Key result
Brain, lymphoid, and gut signals drive heart development, homeostasis, and regeneration following ischemic injury.
Why the study?
Heart development, homeostasis, and regenerative capability rely on multi-organ collaborative signals beyond cardiac-intrinsic factors, warranting an overview of inter-organ communication and therapeutic potential.
Heart development and regeneration rely on complex inter-organ communication, suggesting potential therapeutic approaches targeting systemic modulatory signals for cardiac repair.
Inter-organ signals merit exploration as therapeutic targets; leaves open validation in prospective human studies before any clinical adoption.
Development of the heart, from early morphogenesis to functional maturation, as well as maintenance of its homeostasis are tasks requiring collaborative efforts of cardiac tissue and different extra-cardiac organ systems. The brain, lymphoid organs, and gut are among the interaction partners that can communicate with the heart through a wide array of paracrine signals acting at local or systemic level. Disturbance of cardiac homeostasis following ischemic injury also needs immediate response from these distant organs. Our hearts replace dead muscles with non-contractile fibrotic scars. We have learned from animal models capable of scarless repair that regenerative capability of the heart does not depend only on competency of the myocardium and cardiac-intrinsic factors but also on long-range molecular signals originating in other parts of the body. Here, we provide an overview of inter-organ signals that take part in development and regeneration of the heart. We highlight recent findings and remaining questions. Finally, we discuss the potential of inter-organ modulatory approaches for possible therapeutic use.
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Filosa et al. (2021) conducted a review in Heart development and regeneration. Inter-organ signals from the brain, lymphoid organs, and gut play a crucial role in heart development, homeostasis, and regeneration following ischemic injury.
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