Lin Tzu-Yang, Luo Jiangnan, Shinomiya Kazunori, Ting Chun-Yuan, Lu Zhiyuan, Meinertzhagen Ian A, Lee Chi-Hon
Section on Neuronal Connectivity, Laboratory of Gene Regulation and Development, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, 20892.
Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, 114, Taiwan.
J Comp Neurol. 2016 Feb 1;524(2):213-27. doi: 10.1002/cne.23857. Epub 2015 Aug 11.
In Drosophila, color vision and wavelength-selective behaviors are mediated by the compound eye's narrow-spectrum photoreceptors R7 and R8 and their downstream medulla projection (Tm) neurons Tm5a, Tm5b, Tm5c, and Tm20 in the second optic neuropil or medulla. These chromatic Tm neurons project axons to a deeper optic neuropil, the lobula, which in insects has been implicated in processing and relaying color information to the central brain. The synaptic targets of the chromatic Tm neurons in the lobula are not known, however. Using a modified GFP reconstitution across synaptic partners (GRASP) method to probe connections between the chromatic Tm neurons and 28 known and novel types of lobula neurons, we identify anatomically the visual projection neurons LT11 and LC14 and the lobula intrinsic neurons Li3 and Li4 as synaptic targets of the chromatic Tm neurons. Single-cell GRASP analyses reveal that Li4 receives synaptic contacts from over 90% of all four types of chromatic Tm neurons, whereas LT11 is postsynaptic to the chromatic Tm neurons, with only modest selectivity and at a lower frequency and density. To visualize synaptic contacts at the ultrastructural level, we develop and apply a "two-tag" double-labeling method to label LT11's dendrites and the mitochondria in Tm5c's presynaptic terminals. Serial electron microscopic reconstruction confirms that LT11 receives direct contacts from Tm5c. This method would be generally applicable to map the connections of large complex neurons in Drosophila and other animals.
在果蝇中,颜色视觉和波长选择性行为由复眼中窄光谱的光感受器R7和R8及其在第二视神经节或髓质中的下游髓质投射(Tm)神经元Tm5a、Tm5b、Tm5c和Tm20介导。这些色觉Tm神经元将轴突投射到更深的视神经节小叶,在昆虫中,小叶与处理和向中枢脑传递颜色信息有关。然而,小叶中色觉Tm神经元的突触靶点尚不清楚。我们使用一种改进的跨突触伙伴绿色荧光蛋白重组(GRASP)方法来探测色觉Tm神经元与28种已知和新型小叶神经元之间的连接,从解剖学上确定了视觉投射神经元LT11和LC14以及小叶固有神经元Li3和Li4是色觉Tm神经元的突触靶点。单细胞GRASP分析显示,Li4接收来自所有四种色觉Tm神经元中超过90%的突触接触,而LT11是色觉Tm神经元的突触后神经元,选择性适中,频率和密度较低。为了在超微结构水平上观察突触接触,我们开发并应用了一种“双标记”双标记方法来标记LT11的树突和Tm5c突触前终末中的线粒体。连续电子显微镜重建证实LT11直接接受Tm5c的接触。这种方法通常适用于绘制果蝇和其他动物中大型复杂神经元的连接图谱。