No abstract

No abstract

No abstract

The cheek pouch is an anatomical peculiarity of hamsters, widely used as an experimental model for oral cancer, and characterization of its normal cell populations and the changes they undergo in pathological conditions is of great interest. Our studies of epithelium-connective tissue interactions have revealed that hamster eosinophils are not easily recognizable because they are small and exhibit a larger nucleus:cytoplasm ratio than those in human and other animal tissues. Luna's technique is the most popular specific staining technique for eosinophils. Owing to the morphology of hamster eosinophils, however, it was necessary to modify Luna's technique to stain these cells selectively against a more contrasting background that would enable their identification and quantitation in the hamster cheek pouch. The modification involved staining the sections with a solution of 0.5% Biebrich scarlet in lithium carbonate followed by counterstaining with 1% metanil yellow in water. The eosinophils were stained selectively red against a yellow background. Our technique avoided nuclear staining and enhanced observation of selectively stained granules in a scarce cytoplasm with a contrasting background, which permits fast, reproducible studies and automated image analysis.

Silver staining of nucleolar organizer regions (NORs) and their subsequent quantification by image analysis are used increasingly in human pathological specimens and experimental models. Because certain conditions determined by the type of tissue and/or its fixation render AgNOR segmentation for image analysis difficult due to insufficient contrast or nonspecific silver precipitation, we propose three improvements to the original technique to overcome these difficulties. Pretreatment with 7% nitric acid produced very distinct dark brown images of AgNORs on a yellow background. The gradient of background colors allowed easy discrimination of nucleolar, nuclear and cytoplasmic structures. Seven morphometric parameters related to number, size and shape of AgNORs were evaluated quantitatively by image analysis on sections pretreated with nitric acid and on adjacent sections treated with citrate buffer in a wet autoclave according to the most widely accepted method for image analysis of AgNOR. Both methods yielded similar results. A second improvement was achieved by coating the slides with 7% celloidin solution in ethyl alcohol-ether prior to AgNOR staining and acid pretreatment. This coating prevented nonspecific silver deposition on argyrophilic bacteria and other tissue debris in human vaginal smears that could make visualizing AgNOR sites difficult. Finally, placing sections face down on the staining solution prevents the formation of nonspecific silver precipitates. These procedures can be applied together or separately according to the requirements of the material to be evaluated.