A tissue-engineered scale model of the heart ventricle.
Luke A MacQueenSean P SheehyChristophe O ChantreJohn F ZimmermanFrancesco S PasqualiniXujie LiuJosue A GossPatrick H CampbellGrant M GonzalezSung-Jin ParkAndrew K CapulliJohn P FerrierT Fettah KosarLakshminarayanan MahadevanWilliam T PuKevin Kit ParkerPublished in: Nature biomedical engineering (2018)
Laboratory studies of the heart use cell and tissue cultures to dissect heart function yet rely on animal models to measure pressure and volume dynamics. Here, we report tissue-engineered scale models of the human left ventricle, made of nanofibrous scaffolds that promote native-like anisotropic myocardial tissue genesis and chamber-level contractile function. Incorporating neonatal rat ventricular myocytes or cardiomyocytes derived from human induced pluripotent stem cells, the tissue-engineered ventricles have a diastolic chamber volume of ~500 µl (comparable to that of the native rat ventricle and approximately 1/250 the size of the human ventricle), and ejection fractions and contractile work 50-250 times smaller and 104-108 times smaller than the corresponding values for rodent and human ventricles, respectively. We also measured tissue coverage and alignment, calcium-transient propagation and pressure-volume loops in the presence or absence of test compounds. Moreover, we describe an instrumented bioreactor with ventricular-assist capabilities, and provide a proof-of-concept disease model of structural arrhythmia. The model ventricles can be evaluated with the same assays used in animal models and in clinical settings.
Keyphrases
- induced pluripotent stem cells
- endothelial cells
- heart failure
- left ventricular
- pulmonary hypertension
- pulmonary artery
- mitral valve
- blood brain barrier
- blood pressure
- congenital heart disease
- pulmonary arterial hypertension
- brain injury
- mesenchymal stem cells
- bone marrow
- tissue engineering
- coronary artery
- health insurance
- subarachnoid hemorrhage
- smooth muscle