Immunocytochemistry to study myogenesis in zebrafish

• Published in: Methods in molecular biology (Clifton, N.J.) Vol. 798; p. 153
• Main Authors: Bird, Nathan C, Windner, Stefanie E, Devoto, Stephen H
• Format: Journal Article
• Language: English
• Published: United States 2012
• Subjects: Animals; Embryo, Nonmammalian - cytology; Embryo, Nonmammalian - metabolism; Immunohistochemistry - methods; Muscle Development - physiology; Tissue Fixation - methods; Zebrafish - embryology; Zebrafish Proteins - analysis
• ISSN: 1940-6029
• DOI: 10.1007/978-1-61779-343-1_9

During myogenesis, cells gradually transition from mesodermal precursors to myoblasts, myocytes, and then to muscle fibers. The molecular characterization of this process requires the ability to identify each of these cell types and the factors that regulate the transitions between them. The most versatile technique for assaying cell identities in situ is immunocytochemistry, because multiple independent molecular markers of differentiation can be assayed simultaneously. The zebrafish has developed into a popular model for the study of myogenesis, and immunocytochemical techniques have been critical. We have adapted existing protocols to optimize immunocytochemistry in zebrafish, and have tested many antibodies developed against mouse, chick, and frog muscle antigens for their cross-reactivity in zebrafish. Here, we present protocols for whole mount immunocytochemistry on both formaldehyde and Carnoy's fixed embryos as well as on sectioned zebrafish tissue. We include a table of antibodies useful for experiments on the molecular biology of myogenesis in zebrafish.