A 3D tailored monolithic glass chip for stimulating and recording zebrafish neuronal activity with a commercial light sheet microscope

Dominika Schrödter, Mohadeseh Mozafari, Janine Fichtner, J. W. von Trotha, Reinhard Wolfgang Köster, Andreas Dietzel
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Abstract

Microfluidic technology is unrivaled in its ability to apply soluble chemical stimuli with high spatiotemporal precision. Analogous, light–sheet microscopy is unmatched in its ability of low phototoxic but fast volumetric in vivo imaging with single cell resolution. Due to their optical translucency during the larval stages, zebrafish (Danio rerio) are an ideal model to combine both techniques; yet, thus far this required light–sheet microscopes, which were in most cases custom–built and adapted to the available softlithographic chip technology. Our aim was to use a commercial light–sheet microscope to illuminate a microfluidic chip from two opposite lateral directions and to record images with the detection objective placed orthogonally above the chip. Deep tissue penetration can be achieved by superimposing beams from opposite directions to form a single light sheet. But a microfluidic chip that allows a) targeted stimulus application in a closed microenvironment, b) interference–free incoupling of excitation light from two directions and c) outcoupling of fluorescence in the perpendicular direction through an optically perfect cover glass was not known until now. Here, we present a monolithic glass chip with the required plane-parallel sidewalls and cover slide closure at the top, constructed by advanced femtosecond laser ablation, thermal bonding and surface smoothing processes. In addition, the 3D shape of a fish fixator unit was tailored to match the body shape of a zebrafish larva to ensure stable positioning during whole–brain recording. With hydrodynamic focusing a targeted partial exposure of the larva’s head to chemical stimuli and fast position switching (in less than 10 s) was possible. With the capabilities of this unique monolithic glass chip and its up–scalable wafer–level fabrication process, the new NeuroExaminer is prone to become an excellent addition to neurobiology laboratories already equipped with high–quality commercial light sheet microscopes.
用商用光片显微镜刺激和记录斑马鱼神经元活动的三维定制单片玻璃芯片
微流体技术在高时空精度的可溶性化学刺激方面具有无与伦比的能力。与此类似,光片显微镜也具有无与伦比的低光毒性和单细胞分辨率的快速体内容积成像能力。由于斑马鱼(Danio rerio)在幼鱼阶段具有光学半透明性,因此是结合这两种技术的理想模型;然而,迄今为止,这需要光片显微镜,在大多数情况下,光片显微镜都是定制的,并且要适应现有的软光刻芯片技术。我们的目标是使用商用光片显微镜从两个相反的横向方向照射微流控芯片,并通过正交放置在芯片上方的检测物镜记录图像。通过将来自相反方向的光束叠加形成单个光片,可以实现深层组织穿透。但迄今为止,还没有一种微流控芯片能实现以下功能:a) 在封闭的微环境中施加定向刺激;b) 两个方向的激发光无干扰耦合;c) 通过光学完美的盖板玻璃实现垂直方向的荧光耦合。在这里,我们展示了一种单片玻璃芯片,它具有所需的平面平行侧壁和顶部的盖玻片闭合,由先进的飞秒激光烧蚀、热粘合和表面平滑工艺制成。此外,还根据斑马鱼幼体的体形定制了鱼类固定器单元的三维形状,以确保全脑记录过程中的稳定定位。通过流体动力聚焦,可以有针对性地将幼体头部部分暴露在化学刺激下,并实现快速位置切换(不到 10 秒)。凭借这种独特的单片玻璃芯片的功能及其可升级的晶圆级制造工艺,新型 NeuroExaminer 很容易成为已配备高质量商用光片显微镜的神经生物学实验室的绝佳补充。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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