Mechanisms and consequences of cell state transitions during heart regeneration
This project aims to uncover the coordinated cellular responses in zebrafish heart regeneration post-injury using single-cell genomics and computational methods to enhance understanding of organ repair mechanisms.
Projectdetails
Introduction
Organs consist of cells with a large diversity of specialized roles. A fundamental question is how these cells mount a coordinated response in space and time to maintain or restore organ function after perturbation. Recent progress in single-cell genomics has generated the opportunity to understand this process on a system-wide scale.
Model System
We will use the adult zebrafish heart as a powerful model system to dissect how regeneration after injury is orchestrated by the activation response of multiple different cell types.
Research Objectives
To understand how activated cell states are generated and how they interact to drive the regenerative process, we will:
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Define which cell types react to injury and measure their activation profiles.
We will develop new experimental and computational strategies for measuring cell states, including a “molecular time machine” that records the past transcriptome of single cells based on RNA labeling. -
Discover the mechanisms that induce cell state activation upon injury.
We will combine single-cell transcriptomics and open chromatin profiling to infer gene regulatory networks, and we will use functional experiments to validate the identified pathways. -
Reveal pro-regenerative cell types and understand their role in the regenerative process.
We will combine spatial transcriptomics and computational analysis to identify putative cellular interactions, and we will use targeted cell type depletion and signaling inhibition to confirm our findings.
Expected Outcomes
In this manner, we will provide the first comprehensive view of how cell type activation leads to a synergistic response in organ regeneration. Furthermore, the approaches and concepts developed in this project will be applicable to other systems in regeneration and beyond.
Future Implications
Finally, understanding the underlying mechanisms in zebrafish, the preeminent model for heart regeneration, will open up exciting avenues for awakening the dormant regenerative potential of the human heart.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 2.000.000 |
Totale projectbegroting | € 2.000.000 |
Tijdlijn
Startdatum | 1-3-2023 |
Einddatum | 29-2-2028 |
Subsidiejaar | 2023 |
Partners & Locaties
Projectpartners
- MAX DELBRUECK CENTRUM FUER MOLEKULARE MEDIZIN IN DER HELMHOLTZ-GEMEINSCHAFT (MDC)penvoerder
Land(en)
Vergelijkbare projecten binnen European Research Council
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Tight junctions and tissue mechanics as sensors and executers of heart regeneration
This project aims to understand salamander regeneration by integrating gene editing, imaging, and mechanical analysis to explore tight junctions' role in cellular responses and regeneration control.
Mechanisms of liver regeneration and disease across scales; from molecules to cells and tissue
This project aims to uncover liver regeneration mechanisms and disease pathways to develop complex organoids for studying tissue repair and disease principles.
Collective Regulation of Cell Decisions
This project aims to explore how collective tissue properties influence cell decisions in zebrafish by manipulating cell parameters to engineer tissue characteristics and uncover developmental mechanisms.
Programming the EPIcardium to CURE broken hearts
EPICURE aims to decode human epicardial development and regeneration using pluripotent stem cell-derived epicardioids, enhancing insights for cardiac repair through advanced imaging and CRISPR techniques.
The transcriptional regulation of cardiomyocyte polyploidization and its relevance in cardiac regeneration
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