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Wide field-of-view volumetric imaging by a mesoscopic scanning oblique plane microscopy with switchable objective lenses

机译:通过具有可切换物镜的介观扫描倾斜平面显微镜宽视野体积成像

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Background: Conventional light sheet fluorescence microscopy (LSFM), or selective plane illumination microscopy (SPIM), enables high-resolution 3D imaging over a large volume by using two orthogonally aligned objective lenses to decouple excitation and emission. The recent development of oblique plane microscopy (OPM) simplifies LSFM design with only one single objective lens, by using off-axis excitation and remote focusing. However, most reports on OPM have a limited microscopic field of view (FOV), typically within 1×1 mm 2 . Our goal is to overcome the limitation with a new variant of OPM to achieve a mesoscopic FOV. Methods: We implemented an optical design of mesoscopic scanning OPM to allow the use of low numerical aperture (NA) objective lenses. The angle of the intermediate image before the remote focusing system was increased by a demagnification under Scheimpflug condition such that the light collecting efficiency in the remote focusing system was significantly improved. A telescope composed of cylindrical lenses was used to correct the distorted image caused by the demagnification design. We characterized the 3D resolutions and imaging volume by imaging fluorescent microspheres, and demonstrated the volumetric imaging on intact whole zebrafish larvae, mouse cortex, and multiple Caenorhabditis elegans ( C. elegans ). Results: We demonstrate a mesoscopic FOV up to ~6×5×0.6 mm 3 volumetric imaging, the largest reported FOV by OPM so far. The angle of the intermediate image plane is independent of the magnification as long as the size of the pupil aperture of the objectives is the same. As a result, the system is highly versatile, allowing simple switching between different objective lenses with low (10×, NA 0.3) and median NA (20×, NA 0.5). Detailed microvasculature in zebrafish larvae, mouse cortex, and neurons in C. elegans are clearly visualized in 3D. Conclusions: The proposed mesoscopic scanning OPM allows using low NA objectives such that centimeter-level FOV volumetric imaging can be achieved. With the extended FOV, simple sample mounting protocol, and the versatility of changeable FOVs/resolutions, our system will be ready for the varieties of applications requiring in vivo volumetric imaging over large length scales.
机译:背景技术常规光片荧光显微镜(LSFM)或选择性平面照明显微镜(SPIM)通过使用两个正交对齐的物镜来解除激发和发射,使得高分辨率在大容量上进行高分辨率的3D成像。最近倾斜平面显微镜(OPM)的开发简化了LSFM设计,只需使用一个单一物镜,通过使用离轴励磁和远程聚焦。然而,OPM上的大多数报告具有有限的微观视野(FOV),通常在1×1mm 2以内。我们的目标是克服对OPM的新变种来实现介于媒介审查的限制。方法:我们实施了介于扫描OPM的光学设计,以允许使用低数值孔径(NA)物镜。通过Scheimpflug条件下的脱磁在远程聚焦系统之前增加了中间图像的角度,使得远程聚焦系统中的光收集效率得到了显着改善。由圆柱形镜片组成的望远镜用于校正由脱磁设计引起的扭曲图像。我们通过成像荧光微球来表征了3D分辨率和成像体积,并证明了完整的整个斑马鱼幼虫,小鼠皮质和多个Caenorhabditis elegans(C. elegans)上的体积成像。结果:我们展示了一个介观FOV至0.6mm 3体积成像,最大报告的是OPM的据报道。只要物镜的瞳孔孔的尺寸是相同的,中间图像平面的角度就是偏大的。结果,该系统具有高通用,允许在不同物镜之间的简单切换,低(10×,NA 0.3)和中值Na(20×,NA 0.5)。在Zebrafish幼虫,小鼠皮质和C.Cegars中的神经元的详细微血管结构清楚地显示在3D中。结论:所提出的介观扫描OPM允许使用低NA目标,使得可以实现厘米级FOV体积成像。利用扩展FOV,简单的样品安装协议以及可变的FOVS /分辨率的多功能性,我们的系统将准备好需要在大长度尺度上体内体积成像的应用程序。

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