A robust immunofluorescence method was developed to co-immunostain multiple proteins and visualize developing myofibrils, intercalated discs, and costameres in the embryonic mouse heart.
Provides a robust immunofluorescence methodology for visualizing structural components in embryonic mouse hearts, overcoming limitations of ex vivo cultured cardiomyocyte models.
During heart development, the generation of myocardial-specific structural and functional units including sarcomeres, contractile myofibrils, intercalated discs, and costameres requires the coordinated assembly of multiple components in time and space. Disruption in assembly of these components leads to developmental heart defects. Immunofluorescent staining techniques are used commonly in cultured cardiomyocytes to probe myofibril maturation, but this ex vivo approach is limited by the extent to which myocytes will fully differentiate in culture, lack of normal in vivo mechanical inputs, and absence of endocardial cues. Application of immunofluorescence techniques to the study of developing mouse heart is desirable but more technically challenging, and methods often lack sufficient sensitivity and resolution to visualize sarcomeres in the early stages of heart development. Here, we describe a robust and reproducible method to co-immunostain multiple proteins or to co-visualize a fluorescent protein with immunofluorescent staining in the embryonic mouse heart and use this method to analyze developing myofibrils, intercalated discs, and costameres. This method can be further applied to assess cardiomyocyte structural changes caused by mutations that lead to developmental heart defects.
Wilsbacher et al. (Thu,) reported a other. Immunofluorescence technique was evaluated. A robust immunofluorescence method was developed to co-immunostain multiple proteins and visualize developing myofibrils, intercalated discs, and costameres in the embryonic mouse heart.