired-pulse facilitation and frequency-dependent facilitation markedly decreased with postnatal development from 3 weeks (3W) to 9 weeks (9W). Throughout this period the mean amplitude and variance of unitary EPSCs stayed constant. By altering extracellular Ca2+/Mg2+ concentrations the paired-pulse ratio could be changed to a similar extent as observed during development. However, this was accompanied by an over 30-fold change in EPSC amplitude, suggesting that the developmental change in facilitation ratio cannot simply be explained by a change in release probability. With paired-pulse stimulation the Ca2+ transients at MF terminals, monitored using mag-fura-5, showed a small facilitation, but its magnitude remained similar between 3W and 9W mice. Pharmacological tests using CNQX, adenosine, LY341495, H-7 or KN-62 suggested that neither presynaptic receptors (kainate, adenosine and metabotropic glutamate) nor protein kinases are responsible for the developmental change in facilitation. Nevertheless, loading the membrane-permeable form of BAPTA attenuated the paired-pulse facilitation in 3W mice to a much greater extent than in 9W mice, resulting in a marked reduction in age difference. These results suggest that the developmental decrease in the MF synaptic facilitation arises from a change associated with residual Ca2+, a decrease in residual Ca2+ itself or a change in Ca2+-binding sites involved in the facilitation. A developmental decline in facilitation ratio reduces the dynamic range of MF transmission, possibly contributing to the stabilization of hippocampal circuitry.
海马苔藓纤维(MF)-CA3锥体细胞突触的传递具有显著的活动依赖性易化特征,这被认为在海马信息流中提供了广泛的动态范围。在小鼠的这个突触处,从出生后3周(3W)到9周(9W),配对脉冲易化和频率依赖性易化的幅度随着出生后发育而显著降低。在此期间,单突触后电流(EPSC)的平均幅度和方差保持恒定。通过改变细胞外Ca2+/Mg2+浓度,配对脉冲比率可以改变到与发育过程中观察到的相似程度。然而,这伴随着EPSC幅度超过30倍的变化,表明易化比率的发育变化不能简单地用释放概率的变化来解释。使用配对脉冲刺激,用mag-fura-5监测MF终末的Ca2+瞬变,显示出较小的易化,但在3W和9W小鼠之间其幅度保持相似。使用CNQX、腺苷、LY341495、H-7或KN-62进行的药理学测试表明,突触前受体(海人藻酸、腺苷和代谢型谷氨酸)和蛋白激酶都与易化的发育变化无关。然而,加载膜通透性形式的BAPTA对3W小鼠配对脉冲易化的减弱程度比对9W小鼠大得多,导致年龄差异显著减小。这些结果表明,MF突触易化的发育性降低源于与残余Ca2+相关的变化、残余Ca2+本身的减少或参与易化的Ca2+结合位点的变化。易化比率的发育性下降会降低MF传递的动态范围,这可能有助于海马回路的稳定。