Cooperation between Nodal and FGF signals regulates zebrafish cardiac cell migration and heart morphogenesis.

TitleCooperation between Nodal and FGF signals regulates zebrafish cardiac cell migration and heart morphogenesis.
Publication TypeJournal Article
Year of Publication2024
AuthorsGonzalez V, Grant MG, Suzuki M, Christophers B, Williams JRowland, Burdine RD
JournalbioRxiv
Date Published2024 Jan 06
Abstract

Asymmetric vertebrate heart development is driven by an intricate sequence of morphogenetic cell movements, the coordination of which requires precise interpretation of signaling cues by heart primordia. Here we show that Nodal functions cooperatively with FGF during heart tube formation and asymmetric placement. Both pathways act as migratory stimuli for cardiac progenitor cells (CPCs), but FGF is dispensable for directing heart tube asymmetry, which is governed by Nodal. We further find that Nodal controls CPC migration by inducing left-right asymmetries in the formation of actin-based protrusions in CPCs. Additionally, we define a developmental window in which FGF signals are required for proper heart looping and show cooperativity between FGF and Nodal in this process. We present evidence FGF may promote heart looping through addition of the secondary heart field. Finally, we demonstrate that loss of FGF signaling affects proper development of the atrioventricular canal (AVC), which likely contributes to abnormal chamber morphologies in FGF-deficient hearts. Together, our data shed insight into how the spatiotemporal dynamics of signaling cues regulate the cellular behaviors underlying organ morphogenesis.

DOI10.1101/2024.01.05.574380
Alternate JournalbioRxiv
PubMed ID38260277
PubMed Central IDPMC10802409
Grant ListR01 HD048584 / HD / NICHD NIH HHS / United States
T32 GM007388 / GM / NIGMS NIH HHS / United States

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