Regulated HSPG Signaling Directs Epicardial Behavior to Support Cardiac Formation
TL;DR
It is shown that epicardial SULF1 dynamically regulates HSPG sulfation to fine-tune the magnitude and duration of signaling to impact cell fate and cardiac morphogenesis, highlighting, for the first time, essential fine-tuning of HSPG-dependent signaling to modulate key processes in heart formation.
Abstract
Background
Pathways controlling cardiac cell behavior share a common dependency on heparan sulfate proteoglycans (HSPGs), which tightly regulate signaling at extracellular locations. This signaling is essential for cardiac development, yet how HSPGs are regulated in the forming heart is unknown. The epicardium is a rich source of HSPG-dependent signaling and cellular progenitors. We hypothesized that extracellular heparan sulfate modifiers, 6-O-endosulfatases, orchestrate progenitor cell behavior to support cardiogenesis.
Methods
We used single-cell RNA sequencing, microscopy, and flow cytometry–based single-molecule RNA in situ hybridization (ISH) to systematically profile 6-O-endosulfatases and target HSPGs in the embryonic mouse heart. Subsequently, we utilized knockout and knockdown models that identified gene associations and a role for the main epicardial 6-O-endosulfatase isoform, Sulfatase (Sulf)1. Transcriptional regulation of Sulf1 was assessed using assay for transposase-accessible chromatin (ATAC) and Cleavage Under Targets and Release Using Nuclease (CUT&RUN) with sequencing, luciferase assays, and siRNA, and the impact on epicardial cell behavior was confirmed in vivo and using in vitro functional assays.
Results
Despite identical function, we find that Sulf1 is expressed in the embryonic epicardium, while Sulfatase (Sulf)2 is expressed broadly throughout the myocardium. We show that epicardial SULF1 dynamically regulates HSPG sulfation to fine-tune the magnitude and duration of signaling to impact cell fate and cardiac morphogenesis. Single-cell genomics and lineage tracing studies reveal Sulf1 to be strongly coexpressed with key transcriptional regulator Wt1 (Wilms tumor 1) in the epicardium, with reduction of both coinciding with epithelial-to-mesenchymal transition and quiescence. CUT&RUN-seq revealed transcriptional control of Sulf1 by WT1, which directly impacts essential HSPG-dependent downstream signaling. Ligand-receptor interaction predictions and functional assays indicated that FGF (fibroblast growth factor)-2 and TGF-β (transforming growth factor β)–driven processes were governed by this regulatory interaction.
Conclusions
Our study highlights, for the first time, essential fine-tuning of HSPG-dependent signaling to modulate key processes in heart formation, offering potential insights for therapeutically targeting congenital heart disease and enhancing epicardial proregenerative behaviors.