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Updated: Dec 19, 2025

Model of Ischemic Heart Disease and Video-Based Comparison of Cardiomyocyte Contraction Using hiPSC-Derived Cardiomyocytes
Published on: May 5, 2020
Human iPSC-Derived Cardiomyocytes are Susceptible to SARS-CoV-2 Infection
Insights
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) directly infects human heart cells, causing cell death and stopping heart cell beating. This research establishes a model for studying COVID-19
Area of Science:
- Cardiology
- Virology
- Cell Biology
Background:
- COVID-19, caused by SARS-CoV-2, presents with respiratory symptoms but frequently involves cardiac complications.
- The direct effects of SARS-CoV-2 on heart muscle cells (cardiomyocytes) remain unclear, despite potential impacts from systemic inflammation and ischemia.
Approach:
- Utilized human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) as an in vitro model.
- Employed microscopy and immunofluorescence to visualize SARS-CoV-2 entry, replication, and localization within hiPSC-CMs.
Key Points:
- SARS-CoV-2 successfully infected hiPSC-CMs, replicating within the cytoplasm.
- Infection led to observable viral cytopathic effects, including apoptosis and cessation of beating in hiPSC-CMs after 72 hours.
- Demonstrated SARS-CoV-2's ability to infect cardiomyocytes directly.
Conclusions:
- SARS-CoV-2 can directly infect and harm human cardiomyocytes in vitro.
- The hiPSC-CM model provides a platform for investigating SARS-CoV-2 cardiac infection mechanisms.
- This model may facilitate the development and screening of cardiac-specific antiviral therapies for COVID-19.
Abstract:
Coronavirus disease 2019 (COVID-19) is a viral pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). COVID-19 is predominantly defined by respiratory symptoms, but cardiac complications including arrhythmias, heart failure, and viral myocarditis are also prevalent. Although the systemic ischemic and inflammatory responses caused by COVID-19 can detrimentally affect cardiac function, the direct impact of SARS-CoV-2 infection on human cardiomyocytes is not well-understood. We used human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) as a model system to examine the mechanisms of cardiomyocyte-specific infection by SARS-CoV-2. Microscopy and immunofluorescence demonstrated that SARS-CoV-2 can enter and replicate within hiPSC-CMs, localizing at perinuclear locations within the cytoplasm. Viral cytopathic effect induced hiPSC-CM apoptosis and cessation of beating after 72 hours of infection. These studies show that SARS-CoV-2 can infect hiPSC-CMs in vitro , establishing a model for elucidating the mechanisms of infection and potentially a cardiac-specific antiviral drug screening platform.
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