Bonanomi Dario, Pennuto Maria, Rigoni Michela, Rossetto Ornella, Montecucco Cesare, Valtorta Flavia
Department of Neuroscience, San Raffaele Scientific Institute, via Olgettina 58, 20132 Milan, Italy.
Mol Pharmacol. 2005 Jun;67(6):1901-8. doi: 10.1124/mol.104.005678. Epub 2005 Feb 4.
The application of the snake neurotoxin taipoxin to hippocampal neurons in culture induced Ca(2+)-dependent synaptic vesicle (SV) exocytosis, with swelling of nerve terminals and redistribution of SV proteins to the axolemma. Using digital imaging videomicroscopy to measure fluorescence resonance energy transfer in live neurons, we also found that taipoxin modulates the machinery for neurosecretion by causing dissociation of the SV proteins synaptobrevin 2 and synaptophysin I at a stage preceding taipoxin-induced facilitation of SV fusion. These early effects of the toxin are followed by severe impairment of SV exo-endocytosis, which might underlie the prevention of neurotransmitter release reported after intoxication by taipoxin.
将蛇神经毒素太攀蛇毒素应用于培养的海马神经元,可诱导依赖钙离子的突触小泡(SV)胞吐作用,同时伴有神经末梢肿胀以及SV蛋白重新分布至轴膜。利用数字成像视频显微镜测量活神经元中的荧光共振能量转移,我们还发现太攀蛇毒素通过在其诱导SV融合促进之前的阶段导致SV蛋白突触结合蛋白2和突触素I解离,从而调节神经分泌机制。毒素的这些早期作用之后是SV胞吐-内吞作用的严重受损,这可能是太攀蛇毒素中毒后报道的神经递质释放受到抑制的基础。