Why the study?
In mammals, regulatory mechanisms of early heart valve and bone development contribute to adult heart valve pathologies, prompting investigation into valve interstitial cell differentiation in zebrafish.
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Population
Zebrafish from juvenile (35 days) to end of adult breeding (2.5 years) stages
Comparison
Zebrafish heart valve microarchitecture compared with adult mice
Design
Animal study using light microscopy, immunohistochemistry, and histological staining
Zebrafish valve findings warrant caution against assuming pathology; leaves open chondrogenic roles in adult mammalian valve disease.
In the heart, unidirectional blood flow depends on proper heart valve function. As, in mammals, regulatory mechanisms of early heart valve and bone development are shown to contribute to adult heart valve pathologies, we used the animal model zebrafish (ZF, Danio rerio) to investigate the microarchitecture and differentiation of cardiac valve interstitial cells in the transition from juvenile (35 days) to end of adult breeding (2.5 years) stages. Of note, light microscopy and immunohistochemistry revealed major differences in ZF heart valve microarchitecture when compared with adult mice. We demonstrate evidence for rather chondrogenic features of valvular interstitial cells by histological staining and immunodetection of SOX-9, aggrecan, and type 2a1 collagen. Collagen depositions are enriched in a thin layer at the atrial aspect of atrioventricular valves and the ventricular aspect of bulboventricular valves, respectively. At the ultrastructural level, the collagen fibrils are lacking obvious periodicity and orientation throughout the entire valve.
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Schulz et al. (2019) studied this question.
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