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.

Subsidie
€ 2.000.000
2023

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:

  1. 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.

  2. 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.

  3. 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

Startdatum1-3-2023
Einddatum29-2-2028
Subsidiejaar2023

Partners & Locaties

Projectpartners

  • MAX DELBRUECK CENTRUM FUER MOLEKULARE MEDIZIN IN DER HELMHOLTZ-GEMEINSCHAFT (MDC)penvoerder

Land(en)

Germany

Vergelijkbare projecten binnen European Research Council

ERC Starting...

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.

€ 2.318.778
ERC Consolid...

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.

€ 1.999.980
ERC Starting...

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.

€ 2.486.429
ERC Advanced...

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.

€ 2.499.999
ERC Advanced...

The transcriptional regulation of cardiomyocyte polyploidization and its relevance in cardiac regeneration

REACTIVA aims to promote heart regeneration by reactivating adult diploid cardiomyocytes through a newly identified regulatory network and inhibiting a specific transcription factor.

€ 2.500.000