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Cooperation between Nodal and FGF signals regulates zebrafish cardiac cell migration and heart morphogenesis.
Gonzalez, Vanessa; Grant, Meagan G; Suzuki, Makoto; Christophers, Briana; Rowland Williams, Jessica; Burdine, Rebecca D.
Afiliação
  • Gonzalez V; Department of Molecular Biology, Princeton University, Princeton, New Jersey, USA, 08544.
  • Grant MG; Department of Molecular Biology, Princeton University, Princeton, New Jersey, USA, 08544.
  • Suzuki M; Amphibian Research Center, Graduate School of Integrated Sciences for Life, Hiroshima University, Higashihiroshima, Hiroshima, Japan, 739-8526.
  • Christophers B; Department of Molecular Biology, Princeton University, Princeton, New Jersey, USA, 08544.
  • Rowland Williams J; Department of Molecular Biology, Princeton University, Princeton, New Jersey, USA, 08544.
  • Burdine RD; Current affiliation: National Institute for Student Success, at Georgia State University, Atlanta, GA 30303.
bioRxiv ; 2024 Jan 06.
Article em En | MEDLINE | ID: mdl-38260277
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article