Related Experiment Video
Updated: Jan 4, 2026

Model of Ischemic Heart Disease and Video-Based Comparison of Cardiomyocyte Contraction Using hiPSC-Derived Cardiomyocytes
Published on: May 5, 2020
High-Throughput Phenotyping Toolkit for Characterizing Cellular Models of Hypertrophic Cardiomyopathy In Vitro
Diogo Mosqueira1, Katarzyna Lis-Slimak1, Chris Denning1
1Department of Stem Cell Biology, Centre of Biomolecular Sciences, University of Nottingham, Nottingham NG7 2RD, UK.
Insights
New high-throughput protocols enable unbiased cellular analysis of hypertrophic cardiomyopathy (HCM) in vitro. These methods improve understanding of HCM progression and aid drug screening for cardiac disease modeling.
Area of Science:
- Cardiovascular Research
- Cell Biology
- Biomedical Engineering
Background:
- Hypertrophic cardiomyopathy (HCM) is a complex cardiovascular disease with diverse clinical and molecular features.
- Existing disease models often yield contradictory results due to technical limitations.
- There is a need for refined, unbiased tools to study HCM pathology and progression.
Purpose of the Study:
- To present three simple, high-throughput protocols for phenotyping cellular models of HCM in vitro.
- To minimize technical artifacts in the investigation of hypertrophic cardiomyopathy.
- To provide accessible tools for understanding HCM and facilitating drug screening.
Main Methods:
- Cell volume measurement by flow cytometry to assess hypertrophy.
- High-content imaging for analyzing hypertrophic markers, multinucleation, and sarcomeric disarray.
- Seahorse™ platform analysis for mitochondrial respiration and content.
Main Results:
- The described protocols offer straightforward evaluation of molecular and functional HCM parameters in vitro.
- These methods are designed for high-throughput analysis with minimized technical artifacts.
- The protocols are applicable to various cellular models beyond HCM.
Conclusions:
- These protocols provide essential tools for advancing the understanding of hypertrophic cardiomyopathy.
- The methods support high-throughput drug screening for cardiac disease modeling.
- The approaches are broadly applicable to other cellular models investigating similar biological changes.
Abstract:
Hypertrophic cardiomyopathy (HCM) is a prevalent and complex cardiovascular disease characterised by multifarious hallmarks, a heterogeneous set of clinical manifestations, and several molecular mechanisms. Various disease models have been developed to study this condition, but they often show contradictory results, due to technical constraints and/or model limitations. Therefore, new tools are needed to better investigate pathological features in an unbiased and technically refined approach, towards improving understanding of disease progression. Herein, we describe three simple protocols to phenotype cellular models of HCM in vitro, in a high-throughput manner where technical artefacts are minimized. These are aimed at investigating: (1) Hypertrophy, by measuring cell volume by flow cytometry; (2) HCM molecular features, through the analysis of a hypertrophic marker, multinucleation, and sarcomeric disarray by high-content imaging; and (3) mitochondrial respiration and content via the Seahorse™ platform. Collectively, these protocols comprise straightforward tools to evaluate molecular and functional parameters of HCM phenotypes in cardiomyocytes in vitro. These facilitate greater understanding of HCM and high-throughput drug screening approaches and are accessible to all researchers of cardiac disease modelling. Whilst HCM is used as an exemplar, the approaches described are applicable to other cellular models where the investigation of identical biological changes is paramount.
More Related Videos
14:03High-Throughput Cardiotoxicity Screening Using Mature Human Induced Pluripotent Stem Cell-Derived Cardiomyocyte Monolayers
Published on: March 24, 2023
10:37Fabrication of 3D Cardiac Microtissue Arrays using Human iPSC-Derived Cardiomyocytes, Cardiac Fibroblasts, and Endothelial Cells
Published on: March 14, 2021