4.7 Article

Use of High-Refractive Index Hydrogels and Tissue Clearing for Large Biological Sample Imaging

Journal

GELS
Volume 8, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/gels8010032

Keywords

hydrogel; tissue clearing; sample preparation; light sheet microscopy

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Advances in tissue clearing and light sheet fluorescence microscopy have improved our understanding of tissue morphology and disease pathology without the need for histological sectioning. This study addresses the challenges of sample handling and preservation during staining and imaging protocols by synthesizing hydrogels with a high-water content and refractive index matching typical clearing solutions. The hydrogels proved to be stable and allowed for successful imaging of cleared mouse tissues and embryos.
Recent advances in tissue clearing and light sheet fluorescence microscopy have improved insights into and understanding of tissue morphology and disease pathology by imaging large samples without the requirement of histological sectioning. However, sample handling and conservation of sample integrity during lengthy staining and acquisition protocols remains a challenge. This study overcomes these challenges with acrylamide hydrogels synthesised to match the refractive index of solutions typically utilised in aqueous tissue clearing protocols. These hydrogels have a high-water content (82.0 +/- 3.7% by weight). The gels are stable over time and FITC-IgG readily permeated into and effluxed out of them. Whilst the gels deformed and/or swelled over time in some commonly used solutions, this was overcome by using a previously described custom refractive index matched solution. To validate their use, CUBIC cleared mouse tissues and whole embryos were embedded in hydrogels, stained using fluorescent small molecule dyes, labels and antibodies and successfully imaged using light sheet fluorescence microscopy. In conclusion, the high water content, high refractive index hydrogels described in this study have broad applicability to research that delves into pathophysiological processes by stabilising and protecting large and fragile samples.

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