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Biology subjects

Garric, L.

Publications and source records attributed to Garric, L..

2 recordsLinked to original sources

Reciprocal repression between Isl1 and Nkx2-5 defines the zebrafish embryonic cardiac pacemaker domain

The cardiac pacemaker initiates each heartbeat and is essential for normal cardiac function. Although the gene regulatory network controlling pacemaker development has been extensively studied in mammals, it remains unclear whether the same regulatory hierarchy governs pacemaker development in other vertebrates. Here, we combined high-speed optical mapping with genetic analysis to define the gene regulatory network that establishes and maintains pacemaker identity in the zebrafish embryo. We show that the LIM-homeodomain transcription factor Isl1 is essential for maintaining pacemaker identity of venous pole cardiomyocytes. Loss of Isl1 causes pacemaker cells to acquire chamber-like characteristics through ectopic nkx2-5 expression, resulting in loss of a dominant pacemaker site and severe bradyarrhythmia. Reducing Nkx2-5 activity largely restores regular rhythm despite persistent loss of other Isl1-dependent markers, indicating that inappropriate Nkx2-5 activity contributes substantially to the electrophysiological defects in isl1 mutants. In contrast, genetic disruption of shox2 does not impair embryonic pacemaker development or alter isl1 expression, suggesting that Shox2 is not an essential component of the zebrafish pacemaker gene regulatory network. Together, our findings establish a zebrafish-specific transcriptional hierarchy in which Isl1 safeguards pacemaker identity by restricting Nkx2-5 independently of Shox2. These results show that a conserved boundary between pacemaker and chamber myocardium can be maintained by distinct upstream factors during vertebrate heart development.

developmental biology↗

A metabolic switch from OXPHOS to glycolysis is essential for cardiomyocyte proliferation in the regenerating heart

The capacity to regenerate damaged tissues, such as the heart, various enormously amongst species. While heart regeneration is generally very low in mammals 1-3, it can regenerate efficiently in certain amphibian and fish species 4,5. Zebrafish has been used extensively to study heart regeneration, resulting in the identification of proliferating cardiomyocytes that drive this process 5-7. However, mechanisms that drive cardiomyocyte proliferation are largely unknown. Here, using a single-cell mRNA-sequencing approach, we find a transcriptionally distinct population of dedifferentiated and proliferating cardiomyocytes in regenerating zebrafish hearts. While adult cardiomyocytes are known to rely on mitochondrial oxidative phosphorylation (OXPHOS) for energy production, these proliferating cardiomyocytes show reduced mitochondrial gene expression and decreased OXPHOS activity. Strikingly, we find that genes encoding rate-limiting enzymes of the glycolysis pathway are induced in the proliferating cardiomyocytes, and inhibiting glycolysis impairs cardiomyocyte cell cycle reentry. Mechanistically, glycolytic gene expression is induced by Nrg1/Erbb2 signaling, and this is conserved in a mouse model of enhanced regeneration. Moreover, inhibiting glycolysis in murine cardiomyocytes abrogates the mitogenic effects of Nrg1/ErbB2 signaling. Together these results reveal a conserved mechanism in which cardiomyocytes undergo metabolic reprogramming by activating glycolysis, which is essential for cell cycle reentry and heart regeneration. This could ultimately help develop therapeutic interventions that promote the regenerative capacity of the mammalian heart.

cell biology↗