Key result
Binucleate cardiomyocytes show asymmetric protein clustering and single-nucleus calcium initiation, suggesting distinct nuclear roles.
Why the study?
The role of binucleate cardiomyocytes in myocardial repair and their protein synthesis activity during development and stress is not well understood.
Protein clustering to a single nucleus in binucleate cardiomyocytes suggests differential nuclear roles, which may have implications for myocardial repair and stem cell therapy.
Should not yet change clinical practice for myocardial repair; leaves open whether nuclear specialization aids human cardiomyocyte regeneration.
Neonatal and adult cardiomyocytes were isolated from rat hearts. Some of the adult myocytes were cultured to allow for cell dedifferentiation, a phenomenon thought to mimic cell changes that occur in stressed myocardium, with myocytes regressing to a fetal pattern of metabolism and stellate neonatal shape.Using fluorescence deconvolution microscopy, cells were probed with fluorescent markers and scanned for a number of proteins associated with ion control, calcium movements and cardiac function. Image analysis of deconvoluted image stacks and sequential real-time image recordings of calcium transients of cells were made.All three myocyte groups were predominantly comprised of binucleate cells. Clustering of proteins to a single nucleus was a common observation, suggesting that one nucleus is active in protein synthesis pathways, while the other nucleus assumes a 'dormant' or different role and that cardiomyocytes might be mitotically active even in late development, or specific protein syntheses could be targeted and regulated for reintroduction into the cell cycle.Such possibilities would extend cardiac disease associated stem cell research and therapy options, while producing valuable insights into developmental and death pathways of binucleate cardiomyocytes (word count 183).
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Stephen et al. (2009) studied Myocardial repair and cardiomyocyte biology. Cell culture and dedifferentiation vs. Freshly isolated adult and neonatal cardiomyocytes was evaluated on Protein localization and calcium transient initiation in binucleate cardiomyocytes. Binucleate cardiomyocytes demonstrate clustering of specific proteins and calcium transient initiation around a single nucleus, suggesting distinct functional roles for each nucleus in cellular maturation and potential myocardial repair.
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