Glial fibrillary acidic protein expression in pleomorphic adenoma of salivary gland: an immunoelectron microscopic study

• Published in: Ultrastructural pathology Vol. 14; no. 3; p. 263
• Main Authors: Anderson, C, Knibbs, D R, Abbott, S J, Pedersen, C, Krutchkoff, D
• Format: Journal Article
• Language: English
• Published: England 01.01.1990
• Subjects: Adenoma - analysis; Adenoma - ultrastructure; Epithelium - ultrastructure; Glial Fibrillary Acidic Protein - analysis; Humans; Immunoenzyme Techniques; Immunohistochemistry; Microscopy, Electron; Salivary Gland Neoplasms - analysis; Salivary Gland Neoplasms - ultrastructure; Vimentin - analysis
• ISSN: 0191-3123
• DOI: 10.3109/01913129009076130

Previous immunocytochemical studies of pleomorphic adenomas have demonstrated consistent labeling with glial fibrillary acidic protein (GFAP). Cross-reactivity with other intermediate filaments of similar structure and chemical composition has been suggested to account for this seemingly inappropriate pattern of immunoreactivity. To investigate further this phenomenon, we examined five pleomorphic adenomas by immunoelectron microscopy. Ultrastructural features were similar to those described by other investigators, with ductal epithelium being surrounded by myoepithelial cells and modified cells becoming detached to form the isolated stellate and spindle cells of the stroma. As part of this process, many neoplastic myoepithelial cells appeared to lose their specialized ultrastructural features, assuming a rather undifferentiated appearance. Single and double immunoelectron microscopic labeling showed vimentin filaments in all these neoplastic myoepithelial cells. In contrast, GFAP filaments were identified only in the most undifferentiated cells. Such restriction of GFAP filaments to an ultrastructurally definable subset of neoplastic cells provides strong evidence against nonspecific staining due to cross-reactivity. Given the previously described coexpression of vimentin and GFAP by neoplastic cartilage, it appears likely that this immunophenotype in neoplastic myoepithelial cells reflects early chondroid differentiation.