Rapid sonication-assisted whole tissue clearing and immunostaining.
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| Názov: | Rapid sonication-assisted whole tissue clearing and immunostaining. |
|---|---|
| Autori: | Cheung HPH; School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Sha Tin, New Territories, Hong Kong SAR, China.; Institute for Tissue Engineering and Regenerative Medicine, The Chinese University of Hong Kong, Sha Tin, New Territories, Hong Kong SAR, China.; Center for Neuromusculoskeletal Restorative Medicine, Hong Kong Science Park, Shatin, New Territories, Hong Kong SAR, China., Lauwers M; Center for Neuromusculoskeletal Restorative Medicine, Hong Kong Science Park, Shatin, New Territories, Hong Kong SAR, China., Wang Z; Research Center of Biomass 3D Printing Materials, College of Materials and Energy, South China Agricultural University, Guangzhou, 510642, China., Wang J; College of Materials Science, Hunan University, Changsha, 410082, China., Ning C; School of Materials Science and Engineering, National Engineering Research Center for Tissue Restoration and Reconstruction, South China University of Technology, Guangzhou, 510641, China., Ker DFE; Department of Biomedical Engineering, Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR, China., Wang DM; School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Sha Tin, New Territories, Hong Kong SAR, China. wangmd@cuhk.edu.hk.; Institute for Tissue Engineering and Regenerative Medicine, The Chinese University of Hong Kong, Sha Tin, New Territories, Hong Kong SAR, China. wangmd@cuhk.edu.hk.; Center for Neuromusculoskeletal Restorative Medicine, Hong Kong Science Park, Shatin, New Territories, Hong Kong SAR, China. wangmd@cuhk.edu.hk.; Department of Orthopaedics and Traumatology, Faculty of Medicine, The Chinese University of Hong Kong, Sha Tin, New Territories, Hong Kong SAR, China. wangmd@cuhk.edu.hk. |
| Zdroj: | Scientific reports [Sci Rep] 2025 Oct 08; Vol. 15 (1), pp. 35101. Date of Electronic Publication: 2025 Oct 08. |
| Spôsob vydávania: | Journal Article |
| Jazyk: | English |
| Informácie o časopise: | Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE |
| Imprint Name(s): | Original Publication: London : Nature Publishing Group, copyright 2011- |
| Výrazy zo slovníka MeSH: | Sonication*/methods , Fluorescent Antibody Technique*/methods, Animals ; Mice ; Rats ; Tendons ; Spleen |
| Abstrakt: | Competing Interests: Declarations. Competing interests: The authors declare no competing interests. High-resolution mapping of three-dimensional structures in biological tissues is essential for understanding various biological processes. However, the optical heterogeneity of these tissues, marked by varying optical properties, causes light scattering and absorption, complicating imaging. Current tissue clearing methods can take between 48 h and 32 days, and the limited diffusion depth of fluorescent probes restricts whole-tissue imaging. This study introduces an innovative Sonication-Assisted Tissue Clearing and Immunofluorescent Staining method (SoniC/S), which combines low-frequency ultrasound with a commercial chemical clearing kit and iDISCO staining techniques. When tested on the soft tissue of mouse muscle, the dense collagenous tissue of rat tendon, and the heme-rich tissue of mouse spleen, SoniC/S achieved complete clearing in just 36 h and uniform labeling in 15 h. Overall, SoniC/S provides a rapid and effective approach for tissue clearing and deep immunostaining, facilitating high-resolution volumetric imaging in biological research. (© 2025. The Author(s).) |
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| Grant Information: | ITS-020-23MX Innovation and Technology Commission of the Hong Kong SAR Government; GRF 14118620 Research Grants Council of Hong Kong SAR; N_CUHK409/23 The National Natural Science Foundation of China /Research Grants Council Joint Research Scheme |
| Contributed Indexing: | Keywords: Optical imaging; Sonication; Tissue clearing; Whole-tissue immunostaining |
| Entry Date(s): | Date Created: 20251008 Date Completed: 20251008 Latest Revision: 20251011 |
| Update Code: | 20251011 |
| PubMed Central ID: | PMC12508232 |
| DOI: | 10.1038/s41598-025-18928-5 |
| PMID: | 41062556 |
| Databáza: | MEDLINE |
| Abstrakt: | Competing Interests: Declarations. Competing interests: The authors declare no competing interests.<br />High-resolution mapping of three-dimensional structures in biological tissues is essential for understanding various biological processes. However, the optical heterogeneity of these tissues, marked by varying optical properties, causes light scattering and absorption, complicating imaging. Current tissue clearing methods can take between 48 h and 32 days, and the limited diffusion depth of fluorescent probes restricts whole-tissue imaging. This study introduces an innovative Sonication-Assisted Tissue Clearing and Immunofluorescent Staining method (SoniC/S), which combines low-frequency ultrasound with a commercial chemical clearing kit and iDISCO staining techniques. When tested on the soft tissue of mouse muscle, the dense collagenous tissue of rat tendon, and the heme-rich tissue of mouse spleen, SoniC/S achieved complete clearing in just 36 h and uniform labeling in 15 h. Overall, SoniC/S provides a rapid and effective approach for tissue clearing and deep immunostaining, facilitating high-resolution volumetric imaging in biological research.<br /> (© 2025. The Author(s).) |
|---|---|
| ISSN: | 2045-2322 |
| DOI: | 10.1038/s41598-025-18928-5 |
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