ErbB2 is required for cardiomyocyte proliferation in murine neonatal hearts

• Cardiac ErbB2 exhibited a steep decrease in expression from embryonic to postnatal stage.
• ErbB2 is required for neonatal cardiomyocyte proliferation in murine.
• ErbB2 conditional knockout heart exhibited an upregulation of negative cell cycle regulators.

It has been long recognized that the mammalian heart loses its proliferative capacity soon after birth, yet, the molecular basis of this loss of cardiac proliferation postnatally is largely unknown. In this study, we found that cardiac ErbB2, a member of the epidermal growth factor receptor family, exhibits a rapid and dramatic decline in expression at the neonatal stage. We further demonstrate that conditional ablation of ErbB2 in the ventricular myocardium results in upregulation of negative cell cycle regulators and a significant reduction in cardiomyocyte proliferation during the narrow neonatal proliferative time window. Together, our data reveal a positive correlation between the expression levels of ErbB2 with neonatal cardiomyocyte proliferation and suggest that reduction in cardiac ErbB2 expression may contribute to the loss of postnatal cardiomyocyte proliferative capacity.