miR-1233-3p Inhibits Angiopoietin-1-Induced Endothelial Cell Survival, Migration, and Differentiation

Angiopoietin-1 (Ang-1) and its receptor Tie-2 promote vascular integrity and angiogenesis. MicroRNAs (miRNAs) are involved in the regulation of many cellular functions, including endothelial cell (EC) survival, proliferation, and differentiation. Several reports indicate that these effects of miRNAs...

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Main Authors: Veronica Sanchez, Sharon Harel, Anas Khalid Sa’ub, Dominique Mayaki, Sabah N. A. Hussain
Format: Article
Language:English
Published: MDPI AG 2025-01-01
Series:Cells
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Online Access:https://www.mdpi.com/2073-4409/14/2/75
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author Veronica Sanchez
Sharon Harel
Anas Khalid Sa’ub
Dominique Mayaki
Sabah N. A. Hussain
author_facet Veronica Sanchez
Sharon Harel
Anas Khalid Sa’ub
Dominique Mayaki
Sabah N. A. Hussain
author_sort Veronica Sanchez
collection DOAJ
description Angiopoietin-1 (Ang-1) and its receptor Tie-2 promote vascular integrity and angiogenesis. MicroRNAs (miRNAs) are involved in the regulation of many cellular functions, including endothelial cell (EC) survival, proliferation, and differentiation. Several reports indicate that these effects of miRNAs on EC functions are mediated through the modulation of angiogenesis factor signaling including that of vascular endothelial growth factor (VEGF). To date, very little is known about the roles played by miRNAs in the signaling and angiogenesis promoted by the Ang-1–Tie-2 receptor axis. Our high-throughput screening of miRNAs regulated by Ang-1 exposure in human umbilical vein endothelial cells (HUVECs) has identified miR-1233-3p as a mature miRNA whose cellular levels are significantly downregulated in response to Ang-1 exposure. The expression of miR-1233-3p in these cells is also downregulated by other angiogenesis factors including VEGF, fibroblast growth factor 2 (FGF-2), transforming growth factor β (TGFβ), and angiopoietin-2 (Ang-2). The overexpression of miR-1233-3p in HUVECs using specific mimics significantly attenuated cell survival, migration, and capillary-like tube formation, and promoted apoptosis. Moreover, miR-1233-3p overexpression resulted in reversal of the anti-apoptotic, pro-migration, and pro-differentiation effects of Ang-1. Biotinylated miRNA pull-down assays showed that p53 and DNA damage-regulated 1 (PDRG1) is a direct target of miR-1233-3p in HUVECs. The exposure of HUVECs to Ang-1, angiopoietin-2 (Ang-2), fibroblast growth factor 2 (FGF2), vascular endothelial growth factor (VEGF), or transforming growth factor β (TGFβ) triggers the regulation of PDRG1 expression. This study highlights that miR-1233-3p exerts inhibitory effects on Ang-1-induced survival, migration, and the differentiation of cultured ECs.
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spelling doaj-art-1fa93f3cb3bb4654bcd2395d3d8800a92025-01-24T13:26:35ZengMDPI AGCells2073-44092025-01-011427510.3390/cells14020075miR-1233-3p Inhibits Angiopoietin-1-Induced Endothelial Cell Survival, Migration, and DifferentiationVeronica Sanchez0Sharon Harel1Anas Khalid Sa’ub2Dominique Mayaki3Sabah N. A. Hussain4Meakins-Christie Laboratories, Department of Medicine, McGill University, Montreal, QC H4A 3J1, CanadaMeakins-Christie Laboratories, Department of Medicine, McGill University, Montreal, QC H4A 3J1, CanadaMeakins-Christie Laboratories, Department of Medicine, McGill University, Montreal, QC H4A 3J1, CanadaMeakins-Christie Laboratories, Department of Medicine, McGill University, Montreal, QC H4A 3J1, CanadaMeakins-Christie Laboratories, Department of Medicine, McGill University, Montreal, QC H4A 3J1, CanadaAngiopoietin-1 (Ang-1) and its receptor Tie-2 promote vascular integrity and angiogenesis. MicroRNAs (miRNAs) are involved in the regulation of many cellular functions, including endothelial cell (EC) survival, proliferation, and differentiation. Several reports indicate that these effects of miRNAs on EC functions are mediated through the modulation of angiogenesis factor signaling including that of vascular endothelial growth factor (VEGF). To date, very little is known about the roles played by miRNAs in the signaling and angiogenesis promoted by the Ang-1–Tie-2 receptor axis. Our high-throughput screening of miRNAs regulated by Ang-1 exposure in human umbilical vein endothelial cells (HUVECs) has identified miR-1233-3p as a mature miRNA whose cellular levels are significantly downregulated in response to Ang-1 exposure. The expression of miR-1233-3p in these cells is also downregulated by other angiogenesis factors including VEGF, fibroblast growth factor 2 (FGF-2), transforming growth factor β (TGFβ), and angiopoietin-2 (Ang-2). The overexpression of miR-1233-3p in HUVECs using specific mimics significantly attenuated cell survival, migration, and capillary-like tube formation, and promoted apoptosis. Moreover, miR-1233-3p overexpression resulted in reversal of the anti-apoptotic, pro-migration, and pro-differentiation effects of Ang-1. Biotinylated miRNA pull-down assays showed that p53 and DNA damage-regulated 1 (PDRG1) is a direct target of miR-1233-3p in HUVECs. The exposure of HUVECs to Ang-1, angiopoietin-2 (Ang-2), fibroblast growth factor 2 (FGF2), vascular endothelial growth factor (VEGF), or transforming growth factor β (TGFβ) triggers the regulation of PDRG1 expression. This study highlights that miR-1233-3p exerts inhibitory effects on Ang-1-induced survival, migration, and the differentiation of cultured ECs.https://www.mdpi.com/2073-4409/14/2/75angiogenesisendothelial cellsangiopoietinstie-2 receptorssignalingmicroRNAs
spellingShingle Veronica Sanchez
Sharon Harel
Anas Khalid Sa’ub
Dominique Mayaki
Sabah N. A. Hussain
miR-1233-3p Inhibits Angiopoietin-1-Induced Endothelial Cell Survival, Migration, and Differentiation
Cells
angiogenesis
endothelial cells
angiopoietins
tie-2 receptors
signaling
microRNAs
title miR-1233-3p Inhibits Angiopoietin-1-Induced Endothelial Cell Survival, Migration, and Differentiation
title_full miR-1233-3p Inhibits Angiopoietin-1-Induced Endothelial Cell Survival, Migration, and Differentiation
title_fullStr miR-1233-3p Inhibits Angiopoietin-1-Induced Endothelial Cell Survival, Migration, and Differentiation
title_full_unstemmed miR-1233-3p Inhibits Angiopoietin-1-Induced Endothelial Cell Survival, Migration, and Differentiation
title_short miR-1233-3p Inhibits Angiopoietin-1-Induced Endothelial Cell Survival, Migration, and Differentiation
title_sort mir 1233 3p inhibits angiopoietin 1 induced endothelial cell survival migration and differentiation
topic angiogenesis
endothelial cells
angiopoietins
tie-2 receptors
signaling
microRNAs
url https://www.mdpi.com/2073-4409/14/2/75
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AT sharonharel mir12333pinhibitsangiopoietin1inducedendothelialcellsurvivalmigrationanddifferentiation
AT anaskhalidsaub mir12333pinhibitsangiopoietin1inducedendothelialcellsurvivalmigrationanddifferentiation
AT dominiquemayaki mir12333pinhibitsangiopoietin1inducedendothelialcellsurvivalmigrationanddifferentiation
AT sabahnahussain mir12333pinhibitsangiopoietin1inducedendothelialcellsurvivalmigrationanddifferentiation