Laboratory of Molecular Synaptic Function, Doshisha University Graduate School of Brain Science, Kyotanabe 610-0394, Japan.
Neuron. 2012 Nov 8;76(3):511-7. doi: 10.1016/j.neuron.2012.08.013.
After releasing neurotransmitter, synaptic vesicles are retrieved by endocytosis and recycled via fast and slow pathways to be reused for synaptic transmission. To maintain the synaptic efficacy, vesicles must be refilled with neurotransmitter during recycling. However, the refilling speed estimated in isolated or reconstructed vesicles is, thus far, too slow to fill up vesicles within the period of recycling. Here, we re-examined the vesicle refilling rate directly at central glutamatergic synapses in slices, using simultaneous presynaptic and postsynaptic whole-cell recording combined with caged glutamate photolysis. After washing out vesicular glutamate, refilling of vesicles with uncaged glutamate caused a recovery of EPSCs with a time constant of 15 s that varied depending upon temperature, age, and cytosolic Cl(-) concentrations. This time constant is faster than that of the slow recycling pathway (∼30 s) after clathrin-mediated endocytosis but is much too slow to fill up vesicles replenished through fast recycling pathways (<1 s).
神经递质释放后,突触囊泡通过胞吞作用被回收,并通过快速和慢速途径循环利用,以重新用于突触传递。为了维持突触效能,囊泡在循环过程中必须重新充满神经递质。然而,迄今为止,在分离或重建的囊泡中估计的填充速度太慢,无法在循环期间填满囊泡。在这里,我们使用同时进行的突触前和突触后全细胞记录以及笼状谷氨酸光解,在切片中直接重新检查了中央谷氨酸能突触中的囊泡填充速率。在用囊泡谷氨酸洗脱后,未笼状的谷氨酸填充囊泡会引起 EPSC 的恢复,其时间常数为 15 秒,该时间常数取决于温度、年龄和细胞溶质 Cl(-)浓度。该时间常数快于网格蛋白介导的胞吞作用后的慢速循环途径(约 30 秒),但远慢于通过快速循环途径补充的囊泡填充速度(<1 秒)。
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