High-resolution Immunocytochemistry of Noncollagenous Matrix Proteins in Rat Mandibles Processed with Microwave Irradiation

• Published in: The journal of histochemistry and cytochemistry Vol. 49; no. 9; pp. 1099 - 1109
• Main Authors: Arana-Chavez, Victor E, Nanci, Antonio
• Format: Journal Article
• Language: English
• Published: Los Angeles, CA Histochemical Soc 01.09.2001; SAGE Publications
• Subjects: Amelogenin; Animals; Dental Enamel Proteins - metabolism; Extracellular Matrix Proteins - metabolism; Immunohistochemistry - methods; Male; Mandible - metabolism; Mandible - ultrastructure; Microscopy, Electron; Microwaves; Rats; Rats, Wistar; Specimen Handling - methods; Tissue Embedding; Tissue Fixation; Tooth - metabolism; Tooth - ultrastructure; immunocytochemistry; noncollagenous matrix proteins; microwave processing; enamel proteins; extracellular matrix; calcified tissues
• ISSN: 0022-1554; 1551-5044
• DOI: 10.1177/002215540104900904

The mineral phase in calcified tissues represents an additional factor to be considered during their preservation for ultrastructural analyses. Microwave (MW) irradiation has been shown to facilitate fixative penetration and to improve structural preservation and immunolabeling in a variety of soft tissues. The aim of the present study was to determine whether MW processing could offer similar advantages for hard tissues. Rat hemimandibles were immersed in 4% formaldehyde + 0.1% glutaraldehyde buffered with 0.1 M sodium cacodylate, pH 7.2, and exposed to MWs for three periods of 5 min at temperatures not exceeding 37C. They were then decalcified in 4.13% EDTA, pH 7.2, for 15 hr, also under MW irradiation. Osmicated and non-osmicated samples were dehydrated in graded concentrations of ethanol and embedded in LR White resin. Sections of incisor, molars, and alveolar bone were processed for postembedding colloidal gold immunolabeling using antibodies against ameloblastin, amelogenin, bone sialoprotein, or osteopontin. Ultrastructural preservation of tissues was in most cases comparable to that obtained by perfusion-fixation, and there was no difference in distribution of labeling with those previously reported for the antibodies used. However, the immunoreactivities obtained were generally more intense, particularly at early stages of tooth formation. Amelogenin was abundant between differentiating ameloblasts and labeling for osteopontin appeared over the Golgi apparatus of odontoblasts after initiation of dentine mineralization. We conclude that MW irradiation represents a simple method that can accelerate the processing of calcified tissues while yielding good structural preservation and antigen retention. (J Histochem Cytochem 49:1099–1109, 2001)