Department of Chemistry, McGill University, 801 Sherbrooke Street West, H3A 2K6 Montreal, Canada.
ACS Chem Neurosci. 2010 Feb 17;1(2):86-94. doi: 10.1021/cn900011n. Epub 2009 Oct 15.
The formation of functional synapses on artificial substrates is a very important step in the development of engineered in vitro neural networks. Spherical supported bilayer lipid membranes (SS-BLMs) are used here as a novel substrate to demonstrate presynaptic vesicle accumulation at an in vitro synaptic junction. Confocal fluorescence microscopy, cryo-transmission electron microscopy (cryo-TEM), and fluorescence recovery after photobleaching (FRAP) experiments have been used to characterize the SS-BLMs. Conventional immunocytochemistry combined with confocal fluorescence microscopy was used to observe the formation of presynaptic vesicles at the neuron-SS-BLM contacts. These results indicate that lipid phases may play a role in the observed phenomenon, in addition to the chemical and electrostatic interactions between the neurons and SS-BLMs. The biocompatibility of lipid bilayers along with their membrane tunability makes the suggested approach a useful "toolkit" for many neuroengineering applications including artificial synapse formation and synaptogenesis in vivo.
在人工基质上形成功能性突触是体外神经回路工程发展的一个非常重要的步骤。本文使用球形支撑双层脂质膜(SS-BLM)作为一种新型基质,来证明体外突触连接处的突触小泡的积累。共聚焦荧光显微镜、冷冻透射电子显微镜(cryo-TEM)和光漂白荧光恢复(FRAP)实验被用来对 SS-BLM 进行表征。常规免疫细胞化学结合共聚焦荧光显微镜被用于观察神经元与 SS-BLM 接触处突触小泡的形成。这些结果表明,除了神经元和 SS-BLM 之间的化学和静电相互作用之外,脂质相可能在观察到的现象中起作用。脂质双层的生物相容性及其膜可调性使得所提出的方法成为许多神经工程应用的有用“工具包”,包括人工突触形成和体内突触发生。