Context Dependent Sulf1/Sulf2 Functional Divergence in Endothelial Cell Activity

• Published in: International journal of molecular sciences Vol. 23; no. 7; p. 3769
• Main Authors: Justo, Tiago, Smart, Nicola, Dhoot, Gurtej K
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 29.03.2022; MDPI
• Subjects: Alternative splicing; Angiogenesis; Blood vessels; Cardiomyocytes; Cell lines; Cell membranes; Divergence; Endothelial cells; Endothelial Cells - metabolism; Enzymes; Extracellular matrix; Feedback; Growth factors; Heparan sulfate; Heparan Sulfate Proteoglycans; Hypoxia; Kinases; Microvasculature; mRNA; Overexpression; Phenotypes; Proteoglycans; Roles; Splicing; Sulf1; Sulf2; Sulfation; Sulfotransferases - genetics; Sulfotransferases - metabolism; TGFβ cell signalling; Transforming Growth Factor beta; Transforming growth factor-b; Vascular endothelial growth factor; Vascular Endothelial Growth Factor A - genetics; VEGF cell signalling; TGFβ cell signalling; VEGF cell signalling; Sulf1; angiogenesis; Sulf2
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms23073769

Signalling activities are tightly regulated to control cellular responses. Heparan sulfate proteoglycans (HSPGs) at the cell membrane and extracellular matrix regulate ligand availability and interaction with a range of key receptors. SULF1 and SULF2 enzymes modify HSPG sulfation by removing 6-O sulfates to regulate cell signalling but are considered functionally identical. Our in vitro mRNA and protein analyses of two diverse human endothelial cell lines, however, highlight their markedly distinct regulatory roles of maintaining specific HSPG sulfation patterns through feedback regulation of HS 6-O transferase (HS6ST) activities and highly divergent roles in vascular endothelial growth factor (VEGF) and Transforming growth factor β (TGFβ) cell signalling activities. Unlike Sulf2, Sulf1 over-expression in dermal microvascular HMec1 cells promotes TGFβ and VEGF cell signalling by simultaneously upregulating HS6ST1 activity. In contrast, Sulf1 over-expression in venous ea926 cells has the opposite effect as it attenuates both TGFβ and VEGF signalling while Sulf2 over-expression maintains the control phenotype. Exposure of these cells to VEGF-A, TGFβ1, and their inhibitors further highlights their endothelial cell type-specific responses and integral growth factor interactions to regulate cell signalling and selective feedback regulation of HSPG sulfation that additionally exploits alternative Sulf2 RNA-splicing to regulate net VEGF-A and TGFβ cell signalling activities.