Key result
Cultivation of rat neonatal cardiomyocytes leads to transient replacement of α-cardiac actin by α-smooth-muscle actin, which parallels the restoration of the myofibrillar system and ECM accumulation.
Does not support clinical translation of actin isoform switching; leaves open relevance to human cardiomyocyte remodeling.
Cardiomyocytes in culture undergo reversible rearrangement of their contractile apparatus with the conversion of typical myofibrils into the structures of non-muscle type and the loss of contractility. Along with these transformations, the cardiomyocytes gain the capacity to synthesize extracellular matrix. Here we show that during cultivation of rat neonatal cardiomyocytes, the inherent α-cardiac actin isoform is transiently replaced by α-smooth-muscle actin, whose expression is accompanied by transformation of myofibrils into stress-fiber-like structures. The following down-regulation of α-smooth muscle actin parallels restoration of myofibrillar system and correlates with the accumulation of extracellular collagen and laminin, initially missing from the cardiomyocytes culture.
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Bildyug et al. (2016) studied In vitro cardiomyocyte culture. In vitro cultivation was evaluated on Expression of α-smooth-muscle actin and myofibril transformation. Cultivation of rat neonatal cardiomyocytes leads to transient replacement of α-cardiac actin by α-smooth-muscle actin, which parallels the restoration of the myofibrillar system and ECM accumulation.
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