Tong James Jiayuan
Biophysics and Physiology, University of California, Irvine, CA 92697, USA.
Biol Bull. 2007 Apr;212(2):169-75. doi: 10.2307/25066594.
Mitochondria, as portable generators that power synaptic function, regulate the ATP supply and calcium homeostasis in the neuron. As molecular interactions within the synapses before and after the potentiation are beginning to be elucidated, the deciding moment during the tetanic stimulation that gives rise to the strengthening of the synapse remains a mystery. Here, I recorded electrically from an intact Drosophila nervous system, while simultaneously using time-lapse confocal microscopy to visualize mitochondria labeled with green fluorescent protein. I show that tetanic stimulation triggers a fast delivery of mitochondria to the synapse, which facilitates synaptic potentiation. Rotenone, an inhibitor of mitochondrial electron transport chain complex I, suppresses mitochondrial transport and abolishes the potentiation of the synapse. Expression of neurofibromin, which improves mitochondrial ATP synthesis in the neuron, enhances the movements of mitochondria to the synapse and promotes post-tetanic potentiation. These findings provide unprecedented evidence that the mitochondrial delivery to the synapse is critical for cellular learning.
线粒体作为为突触功能提供能量的便携式发电机,调节神经元中的ATP供应和钙稳态。随着突触增强前后突触内分子相互作用开始得到阐明,强直刺激期间导致突触增强的决定性时刻仍是一个谜。在这里,我在完整的果蝇神经系统中进行电记录,同时使用延时共聚焦显微镜观察用绿色荧光蛋白标记的线粒体。我发现强直刺激会触发线粒体快速运输到突触,这有助于突触增强。鱼藤酮是线粒体电子传递链复合体I的抑制剂,它会抑制线粒体运输并消除突触增强。神经纤维瘤蛋白的表达可改善神经元中的线粒体ATP合成,增强线粒体向突触的移动并促进强直后增强。这些发现提供了前所未有的证据,表明线粒体运输到突触对细胞学习至关重要。