ABSTRACT
Investigating the function of delicate mammalian eyes often requires chemical fixation, histological sectioning, immunohistochemistry (IHC) and in situ hybridization (ISH). One of the long-standing challenges in the ocular histology field is the limited success of maintaining intact morphology via cryo- or paraffin procedures. Although our latest protocol significantly improved the morphology of mouse eyeball sections, the window technique is time-consuming and requires extensive practice to avoid damage while making windows. In this study, we present a novel glyoxal fixative that is suitable for a freeze-substitution approach to improve both morphology and molecular target preservation of mouse eyes. The method prevents morphology distortion in all tested eyeballs. Therefore, it suits a variety of research needs from morphological examination to investigation of single-molecule RNA expression, using hematoxylin and eosin (H&E) stain, IHC, and ISH assays on either frozen (cryo) or paraffin-infiltrated tissue sections. In addition, this method can be easily performed in many histology laboratories.
Acknowledgments
We thank Nancy Thomas, Karen Smith, Michael Frangello and Hannah Wilson for helping with sample and section preparation, and the Media Preparation Facility of the Stowers Institute for Medical Research for solutions preparation. We also thank Dorothy Stanley for editing the manuscript. This study is financially supported by the Stowers Institute for Medical Research.
Disclosure statement
No potential conflict of interest was reported by the author(s).
Data availability
The original data underlying this manuscript can be accessed from the Stowers Original Data Repository at http://www.stowers.org/research/publications/libpb-1715