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使用先进成像技术对人类脑细胞解剖结构进行三维重建的不同组织透明化方法比较

Comparison of Different Tissue Clearing Methods for Three-Dimensional Reconstruction of Human Brain Cellular Anatomy Using Advanced Imaging Techniques.

作者信息

Scardigli Marina, Pesce Luca, Brady Niamh, Mazzamuto Giacomo, Gavryusev Vladislav, Silvestri Ludovico, Hof Patrick R, Destrieux Christophe, Costantini Irene, Pavone Francesco S

机构信息

European Laboratory for Non-linear Spectroscopy, University of Florence, Florence, Italy.

Department of Physics and Astronomy, University of Florence, Florence, Italy.

出版信息

Front Neuroanat. 2021 Nov 11;15:752234. doi: 10.3389/fnana.2021.752234. eCollection 2021.

Abstract

The combination of tissue clearing techniques with advanced optical microscopy facilitates the achievement of three-dimensional (3D) reconstruction of macroscopic specimens at high resolution. Whole mouse organs or even bodies have been analyzed, while the reconstruction of the human nervous system remains a challenge. Although several tissue protocols have been proposed, the high autofluorescence and variable post-mortem conditions of human specimens negatively affect the quality of the images in terms of achievable transparency and staining contrast. Moreover, homogeneous staining of high-density epitopes, such as neuronal nuclear antigen (NeuN), creates an additional challenge. Here, we evaluated different tissue transformation approaches to find the best solution to uniformly clear and label all neurons in the human cerebral cortex using anti-NeuN antibodies in combination with confocal and light-sheet fluorescence microscopy (LSFM). Finally, we performed mesoscopic high-resolution 3D reconstruction of the successfully clarified and stained samples with LSFM.

摘要

组织透明化技术与先进光学显微镜的结合有助于实现宏观标本的高分辨率三维(3D)重建。已经对整个小鼠器官甚至整个身体进行了分析,而人类神经系统的重建仍然是一项挑战。尽管已经提出了几种组织方案,但人类标本的高自发荧光和不同的死后条件在可实现的透明度和染色对比度方面对图像质量产生负面影响。此外,对高密度表位(如神经元核抗原(NeuN))进行均匀染色带来了额外的挑战。在这里,我们评估了不同的组织转化方法,以找到最佳解决方案,使用抗NeuN抗体结合共聚焦和光片荧光显微镜(LSFM)对人类大脑皮层中的所有神经元进行均匀透明化和标记。最后,我们用LSFM对成功透明化和染色的样本进行了介观高分辨率3D重建。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca4a/8632656/cae93b2e99e9/fnana-15-752234-g001.jpg

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