Life of mice – development of cardiac energetics

Production and transfer of metabolites like ATP and phosphocreatine within cardiomyocytes is crucial for the robust availability of mechanical work. In mammalian cardiomyocytes,mitochondria, themain suppliers of usable chemical energy in the form of ATP, are situated adjacent to both the ATPases near the mechanical apparatus, and the sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) calcium pumps. Operation of these ATPases requires a high ATP/ADP ratio, which is maintained by two parallel energy transfer systems – creatine kinase (CK) and direct adenine nucleotide channelling (DANC). Compartmentation of energy metabolites works to lessen the impact of dynamic changes in the availability of usable energy on the operation of these ATPases, and allows for a higher phosphorylation potential where it is required most. The operational mechanism, structure and development of the barriers responsible for energetic compartmentation within cardiomyocytes have yet to be elucidated despite intensive research in this area. A recent article in The Journal of Physiology by Piquereau et al. (2010) is an extensive investigation into how the structural and energetic properties of mouse heart muscle change during postnatal development. It includes observations on structural changes and cellular morphology using electron microscopy, quantification of mitochondrial, myofibrillar and SR proteins, assessment of organelle functionality, and the quantification of the energy flux in both the CK and DANC transfer systems. SERCA function was measured via calcium mediated tension generation, while myosin ATPase function was quantified by measuring rigor tension development. Total activity of CK and mitochondrial CK (mi-CK) were estimated. The article by Piquereau et al. builds upon a strong research tradition at Inserm U769, Univ. Paris-Sud, which focuses on studying how cardiac mechanisms function in response tobothpathological andphysiological stimuli. This includes work on contractile, sarcoplasmic reticulum (SR), and mitochondrial proteins, membrane receptors, ion channels and signalling. Their work has inspired new areas of inquiry into the function of energy compartmentation in the heart with various implications for therapeutic targets to improve both function and clinical outcomes. As main results of their recent publication, Piquereau et al. concluded that the formation of energetic microdomains occurs very early in postnatal development, and that the maturation of cellular architecture plays an important role in achieving maximal flexibility in regulation of ATP production by mitochondria. They found that the development of regulatory energetic pathways does not happen simultaneously. Throughput of energy transfer between mitochondria and myosin ATPases is correlated with the changes in the cytoarchitecture in contrast to the CK supported energy transfer which seems to depend on specific localization and expression of CK. Development between days 3 and 7 is crucial in increasing the capacity of energy transfer and involves major remodelling of the contacts between organelles. The density of intracellular organelles increases at the expense of free cytosolic space. Contacts between mitochondria and longitudinally oriented myofibrils and between SR and mitochondria are established to form an effective intracellular energetic unit. After the first week (post natum), a different phase of hypertrophy occurs without major structural changes to the contacts between organelles. After 3 weeks, the respiratory capacity ofmitochondria increases, whereas heart weight to body weight ratio decreases. The main results of the article are summarized in Fig. 1. Considerable effort has been invested by Piquereau et al. in determining various changes during cardiomyocyte maturation. Several questions arise, however, when comparing the publication with previous studies. Firstly, in 3-day-old cells, based on results from electron microscopy and SR protein expression experiments, the authors deduce SR not to be present in quantities high enough to enable SR Ca2+ content measurement. However, volumemeasurements fromelectronmicroscopy are known to be very sensitive to sample preparation procedures, especially as dimensions of different organelles can change in different ratios as a result of fixation. The low level of SR protein expression in 3-day-old cells could be explained by results obtained in embryonic mouse cardiomyocytes (Takeshima et al. 1998), where SR Ca2+ release channels do not play a major role in excitation–contraction (EC) coupling but, instead, are required for cellular Ca2+ homoestasis. Full SR function develops rapidly in neonates, possibly explaining both the dramatic increase in SR Ca2+ content between day 3 and day 7 fibres, and the difficulty the authors had in conducting the experiment with fibres from 3-day-old mice. Secondly, the authors concluded that the functional coupling of adenine nucleotide translocase (ANT) and mi-CK (‘functional activity’ in Piquereau et al. 2010) was considerably higher in adult myocytes. This conclusion, however, seems to be based on misinterpreting the KmADP/KCr ratio graph (article Fig. 5F). As is evident from the Km plots in the article (article Fig. 5E), KmCr is constant throughout the ageing process, whereas KmADP increases notably in older fibres. The increase in KmADP/KCr ratio stems from the increase of KmADP and is not, in this case, indicating increases in mi-CK–ANT coupling nor mi-CK activity. Rather, it can be interpreted as indication of an increase in diffusion restrictions to adenine nucleotides in the cytosol caused by changes in either mitochondrial outer membrane or myofibrillar and other cytosolic structures, or both (Vendelin & Birkedal, 2008; Sepp et al. 2010). In order to measure the coupling between mi-CK andANT, different experimental techniques need to be employed, such as measuring changes in respiration in response to ATP titration. Two observations can be made from further analysing SR calcium uptake and rigor tension sensitivity results from the article (article Figs 2 and 4). By looking at ratios of values obtained during different