4.3 Article

Chemical fluorescence-based dye staining for 3-dimensional histopathology analysis

Journal

ANIMAL CELLS AND SYSTEMS
Volume 26, Issue 2, Pages 45-51

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/19768354.2022.2049641

Keywords

Chemical dye; eosin; tissue clearing; histopathology

Funding

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [NRF2021R1A2C1010677, NRF-2021M3E5D9021368]

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Tissue clearing for 3D imaging is widely used in biomedical applications, but immunofluorescence labeling of thick specimens is time-consuming. Using low molecular weight chemical dyes can expedite the 3D labeling process. The combination of SYTO 16 and eosin (S&E) was found to be a potential fluorescent alternative to the traditional hematoxylin-eosin (H&E) stain. Additionally, other chemical dyes like picrosirius red, Congo red, and fluorescent Nissl can be used alone or in combination with antibody labeling for tissue clearing.
Tissue clearing for 3-dimensional (3D) imaging is increasingly utilized in many biomedical applications, including the pathological examination of human biopsy specimens. Although many protocols offer rapid and efficient tissue clearing (>1 d), immunofluorescence labeling of thick specimens is a highly time-consuming process. The use of low molecular weight chemical dyes has potential benefits in terms of speed and quality of 3D labeling. Accordingly, we tested several chemical dyes to assess their potential applications in 3D imaging. The combination of SYTO 16 and eosin (S&E) was found to be a potential fluorescent version of the hematoxylin-eosin (H&E) stain. Furthermore, picrosirius red (for collagen), Congo red (for senile plaques), and fluorescent Nissl (for neurons in the normal brain or blood vessels in the injured brain) stains can be used alone or in combination with antibody labeling. As chemical labeling requires a relatively short incubation time (<1 d), fluorescent chemical dyes could expedite the 3D imaging process.

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