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Published on: May 14, 2019
Heart regeneration: beyond new muscle and vessels
1Department of Physiology, Anatomy and Genetics, British Heart Foundation Oxbridge Centre of Regenerative Medicine, University of Oxford, Sherrington Building, South Parks Road, Oxford OX1 3PT, UK.
Insights
Heart attack recovery requires regenerating heart muscle and blood vessels. This review explores how diverse cell types, beyond muscle and vessel cells, contribute to heart regeneration, suggesting a combinatorial approach.
Area of Science:
- Cardiovascular Research
- Regenerative Medicine
- Cell Biology
Background:
- Heart attacks cause significant loss of heart muscle cells and vasculature, leading to non-functional scar tissue and heart failure.
- Current heart regeneration strategies primarily focus on cardiomyocyte proliferation and angiogenesis.
- Recent advancements reveal extensive cellular heterogeneity and crosstalk within the developing and regenerating heart.
Purpose of the Study:
- To review the roles of non-muscle and non-vessel cell populations in heart development.
- To examine the contribution of diverse cell lineages to cardiac regeneration following injury.
- To highlight the importance of cellular crosstalk in the context of heart repair.
Main Methods:
- Literature review integrating embryological studies, regenerative models, and -omics technologies.
- Focus on the roles of fibroblasts, immune cells, conduction system cells, and nervous system cells.
- Analysis of current evidence for the regenerative potential of these cell populations.
Main Results:
- Fibroblasts, immune cells, conduction system cells, and nervous system cells play crucial roles during heart development.
- These diverse cell populations show potential in contributing to cardiac regeneration after injury.
- Evidence points to significant crosstalk between various cell types in the heart.
Conclusions:
- Heart regeneration research must consider the heterogeneity and interactions of multiple cell types.
- A combinatorial approach involving neurologically, immunologically, and electrically coupled cells is essential for effective heart regeneration.
- Future strategies should move beyond solely targeting cardiomyocytes and angiogenesis to encompass a broader cellular network.
Abstract:
The most striking consequence of a heart attack is the loss of billions of heart muscle cells, alongside damage to the associated vasculature. The lost cardiovascular tissue is replaced by scar formation, which is non-functional and results in pathological remodelling of the heart and ultimately heart failure. It is, therefore, unsurprising that the heart regeneration field has centred efforts to generate new muscle and blood vessels through targeting cardiomyocyte proliferation and angiogenesis following injury. However, combined insights from embryological studies and regenerative models, alongside the adoption of -omics technology, highlight the extensive heterogeneity of cell types within the forming or re-forming heart and the significant crosstalk arising from non-muscle and non-vessel cells. In this review, we focus on the roles of fibroblasts, immune, conduction system, and nervous system cell populations during heart development and we consider the latest evidence supporting a function for these diverse lineages in contributing to regeneration following heart injury. We suggest that the emerging picture of neurologically, immunologically, and electrically coupled cell function calls for a wider-ranging combinatorial approach to heart regeneration.
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