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Publication : Novel large-particle FACS purification of adult ventricular myocytes reveals accumulation of myosin and actin disproportionate to cell size and proteome in normal post-weaning development.

First Author  López JE Year  2017
Journal  J Mol Cell Cardiol Volume  111
Pages  114-122 PubMed ID  28780067
Mgi Jnum  J:253733 Mgi Id  MGI:6102478
Doi  10.1016/j.yjmcc.2017.07.012 Citation  Lopez JE, et al. (2017) Novel large-particle FACS purification of adult ventricular myocytes reveals accumulation of myosin and actin disproportionate to cell size and proteome in normal post-weaning development. J Mol Cell Cardiol 111:114-122
abstractText  RATIONALE: Quantifying cellular proteins in ventricular myocytes (MCs) is challenging due to tissue heterogeneity and the variety of cell sizes in the heart. In post-weaning cardiac ontogeny, rod-shaped MCs make up the majority of the cardiac mass while remaining a minority of cardiac cells in number. Current biochemical analyses of cardiac proteins do not correlate well the content of MC-specific proteins to cell type or size in normally developing tissue. OBJECTIVE: To develop a new large-particle fluorescent-activated cell sorting (LP-FACS) strategy for the purification of adult rod-shaped MCs. This approach is developed to enable growth-scaled measurements per-cell of the MC proteome and sarcomeric proteins (i.e. myosin heavy chain (MyHC) and alpha-actin (alpha-actin)) content. METHODS AND RESULTS: Individual cardiac cells were isolated from 21 to 94days old mice. An LP-FACS jet-in-air system with a 200-mum nozzle was defined for the first time to purify adult MCs. Cell-type specific immunophenotyping and sorting yielded >/=95% purity of adult MCs independently of cell morphology and size. This approach excluded other cell types and tissue contaminants from further analysis. MC proteome, MyHC and alpha-actin proteins were measured in linear biochemical assays normalized to cell numbers. Using the allometric coefficient alpha, we scaled the MC-specific rate of protein accumulation to growth post-weaning. MC-specific volumes (alpha=1.02) and global protein accumulation (alpha=0.94) were proportional (i.e. isometric) to body mass. In contrast, MyHC and alpha-actin accumulated at a much greater rate (i.e. hyperallometric) than body mass (alpha=1.79 and 2.19 respectively) and MC volumes (alpha=1.76 and 1.45 respectively). CONCLUSION: Changes in MC proteome and cell volumes measured in LP-FACS purified MCs are proportional to body mass post-weaning. Oppositely, MyHC and alpha-actin are concentrated more rapidly than what would be expected from MC proteome accumulation, cell enlargement, or animal growth alone. LP-FACS provides a new standard for adult MC purification and an approach to scale the biochemical content of specific proteins or group of proteins per cell in enlarging MCs.
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