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Effect of heparan sulfate cleavage on homeostatic gene expression in microvascular endothelial cells

GSE260628 Homo sapiens Expression profiling by high throughput sequencing 4 samples Submitted 2024/08/14 Platform GPL21697
Summary
Heparan sulfate (HS) in the vascular endothelial glycocalyx (eGC) is a critical regulator of blood vessel homeostasis. Trauma results in HS shedding from the eGC, but the impact of HS shedding on mechanisms of vascular injury and repair has not been evaluated. The objective of this work was to characterize the effect of eGC HS shedding on the transcriptional landscape of vascular endothelial cells. In vitro work was performed using flow conditioned primary human lung microvascular ECs treated with vehicle or heparin lyase III to simulate human heparanase activity. Bulk RNA sequencing was performed to determine differentially expressed gene-enriched pathways following heparin lyase III treatment. Pathway analysis demonstrated downregulation of genes that support cell junction integrity, EC polarity, and EC senescence while upregulating genes that promote cell differentiation and proliferation following HS shedding.
Published in
Trauma promotes heparan sulfate modifications and cleavage that disrupt homeostatic gene expression in microvascular endothelial cells
Richter RP, Odum JD, Margaroli C et al. · Frontiers in cell and developmental biology 2024 · PMID 39114570 · doi:10.3389/fcell.2024.1390794
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Also filed as BioProject PRJNA1082369 and SRA study SRP492687. Searching any of these in the dataset finder brings you back here.

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