Kidokoro Yoshiaki, Kuromi Hiroshi, Delgado Ricardo, Maureira Carlos, Oliva Carolina, Labarca Pedro
Institute for Behavioral Sciences, Gunma University of School of Medicine, 3-39-22 Showa-machi, Maebashi 371-8511, Japan.
Brain Res Brain Res Rev. 2004 Dec;47(1-3):18-32. doi: 10.1016/j.brainresrev.2004.05.004.
Our knowledge on the Drosophila neuromuscular synapse is rapidly expanding. Thus, this synapse offers an excellent model for studies of the molecular mechanism of synaptic transmission and synaptic plasticity. Two synaptic vesicle (SV) pools have been identified and characterized using a fluorescent styryl dye, FM1-43, to stain SVs. They are termed the exo/endo cycling pool (ECP), which corresponds to the readily releasable pool (RRP) defined electrophysiologically, and the reserve pool (RP). These two pools were identified first in a temperature-sensitive paralytic mutant, shibire, and subsequently confirmed in wild-type larvae. The ECP participates in synaptic transmission during low frequency firing of presynaptic nerves and locates in the periphery of presynaptic boutons in the vicinity of release sites, while SVs in the RP spread toward the center of boutons and are recruited only during tetanic stimulation. These two pools are separately replenished by endocytosis. Cyclic AMP facilitates recruitment of SVs from the RP to the ECP. Activation of presynaptic metabotropic glutamate receptors recruits SVs from the RP and enhances SV release by elevation of the cAMP level. Memory mutants that have defects in the cAMP/PKA cascade, dunce and rutabaga, exhibit reduced levels of recruitment of synaptic SVs from the RP to the ECP and have limited short-term synaptic plasticity. SV mobilization between the two pools could be a key step for changes in synaptic efficacy. Since a variety of mutants that have distinct defects in synaptic transmission are available for detailed studies of synaptic function, this direction of approach in Drosophila seems promising.
我们对果蝇神经肌肉突触的了解正在迅速扩展。因此,这个突触为研究突触传递和突触可塑性的分子机制提供了一个绝佳的模型。利用一种荧光苯乙烯基染料FM1-43对突触小泡(SV)进行染色,已鉴定并表征了两个突触小泡池。它们被称为外排/内吞循环池(ECP),对应于通过电生理学定义的易释放池(RRP),以及储备池(RP)。这两个池首先在一个温度敏感的麻痹突变体“迟钝”中被鉴定出来,随后在野生型幼虫中得到证实。ECP在突触前神经低频放电期间参与突触传递,并位于释放位点附近突触前终扣的周边,而RP中的突触小泡向终扣中心扩散,仅在强直刺激期间被募集。这两个池通过内吞作用分别补充。环磷酸腺苷(cAMP)促进突触小泡从RP募集到ECP。突触前代谢型谷氨酸受体的激活从RP募集突触小泡,并通过提高cAMP水平增强突触小泡的释放。在cAMP/PKA级联反应中存在缺陷的记忆突变体“笨蛋”和“大头菜”,从RP到ECP的突触小泡募集水平降低,并且短期突触可塑性有限。两个池之间的突触小泡动员可能是突触效能变化的关键步骤。由于有多种在突触传递方面存在明显缺陷的突变体可用于详细研究突触功能,果蝇中的这种研究方向似乎很有前景。