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.

PubMed

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.
Abstract

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