bioRxiv · 10.1101/2021.08.30.458308
miR-573 rescues endothelial dysfunction during dengue infection under PPARγ regulation.
Abstract
Early prognosis of abnormal vasculopathy is essential for effective clinical management of severe dengue patients. An exaggerated interferon (IFN) response and release of vasoactive factors from endothelial cells cause vasculopathy. This study shows that dengue 2 (DENV2) infection of human umbilical vein endothelial cells (HUVEC) results in differentially regulated miRNAs important for endothelial function. miR-573 was significantly down-regulated in DENV2-infected HUVEC due to decreased Peroxisome Proliferator Activator Receptor Gamma (PPAR{gamma}) activity. Restoring miR-573 expression decreased endothelial permeability by suppressing the expression of vasoactive angiopoietin 2 (ANGPT2). We also found that miR-573 suppressed the proinflammatory IFN response through direct downregulation of toll like receptor 2 (TLR2) expression. Our study provides a novel insight into miR-573 mediated regulation of endothelial function during DENV2 infection which can be further translated into a potential therapeutic and prognostic agent for severe dengue patients.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Banerjee, S., Wein Xin, C., Chu, J. J. H.. 2021-09-01. miR-573 rescues endothelial dysfunction during dengue infection under PPARγ regulation.. https://doi.org/10.1101/2021.08.30.458308
Cite the original work for its findings. Save a collection to share your selection of sources.