HMN 2026: How Lab-grown heart tissue beats on its own as sensors track force in real time

Lab-grown, 'living' heart tissues produced through 3D bioprinting
Tissue formation and compaction. Credit: Small (2025). DOI: 10.1002/smll.202504493

Scientists at Université de Montréal and its affiliated Centre de recherche Azrieli du CHU Sainte-Justine have made a major advance in their research into cardiovascular disease: They’ve created functional, three-dimensional heart tissue that can beat autonomously in vitro. The tissue incorporates micro-sensors that make it possible to do finely tuned, real-time analysis of its contractile properties. This advance marks an important step forward for modeling human cardiac diseases and conducting preclinical drug testing.

‘Hearts on a chip’

Described as “hearts on a chip,” the engineered heart tissues are produced through 3D bioprinting with a bio-ink developed in Savoji’s laboratory using patient-harvested stem cells, enabling personalized human heart models to be created.

Led by UdeM pharmacology and physiology professor Houman Savoji at his laboratory at CHU Sainte-Justine, along with UdeM Ph.D. student Ali Mousavi, the research is detailed in a study published in the journal Small. An initial version of the technology was published two years ago, in a study in Applied Materials Today.

The new study marks a major step forward: The direct integration of ultra-soft, biocompatible and fluorescent mechanical sensors within the heart tissue itself. These sensors allow for unprecedented precision in measuring the contractile forces generated at both the cellular level and across the entire tissue, using non-destructive optical methods.

Lab-grown, 'living' heart tissues produced through 3D bioprinting
A schematic representation of the study describes tissue formation by encapsulating neonatal rat cardiac cells within a fibrin/Geltrex hydrogel mixture. Credit: Small (2025). DOI: 10.1002/smll.202504493

Unlike existing heart-on-a-chip platforms—often limited in their ability to capture localized forces within dynamic 3D tissues—this approach delivers high-resolution, real-time, mechanical data. It therefore more accurately reflects the complexity of the human myocardium, the muscle responsible for cardiac contraction.

The researchers also measured calcium activity within the tissues, visualizing in real time the calcium waves that trigger each heartbeat. They further demonstrated that their hearts on a chip respond to drugs just like real cardiac tissues, confirming the model’s sensitivity for pharmacological screening.

In previous research, the researchers created hearts on a chip, ring-shaped devices 3D-printed using a bio-ink containing the patient’s own stem cells.

Next up: Models for more diseases

The team is now working to develop models of cardiovascular diseases such as dilated cardiomyopathy and some arrhythmias, by comparing tissues derived from the cells of patients living with these conditions to tissues generated from those of healthy individuals.

Ultimately, this technology could enable the modeling of a wide range of cardiac disorders and the precise assessment of potential therapies, the researchers say.

“The ability to observe the tissue’s response to different compounds in real time represents a major advantage for preclinical development and translational research,” said Mousavi, the study’s first author. “This allows us to test directly on a patient’s own cells, without any invasive procedures.”

Savoji, the study’s principal investigator, added, “This breakthrough brings us even closer to true precision health, by giving us the ability to identify the most effective medication for each person before treatment is even administered.”

Publication details

Ali Mousavi et al, Heart?On?a?Chip with Integrated Ultrasoft Mechanosensors for Continuous Measurement of Cell? and Tissue?Scale Contractile Stresses, Small (2025). DOI: 10.1002/smll.202504493

Journal information:
Small


Key medical concepts

3D BioprintingsCardiomyopathy, Dilated

Clinical categories

CardiologyClinical pharmacology


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