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Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Circular RNA hsa_circ_0003575 regulates oxLDL induced vascular endothelial cells proliferation and angiogenesis
Chen-Ye Li1, Lan Ma1, Bo Yu2
1Department of Geratology, 2nd Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Abstract:
Circular RNAs (circRNAs) are a novel class of RNAs generated from back-splicing and characterized by covalently closed continuous loops. Recently, circRNAs have recently shown large regulation on cardiovascular system, including atherosclerosis. The present study aims to investigate the circRNA expression profile and identify their roles on vascular endothelial cells induced by oxLDL. Human circRNA microarray analysis revealed that total 943 differently expressed circRNAs were screened with 2 fold change. Hsa_circ_0003575 was validated to be significantly up-regulated in oxLDL induced HUVECs. Loss-of-function experiments indicated that hsa_circ_0003575 silencing promoted the proliferation and angiogenesis ability of HUVECs. Bioinformatics online programs predicted the potential circRNA-miRNA-mRNA network for hsa_circ_0003575. In summary, circRNA microarray analysis reveals the expression profiles of HUVECs and verifies the role of hsa_circ_0003575 on HUVECs, providing a therapeutic strategy for vascular endothelial cell injury of atherosclerosis.
Insights
Circular RNAs (circRNAs) regulate cardiovascular health, including atherosclerosis. This study identifies hsa_circ_0003575 as upregulated in oxLDL-induced endothelial cells, promoting proliferation and angiogenesis.
Area of Science:
- Molecular Biology
- Cardiovascular Research
- Genomics
Background:
- Circular RNAs (circRNAs) are covalently closed RNA molecules with emerging roles in cellular regulation.
- Dysregulation of circRNAs is implicated in cardiovascular diseases like atherosclerosis.
- Oxidized low-density lipoprotein (oxLDL) is a key factor in endothelial cell dysfunction during atherosclerosis.
Purpose of the Study:
- To investigate the circRNA expression profile in oxLDL-induced human umbilical vein endothelial cells (HUVECs).
- To identify specific circRNAs involved in endothelial cell responses to oxLDL.
- To elucidate the functional role of identified circRNAs in atherosclerosis pathogenesis.
Main Methods:
- Human circRNA microarray analysis to screen differentially expressed circRNAs.
- Validation of specific circRNAs using quantitative methods.
- Loss-of-function experiments to assess the impact of circRNA silencing on HUVEC function.
- Bioinformatic analysis to predict circRNA-miRNA-mRNA interactions.
Main Results:
- Microarray analysis identified 943 differentially expressed circRNAs (2-fold change) in oxLDL-treated HUVECs.
- Hsa_circ_0003575 was significantly upregulated in oxLDL-induced HUVECs.
- Silencing of hsa_circ_0003575 enhanced HUVEC proliferation and angiogenesis.
- Predicted circRNA-miRNA-mRNA networks provide insights into hsa_circ_0003575 regulatory mechanisms.
Conclusions:
- CircRNA expression profiling reveals significant alterations in HUVECs exposed to oxLDL.
- Hsa_circ_0003575 plays a crucial role in promoting HUVEC proliferation and angiogenesis.
- Hsa_circ_0003575 represents a potential therapeutic target for vascular endothelial cell injury in atherosclerosis.
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