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Updated: Aug 3, 2026

Model of Ischemic Heart Disease and Video-Based Comparison of Cardiomyocyte Contraction Using hiPSC-Derived Cardiomyocytes
Published on: May 5, 2020
SARS-CoV-2-infected hiPSC-derived cardiomyocytes reveal dynamic changes in the COVID-19 hearts
Xiao Li1,2, Hengrui Hu3, Wanlin Liu2
1Stem Cell and Regenerative Medicine Lab, Department of Medical Science Research Center, Institute of Clinical Medicine, State Key Laboratory of Complex Severe and Rare Diseases, Translational Medicine Center, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
Insights
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection impacts heart cell metabolism and DNA repair. Understanding these changes in cardiomyocytes is key for developing targeted COVID-19 treatments.
Area of Science:
- Cardiology
- Virology
- Molecular Biology
Background:
- The COVID-19 pandemic presents significant societal and medical challenges.
- Heart failure is a common reason for COVID-19 patient readmission.
- Understanding long-term COVID-19 effects on the heart is crucial.
Purpose of the Study:
- To develop an in vitro model of SARS-CoV-2 infection using human induced pluripotent stem cell (hiPSC)-derived cardiomyocytes.
- To investigate dynamic proteomic changes in cardiomyocytes post-SARS-CoV-2 infection.
- To identify potential therapeutic targets for COVID-19 related cardiac complications.
Main Methods:
- Utilized hiPSC-derived cardiomyocytes to model SARS-CoV-2 infection.
- Employed time-series proteomics to analyze protein expression changes.
- Integrated proteomics data with virus-host interaction network analysis.
Main Results:
- SARS-CoV-2 infection significantly alters lipid and energy metabolism in early stages.
- DNA repair mechanisms in cardiomyocytes are affected during later stages of infection.
- Distinct protein expression patterns characterize different timepoints of the simulated COVID-19 course.
Conclusions:
- Early detection and stage-specific personalized treatment are vital for managing COVID-19.
- Proteomics and network analysis identified potential drug targets for COVID-19.
- This study provides insights into the molecular mechanisms of cardiac dysfunction in COVID-19.
Background:
The ongoing coronavirus disease 2019 (COVID-19) pandemic has had an enormous impact on our societies. Moreover, the disease's extensive and sustained symptoms are now becoming a nonnegligible medical challenge. In this respect, data indicate that heart failure is one of the most common readmission diagnoses among COVID-19 patients.
Methods:
In this study, we used human induced pluripotent stem cell (hiPSC)-derived cardiomyocytes to develop an in vitro model of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and studied the dynamic changes occurring in cardiomyocytes after SARS-CoV-2 infection.
Results:
To this end, we have created an effective time series SARS-CoV-2 infection model exhibiting different functional patterns of up- and downregulated proteins, and demonstrating that SARS-CoV-2 mainly affects (i) the lipid and the energy metabolism of hiPSC-derived cardiomyocytes during the early infection stage, and (ii) the DNA repair ability of cardiomyocytes during the late infection stage. By analyzing the proteome changes occurring at different infection timepoints, we were able to observe that the simulated disease (COVID-19) course developed rapidly, and that each of the studied timepoints was characterized by a distinct protein expression pattern.
Conclusions:
Our findings highlight the importance of early detection and personalized treatment based on the disease stage. Finally, by combing the proteomics data with virus-host interaction network analysis, we were able to identify several potential drug targets for the disease.
Related Concept Videos
Myocarditis I: Introduction
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy
Coronavirus

