A method for ultrafast tissue clearing that preserves fluorescence for multimodal and longitudinal brain imaging

• Published in: BMC biology Vol. 20; no. 1; p. 77
• Main Authors: Shan, Qing-Hong, Qin, Xin-Ya, Zhou, Nan, Huang, Chuan, Wang, Yu, Chen, Peng, Zhou, Jiang-Ning
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 29-03-2022; BioMed Central; BMC
• Subjects: 3D histopathology imaging; Animals; Brain; Brain - diagnostic imaging; Brain - pathology; Brain slice preparation; Circuits; Clearing; D-Sorbitol; Dyes; Fluorescence; Fluorescence enhancement; Fluorescent dyes; Fluorescent indicators; Green fluorescent protein; Health aspects; Histopathology; Image reconstruction; Image resolution; Imaging, Three-Dimensional - methods; Medical research; Methodology; Mice; Microscopy, Fluorescence - methods; Morphology; Neural circuitry; Neuro-circuit tracing; Neuroimaging; Neuroimaging - methods; Optical Imaging - methods; Organs; Physiological aspects; Proteins; Reagents; Sorbitol; Three dimensional imaging; Three-dimensional visualisation; Tissues; Tomography; Ultrafast tissue clearing; China; Three-dimensional visualisation; Neuro-circuit tracing; Ultrafast tissue clearing; 3D histopathology imaging; Fluorescence enhancement
• ISSN: 1741-7007; 1741-7007
• DOI: 10.1186/s12915-022-01275-6

Tissue-clearing techniques have recently been developed to make tissues transparent for three-dimensional (3D) imaging at different scales, including single-cell resolution. However, current tissue-clearing workflows have several disadvantages, including complex protocols, time-consuming application, and fluorescence quenching. Additionally, they can be used mainly for clearing larger-volume samples, preventing wide and easy applicability in conventional experimental approaches. In this study, we aimed to develop a versatile, fast, and convenient method for clearing thin and semi-thick samples, which can be used for three-dimensional imaging of experimental or even clinical samples.
We developed an alkaline solution (AKS) containing a combination of 2,2'-thiodiethanol (TDE), DMSO, D-sorbitol, and Tris for tissue clearing, as the alkaline environment is suitable for maintaining the fluorescence of most commonly used fluorescence protein GFP and its variants, and tested its clearing effect on samples from mice and human brains. We assessed the clearing speed, the preservation of fluorescence protein and dyes, and the imaging depth and quality. The results showed that AKS treatment rapidly cleared 300-μm-thick brain slices and 1-mm-thick slices from different organs within 5 min and 1 h, respectively. Moreover, AKS was compatible with a variety of fluorescence proteins and dyes. Most importantly, AKS enhanced the fluorescence of YFP, in contrast to the majority of existing tissue-clearing methods which reduce the fluorescence intensity of fluorescent proteins. Using AKS, we performed long-time high-resolution imaging of weak fluorescent protein-labelled tissues, long-distance fibre tracking, larger-scale 3D imaging and cell counting of the entire brain area, neural circuit tracing, 3D neuromorphic reconstruction, and 3D histopathology imaging.
AKS can be used for simple and rapid clearing of samples from mice and human brains and is widely compatible with a variety of fluorescent dyes. Therefore, AKS has great potential to be used as a broad tissue-clearing reagent for biological optical imaging, especially for time-sensitive experiments.