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Neural signaling contributes to heart formation and growth in the invertebrate chordate, Ciona robusta
Neural signaling contributes to heart formation and growth in the invertebrate chordate, Ciona robusta
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Neural signaling contributes to heart formation and growth in the invertebrate chordate, Ciona robusta
Neural signaling contributes to heart formation and growth in the invertebrate chordate, Ciona robusta

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Neural signaling contributes to heart formation and growth in the invertebrate chordate, Ciona robusta
Neural signaling contributes to heart formation and growth in the invertebrate chordate, Ciona robusta
Journal Article

Neural signaling contributes to heart formation and growth in the invertebrate chordate, Ciona robusta

2026
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Overview
Neurons contribute to the complex interplay of signals that mediate heart development and homeostasis. Although a limited set of studies suggest that neuronal peptides impact vertebrate heart growth, the specific contributions of these peptides to cardiomyocyte progenitor differentiation or proliferation have not been elucidated. Here, we show that the neuropeptide tachykinin along with canonical Wnt signaling regulate cardiomyocyte progenitor proliferation in the chordate model Ciona robusta . In C. robusta , the heart continues to grow throughout adulthood and classic histological studies indicate that a line of undifferentiated cells may serve as a reserve progenitor lineage. We found that this line of cardiomyocyte progenitors consists of distinct distal and midline populations. Our analysis indicates that distal progenitors divide asymmetrically to produce distal and midline daughters while midline progenitors divide asymmetrically to produce myocardial precursors. Through single-cell RNA sequencing (scRNA-seq) of adult C. robusta hearts, we delineated the cardiomyocyte progenitor expression profile. Based on this data, we investigated the role of Wnt signaling in cardiomyocyte progenitor proliferation and found that canonical Wnt signaling is required to suppress excessive progenitor proliferation. The scRNA-seq data also identified a number of presumptive cardiac neural-like cells. Strikingly, we found that a subset of these neuronal cells appears to innervate the distal cardiomyocyte progenitors. Based on tachykinin receptor expression in these neural-like cells, we blocked tachykinin signaling using pharmacological inhibitors and found that this led to reduced proliferation in the distal progenitor pool. Through targeted CRISPR-Cas9 knockdown, we then demonstrated that both extrinsic tachykinin and intrinsic cardiac tachykinin receptors are required for formation of the myocardial heart tube. This work provides valuable insights regarding the deployment of neural signals to regulate organ growth in response to environmental or homeostatic inputs.