Girstmair Johannes, Zakrzewski Anne, Lapraz François, Handberg-Thorsager Mette, Tomancak Pavel, Pitrone Peter Gabriel, Simpson Fraser, Telford Maximilian J
Department of Genetics, Evolution and Environment, University College London, London, WC1E 6BT, UK.
CNRS, CBD UMR5547, Université de Toulouse, UPS, Centre de Biologie du Développement, Bâtiment 4R3, 118 Route de Narbonne, 31062, Toulouse, France.
BMC Dev Biol. 2016 Jun 30;16(1):22. doi: 10.1186/s12861-016-0122-0.
Selective plane illumination microscopy (SPIM a type of light-sheet microscopy) involves focusing a thin sheet of laser light through a specimen at right angles to the objective lens. As only the thin section of the specimen at the focal plane of the lens is illuminated, out of focus light is naturally absent and toxicity due to light (phototoxicity) is greatly reduced enabling longer term live imaging. OpenSPIM is an open access platform (Pitrone et al. 2013 and OpenSPIM.org) created to give new users step-by-step instructions on building a basic configuration of a SPIM microscope, which can in principle be adapted and upgraded to each laboratory's own requirements and budget. Here we describe our own experience with the process of designing, building, configuring and using an OpenSPIM for our research into the early development of the polyclad flatworm Maritigrella crozieri - a non-model animal.
Our OpenSPIM builds on the standard design with the addition of two colour laser illumination for simultaneous detection of two probes/molecules and dual sided illumination, which provides more even signal intensity across a specimen. Our OpenSPIM provides high resolution 3d images and time lapse recordings, and we demonstrate the use of two colour lasers and the benefits of two color dual-sided imaging. We used our microscope to study the development of the embryo of the polyclad flatworm M. crozieri. The capabilities of our microscope are demonstrated by our ability to record the stereotypical spiral cleavage pattern of M. crozieri with high-speed multi-view time lapse imaging. 3D and 4D (3D + time) reconstruction of early development from these data is possible using image registration and deconvolution tools provided as part of the open source Fiji platform. We discuss our findings on the pros and cons of a self built microscope.
We conclude that home-built microscopes, such as an OpenSPIM, together with the available open source software, such as MicroManager and Fiji, make SPIM accessible to anyone interested in having continuous access to their own light-sheet microscope. However, building an OpenSPIM is not without challenges and an open access microscope is a worthwhile, if significant, investment of time and money. Multi-view 4D microscopy is more challenging than we had expected. We hope that our experience gained during this project will help future OpenSPIM users with similar ambitions.
选择性平面照明显微镜(SPIM,一种光片显微镜)涉及将一束薄的激光以与物镜成直角的方式聚焦穿过标本。由于仅标本位于透镜焦平面的薄切片被照亮,离焦光自然不存在,并且光毒性(因光导致的毒性)大大降低,从而能够进行更长期的活细胞成像。OpenSPIM是一个开放获取平台(皮特罗内等人,2013年;OpenSPIM.org),旨在为新用户提供关于构建SPIM显微镜基本配置的逐步指导,原则上可根据每个实验室的自身要求和预算进行调整和升级。在此,我们描述我们自己在设计、构建、配置和使用一台OpenSPIM用于研究多肠目扁形虫克罗齐氏海扁虫(一种非模式动物)早期发育过程中的经验。
我们的OpenSPIM在标准设计的基础上增加了双色激光照明,用于同时检测两种探针/分子以及双面照明,这使得标本上的信号强度更加均匀。我们的OpenSPIM提供高分辨率的三维图像和延时记录,并且我们展示了双色激光的使用以及双色双面成像的优势。我们使用我们的显微镜研究了多肠目扁形虫克罗齐氏海扁虫胚胎的发育。我们通过能够以高速多视角延时成像记录克罗齐氏海扁虫典型的螺旋卵裂模式,展示了我们显微镜的性能。利用作为开源Fiji平台一部分提供的图像配准和去卷积工具,可以从这些数据对早期发育进行三维和四维(三维 + 时间)重建。我们讨论了关于自制显微镜优缺点的研究结果。
我们得出结论,自制显微镜,如OpenSPIM,连同可用的开源软件,如MicroManager和Fiji,使任何有兴趣持续使用自己的光片显微镜的人都能够使用SPIM。然而,构建一台OpenSPIM并非没有挑战,而且一台开放获取的显微镜是一项值得投入时间和资金的重大投资。多视角四维显微镜比我们预期的更具挑战性。我们希望我们在这个项目中获得的经验将帮助未来有类似抱负的OpenSPIM用户。