Active Heart, Stroke & Blood Cells, Biochemistry & Physiology

Form, Function, Mechanism: How Cellular Physiology Controls Heart Development

In plain English

AI plain-English summary

A beating heart shapes its own developing tissue—the mechanical forces of contraction feed back to switch genes on and off in cardiac progenitor cells. This matters because heart disease involves both structural malformations and changes in how heart cells work, but scientists do not understand how the two are connected. The research targets that gap by studying early heart development, when function first emerges and form is still being built. The researcher will map which genes are active and what physiological signals cardiac progenitors receive as they become different heart cell types, then deliberately disrupt contraction in animal models to see how form changes. Human stem-cell models will recreate the distinct progenitor types found in real embryos, allowing the team to test whether the same mechanisms operate in human tissue. If successful, the work will reveal the molecular pathways that link mechanical activity to gene expression. That knowledge could improve lab-grown heart cells for regenerative medicine and explain why certain genetic or physiological disruptions lead to congenital heart defects. The project is fundamental science—it asks how a living organ builds itself—but understanding that basic logic is a prerequisite for engineering cardiac repair.

View original technical description
Cardiac form and function are inextricably linked. In the heart, disease is associated with changes in both physiology and morphology, although mechanistic insight into this relationship is complicated. Early heart development provides a unique model to explore how the onset of function impacts form. My research programme will use heart development to identify how cellular physiology influences gene expression and cell fate decisions, in order to identify mechanisms with therapeutic potential. To address my research vision, I will temporally define the transcriptional and physiological characteristics of cardiac progenitors as they generate distinct cardiac lineages during the onset of function. I will explore how disrupting function influences form in vivo. Furthermore, and aiming to translate my findings, I will develop in vitro human models, focusing on the generation of distinct cardiac progenitor types identified in the human embryo, enabling me to connect descriptive genomic insight with functional relevance. Functional perturbation experiments will identify pathways which integrate different components of contraction with gene expression, regulating heart development and disease states. My work will enhance models of human heart development and provide insight into the relationship between form and function, aiding in the development of cell-based approaches for cardiac regeneration and heart disease.

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Researchers

Richard Tyser (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Building the first heart
Pathways to the Heart: Exploring how cardiac progenitor heterogeneity arises in human development.
Investigating the mechanosensitive interplays between genetic control and self-organisation during the emergence of cardiac tissue curvature
Understanding Cardiac Progenitors to deliver Regenerative Medicine and Disease Modelling
Early specification and morphogenesis of chamber-specific cardiomyocytes

Original classification

Career Development Award

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