Kuromi Hiroshi, Kidokoro Yoshi
Gunma University School of Medicine, 3-39-22 Showa-machi, Maebashi 371-8511, Japan.
J Neurocytol. 2003 Jun-Sep;32(5-8):551-65. doi: 10.1023/B:NEUR.0000020610.13554.3c.
Drosophila neuromuscular junctions ( D NMJs) are malleable and its synaptic strength changes with activities. Mobilization and recruitment of synaptic vesicles (SVs), and replenishment of SV pools in the presynaptic terminal are involved in control of synaptic efficacy. We have studied dynamics of SVs using a fluorescent styryl dye, FM1-43, which is loaded into SVs during endocytosis and released during exocytosis, and identified two SV pools. The exo/endo cycling pool (ECP) is loaded with FM1-43 during low frequency nerve stimulation and releases FM1-43 during exocytosis induced by high K(+). The ECP locates close to release sites in the periphery of presynaptic boutons. The reserve pool (RP) is loaded and unloaded only during high frequency stimulation and resides primarily in the center of boutons. The size of ECP closely correlates with the efficacy of synaptic transmission during low frequency neuronal firing. An increase of cAMP facilitates SV movement from RP to ECP. Post-tetanic potentiation (PTP) correlates well with recruitment of SVs from RP. Neither PTP nor post-tetanic recruitment of SVs from RP occurs in memory mutants that have defects in the cAMP/PKA cascade. Cyotochalasin D slows mobilization of SVs from RP, suggesting involvement of actin filaments in SV movement. During repetitive nerve stimulation the ECP is replenished, while RP replenishment occurs after tetanic stimulation in the absence of external Ca(2+). Mobilization of internal Ca(2+) stores underlies RP replenishment. SV dynamics is involved in synaptic plasticity and D NMJs are suitable for further studies.
果蝇神经肌肉接头(D NMJs)具有可塑性,其突触强度会随活动而变化。突触小泡(SVs)的动员和募集以及突触前终末中SV池的补充参与了突触效能的控制。我们使用一种荧光苯乙烯基染料FM1-43研究了SVs的动力学,该染料在胞吞过程中被装载到SVs中,并在胞吐过程中释放,同时鉴定出了两个SV池。外排/内吞循环池(ECP)在低频神经刺激期间装载FM1-43,并在高钾(K⁺)诱导的胞吐过程中释放FM1-43。ECP位于突触前终扣外周靠近释放位点的位置。储备池(RP)仅在高频刺激期间装载和卸载,主要位于终扣的中心。ECP的大小与低频神经元放电期间突触传递的效能密切相关。环磷酸腺苷(cAMP)的增加促进了SVs从RP向ECP的移动。强直后增强(PTP)与从RP募集SVs密切相关。在cAMP/蛋白激酶A(PKA)级联反应存在缺陷的记忆突变体中,既不发生PTP,也不发生从RP的强直后SVs募集。细胞松弛素D减缓了SVs从RP的动员,表明肌动蛋白丝参与了SVs的移动。在重复神经刺激期间,ECP会得到补充,而在没有外部钙离子(Ca²⁺)的情况下,强直刺激后RP会得到补充。内部钙离子储存的动员是RP补充的基础。SVs动力学参与了突触可塑性,D NMJs适合进一步研究。