Journal Article
Animal models to study cardiac regeneration
Weinberger, M. and Riley, P.R.
Record Number:
6254
Year:
2023
Journal:
Nature reviews cardiology
Abstract:
Permanent fibrosis and chronic deterioration of heart function in
patients after myocardial infarction present a major health-care burden
worldwide. In contrast to the restricted potential for cellular and
functional regeneration of the adult mammalian heart, a robust capacity
for cardiac regeneration is seen during the neonatal period in mammals
as well as in the adults of many fish and amphibian species. However,
we lack a complete understanding as to why cardiac regeneration takes
place more efficiently in some species than in others. The capacity of the
heart to regenerate after injury is controlled by a complex network of
cellular and molecular mechanisms that form a regulatory landscape,
either permitting or restricting regeneration. In this Review, we provide
an overview of the diverse array of vertebrates that have been studied
for their cardiac regenerative potential and discuss differential heart
regeneration outcomes in closely related species. Additionally, we
summarize current knowledge about the core mechanisms that regulate
cardiac regeneration across vertebrate species.
Key points
••Cardiac regeneration potential tends to be robust in fish, amphibians
and neonatal mammals, but is restricted in adult mammals; however,
cardiac regeneration potential in several model organisms defies this
trend.
••Cardiac regeneration potential is determined by multiple highly
interconnected processes, including cardiomyocyte proliferation,
cardiac fibrosis, neovascularization, immune response and energy
metabolism.
••Mammalian cardiomyocytes exit the cell cycle postnatally due
to changes in structure and energy metabolism; partial in vivo
reprogramming of adult mammalian cardiomyocytes can increase
their proliferation capacity.
••Fibrosis in the injured heart is both beneficial and detrimental;
altering fibrotic tissue composition and mechanical properties might
improve adult mammalian heart regeneration.
••Rapid neovascularization of the wound is a hallmark of heart
regeneration and is absent in the adult mammalian heart; lymphatic
coronary vessels modify the immune response after myocardial
infarction via immune cell clearance.
••The immune response to cardiac injury consists of multiple phases;
restricting the initial inflammatory phase and promoting the subsequent
reparative phase represents a strategy to improve heart regeneration.
Times Cited:
1
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