Abstract

RationaleThe extent of heart disease varies from person to person, suggesting that genetic background is important in pathology. Genetic background is also important when selecting appropriate mouse models to study heart disease. This study examines heart growth as a function of strain, specifically C57BL/6 and DBA/2 mouse strains.ObjectiveIn this study, we test the hypothesis that two strains of mice, C57BL/6 and DBA/2, will produce varying degrees of heart growth in both physiological and pathological settings.Methods and ResultsDifferences in heart dimensions are detectable by echocardiography at 8 weeks of age. Percentages of cardiac progenitor cells (c-kit+ cells) and mononucleated cells were found to be in a higher percentage in DBA/2 mice, and more tri- and quad-nucleated cells were in C57BL/6 mice. Cardiomyocyte turnover shows no significant changes in mitotic activity, however, there is more apoptotic activity in DBA/2 mice. Cardiomyocyte cell size increased with age, but increased more in DBA/2 mice, although percentages of nucleated cells remained the same in both strains. Two-week isoproterenol stimulation showed an increase in heart growth in DBA/2 mice, both at cardiomyocyte and whole heart level. In isoproterenol-treated DBA/2 mice, there was also a greater expression level of the hypertrophy marker, ANF, compared to C57BL/6 mice.ConclusionWe conclude that the DBA/2 mouse strain has a more immature cardiac phenotype, which correlates to a cardiac protective response to hypertrophy in both physiological and pathological stimulations.

Highlights

  • The heart undergoes structural and morphological changes during maturation and aging [1,2]

  • The cardiomyocytes with three and four nuclei have the largest area among cardiomyocytes and are considered the oldest cardiomyocytes as these cells have the highest percentage of apoptosis and the least chance of cellular division [4,5]

  • This study draws on the paradigm that the mature heart, at any given age, contains an admixture of cardiomyocyte precursors, and cardiomyocytes of varying ages [35]

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Summary

Introduction

The heart undergoes structural and morphological changes during maturation and aging [1,2]. The newer model of self-renewal posits that the heart contains a continuum of pre-myocardial and mature-myocardial cell types ranging from resident cardiac progenitor cells, to immature cardiomyocytes, to mature cardiomyocytes containing increasing nucleation in an age-dependent fashion [4,5]. This paradigm of cardiac turnover has gained more credence in the last couple of years, yet controversial issues persist, in humans where the extremely slow turnover of cardiomyocytes creates experimental barriers [6,7]. We evaluated the response to aging and hypertrophy in two mouse strains

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