Exploring Immunohistochemistry in Fish: Assessment of Antibody Reactivity by Western Immunoblotting

• Published in: Animals (Basel) Vol. 13; no. 18; p. 2934
• Main Authors: Antuofermo, Elisabetta, Orioles, Massimo, Murgia, Claudio, Burrai, Giovanni P., Penati, Martina, Gottardi, Chiara, Polinas, Marta, Volpatti, Donatella, Galeotti, Marco, Addis, Maria Filippa
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.09.2023; MDPI
• Subjects: Analysis; Animals; Antibodies; antibody validation; Antigen-antibody reactions; Antigens; aquaculture; Aquaculture industry; Brain cancer; Brain research; Cloning; Cytokeratin; Fishes; GFAP; Immunohistochemistry; Keratin; Medical research; Molecular weight; Physiological aspects; Physiology; Proteins; S-100; Scientific equipment and supplies industry; Trout; Tumors; vimentin; Viral antibodies; United States; Germany; United States > US
• ISSN: 2076-2615; 2076-2615
• DOI: 10.3390/ani13182934

In recent years, research on fish has seen remarkable advancements, especially in aquaculture, ornamental fish industry, and biomedical studies. Immunohistochemistry has become crucial in fish research, aiding in physiological and pathological investigations. However, the use of antibodies originally developed for mammals has raised concerns about their cross-reactivity and specificity in fish. This study systematically evaluated the reactivity of commonly used antibodies for diagnostic purposes, especially in fish pathology, including pan-cytokeratin, vimentin, S-100, glial fibrillary acidic protein, and desmin in the tissue of Sparus aurata, Dicentrarchus labrax, Oncorhynchus mykiss, and Carassius auratus. Western immunoblotting was employed to assess antibody specificity. The results revealed that the pan-cytokeratin and glial fibrillary acidic protein antibodies cross-react with all tested fish species, while S-100 demonstrated specific staining in sea bream, goldfish, and rainbow trout tissues. Conversely, vimentin and desmin antibodies displayed no reactivity. In conclusion, the anti-cytokeratin clone AE1/AE3 and the polyclonal rabbit anti-glial fibrillary acidic protein antibody, which are extensively used in mammals, were validated for fish immunohistochemical studies. Regrettably, D33 anti-desmin and V9 anti-vimentin clones are unsuitable for immunohistochemistry in the tested fish. These findings underscore the need for species-specific antibodies and proper validation for accurate immunohistochemistry analyses in fish research.