Department of Developmental Biology and Neuroscience, Tohoku University Graduate School of Life Sciences, Sendai, Japan.
PLoS One. 2013;8(3):e59179. doi: 10.1371/journal.pone.0059179. Epub 2013 Mar 21.
The calyx-type synapse of chick ciliary ganglion (CG) has been intensively studied for decades as a model system for the synaptic development, morphology and physiology. Despite recent advances in optogenetics probing and/or manipulation of the elementary steps of the transmitter release such as membrane depolarization and Ca(2+) elevation, the current gene-manipulating methods are not suitable for targeting specifically the calyx-type presynaptic terminals. Here, we evaluated a method for manipulating the molecular and functional organization of the presynaptic terminals of this model synapse. We transfected progenitors of the Edinger-Westphal (EW) nucleus neurons with an EGFP expression vector by in ovo electroporation at embryonic day 2 (E2) and examined the CG at E8-14. We found that dozens of the calyx-type presynaptic terminals and axons were selectively labeled with EGFP fluorescence. When a Brainbow construct containing the membrane-tethered fluorescent proteins m-CFP, m-YFP and m-RFP, was introduced together with a Cre expression construct, the color coding of each presynaptic axon facilitated discrimination among inter-tangled projections, particularly during the developmental re-organization period of synaptic connections. With the simultaneous expression of one of the chimeric variants of channelrhodopsins, channelrhodopsin-fast receiver (ChRFR), and R-GECO1, a red-shifted fluorescent Ca(2+)-sensor, the Ca(2+) elevation was optically measured under direct photostimulation of the presynaptic terminal. Although this optically evoked Ca(2+) elevation was mostly dependent on the action potential, a significant component remained even in the absence of extracellular Ca(2+). It is suggested that the photo-activation of ChRFR facilitated the release of Ca(2+) from intracellular Ca(2+) stores directly or indirectly. The above system, by facilitating the molecular study of the calyx-type presynaptic terminal, would provide an experimental platform for unveiling the molecular mechanisms underlying the morphology, physiology and development of synapses.
鸡睫状神经节的花萼样突触作为突触发育、形态和生理学的模型系统,已经被深入研究了几十年。尽管最近在光遗传学探测和/或操纵递质释放的基本步骤方面取得了进展,如膜去极化和 Ca(2+)升高,但目前的基因操作方法并不适合专门针对花萼样突触前末梢。在这里,我们评估了一种用于操纵这个模型突触的突触前末梢的分子和功能组织的方法。我们通过胚胎第 2 天(E2)的胚胎内电穿孔将 EGFP 表达载体转染到 Edinger-Westphal(EW)核神经元的祖细胞中,并在 E8-14 时检查 CG。我们发现,数十个花萼样突触前末梢和轴突被 EGFP 荧光选择性标记。当与 Cre 表达构建体一起引入包含膜固定荧光蛋白 m-CFP、m-YFP 和 m-RFP 的 Brainbow 构建体时,每个突触前轴突的颜色编码有助于区分交织的投射,特别是在突触连接的发育再组织期间。通过同时表达一种嵌合型通道视紫红质变体(channelrhodopsin-fast receiver,ChRFR)和 R-GECO1,一种红色偏移的荧光 Ca(2+)传感器,在直接光刺激突触前末梢时可以光学测量 Ca(2+)的升高。尽管这种光诱导的 Ca(2+)升高主要依赖于动作电位,但即使在没有细胞外 Ca(2+)的情况下,仍有显著的成分存在。这表明 ChRFR 的光激活促进了 Ca(2+)从细胞内 Ca(2+)库直接或间接地释放。该系统通过促进花萼样突触前末梢的分子研究,为揭示突触的形态、生理学和发育的分子机制提供了一个实验平台。