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清除后的小鼠器官的多光子显微镜成像。

Multiphoton microscopy of cleared mouse organs.

机构信息

Yale University, Department of Biomedical Engineering, New Haven, Connecticut 06520, USA.

出版信息

J Biomed Opt. 2010 May-Jun;15(3):036017. doi: 10.1117/1.3454391.

Abstract

Typical imaging depths with multiphoton microscopy (MPM) are limited to less than 300 mum in many tissues due to light scattering. Optical clearing significantly reduces light scattering by replacing water in the organ tissue with a fluid having a similar index of refraction to that of proteins. We demonstrate MPM of intact, fixed, cleared mouse organs with penetration depths and fields of view in excess of 2 mm. MPM enables the creation of large 3-D data sets with flexibility in pixel format and ready access to intrinsic fluorescence and second-harmonic generation. We present high-resolution images and 3-D image stacks of the brain, small intestine, large intestine, kidney, lung, and testicle with image sizes as large as 4,096 x 4,096 pixels.

摘要

由于光散射的原因,多光子显微镜(MPM)的典型成像深度在许多组织中限制在 300 微米以内。光学透明化通过用具有与蛋白质相似折射率的流体替代器官组织中的水,显著减少光散射。我们展示了完整、固定、透明化的小鼠器官的 MPM,其穿透深度和视场超过 2 毫米。MPM 能够创建具有像素格式灵活性的大型 3-D 数据集,并可方便地访问固有荧光和二次谐波产生。我们展示了大脑、小肠、大肠、肾脏、肺和睾丸的高分辨率图像和 3-D 图像堆栈,图像尺寸高达 4096 x 4096 像素。

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