Key result
MYH7 E848G variant cuts twitch force ~38% and increases p53-independent apoptosis in an HCM model.
Why the study?
Missense mutations in MYH7 commonly cause hypertrophic cardiomyopathy, but the underlying molecular mechanisms remain unclear.
Absolute Event Rate: 147% vs 238.2%
p-value: p=<0.05
In a stem cell model of MYH7 E848G hypertrophic cardiomyopathy, contractile dysfunction and apoptosis are p53-independent, suggesting alternative cell death pathways should be targeted.
p53-independent apoptosis may drive MYH7 HCM phenotypes in stem cell models; leaves open alternative pathways for targeted therapies pending human validation.
Missense mutations in myosin heavy chain 7 (MYH7) are a common cause of hypertrophic cardiomyopathy (HCM), but the molecular mechanisms underlying MYH7-based HCM remain unclear. In this work, we generated cardiomyocytes derived from isogenic human induced pluripotent stem cells to model the heterozygous pathogenic MYH7 missense variant, E848G, which is associated with left ventricular hypertrophy and adult-onset systolic dysfunction. MYH7E848G/+ increased cardiomyocyte size and reduced the maximum twitch forces of engineered heart tissue, consistent with the systolic dysfunction in MYH7E848G/+ HCM patients. Interestingly, MYH7E848G/+ cardiomyocytes more frequently underwent apoptosis that was associated with increased p53 activity relative to controls. However, genetic ablation of TP53 did not rescue cardiomyocyte survival or restore engineered heart tissue twitch force, indicating MYH7E848G/+ cardiomyocyte apoptosis and contractile dysfunction are p53-independent. Overall, our findings suggest that cardiomyocyte apoptosis is associated with the MYH7E848G/+ HCM phenotype in vitro and that future efforts to target p53-independent cell death pathways may be beneficial for the treatment of HCM patients with systolic dysfunction.
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Loiben et al. (2023) studied Hypertrophic cardiomyopathy. MYH7 E848G mutation vs. Wild-type (MYH7 WT/WT) hiPSC-CMs was evaluated on Maximum twitch force of engineered heart tissues at 3 weeks (p=<0.05). The MYH7 E848G variant increased cardiomyocyte size, reduced maximum twitch force, and increased p53-independent apoptosis compared to wild-type controls in a stem cell model of hypertrophic cardiomyopathy.
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