Dissecting mechanisms of chamber-specific cardiac differentiation and its perturbation following retinoic acid exposure

David M. Gonzalez, Nadine Schrode, Tasneem A.M. Ebrahim, Nicolas Broguiere, Giuliana Rossi, Lika Drakhlis, Robert Zweigerdt, Matthias P. Lutolf, Kristin G. Beaumont, Robert Sebra, Nicole C. Dubois

Research output: Contribution to journalArticlepeer-review

Abstract

The specification of distinct cardiac lineages occurs before chamber formation and acquisition of bona fide atrial or ventricular identity. However, the mechanisms underlying these early specification events remain poorly understood. Here, we performed single cell analysis at the murine cardiac crescent, primitive heart tube and heart tube stages to uncover the transcriptional mechanisms underlying formation of atrial and ventricular cells. We find that progression towards differentiated cardiomyocytes occurs primarily based on heart field progenitor identity, and that progenitors contribute to ventricular or atrial identity through distinct differentiation mechanisms. We identify new candidate markers that define such differentiation processes and examine their expression dynamics using computational lineage trajectory methods. We further show that exposure to exogenous retinoic acid causes defects in ventricular chamber size, dysregulation in FGF signaling and a shunt in differentiation towards orthogonal lineages. Retinoic acid also causes defects in cell-cycle exit resulting in formation of hypomorphic ventricles. Collectively, our data identify, at a single cell level, distinct lineage trajectories during cardiac specification and differentiation, and the precise effects of manipulating cardiac progenitor patterning via retinoic acid signaling.

Original languageEnglish
JournalDevelopment (Cambridge)
Volume149
Issue number13
DOIs
StatePublished - 1 Jul 2022

Keywords

  • Cardiac development
  • Cardiac organoid
  • Cardiac progenitor
  • Mouse
  • Retinoic acid
  • Single cell RNA-sequencing

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