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Table 2 Major differences between human iPSC-CMs and adult cardiomyocytes

From: Modeling hypertrophic cardiomyopathy with human cardiomyocytes derived from induced pluripotent stem cells

 

iPSC-CMs

Adult cardiomyocytes

Cellular morphology

Smaller in size, roundish in shape

Larger in size, elongated in shape

Disorganized sarcomeres

Organized sarcomeres

Sarcomeric protein isoforms

Slow skeletal troponin I (ssTnI)

Cardiac troponin I (cTnI)

Higher ratios of α-MHC/β-MHC

Lower ratios of α-MHC/β-MHC

Titin N2BA isoform

Titin N2B isoform

Electrophysiology

Smaller maximum diastolic potential

Larger maximum diastolic potential

Slower upstroke velocity

Faster upstroke velocity

Automaticity in ventricular-like iPSC-CMs

No automaticity in adult ventricular myocytes

Undetectable or significantly smaller IK1

Larger IK1

Calcium handling

Poor calcium handling

Improved calcium handling

No or few T-tubules

Abundant T-tubules

Mitochondrial function

Few and underdeveloped mitochondria

Dense, developed, and well-distributed mitochondria

Metabolic characteristics

Glycolysis as major energy source

Fatty acid β-oxidation as major energy source

  1. IK1 Inward rectifier potassium, iPSC-CMs Induced pluripotent stem cell-derived cardiomyocytes, MHC Myosin heavy chain