1. Academic Validation
  2. Celastrol assuages oxygen-glucose deprivation and reoxygenation-induced damage in human brain microvascular endothelial cells through the circDLGAP4/miR-6085/GDF11 pathway

Celastrol assuages oxygen-glucose deprivation and reoxygenation-induced damage in human brain microvascular endothelial cells through the circDLGAP4/miR-6085/GDF11 pathway

  • Metab Brain Dis. 2022 Nov 29. doi: 10.1007/s11011-022-01106-1.
Chunhong Liu 1 Jiahui Gu 2 Yingli Yu 3
Affiliations

Affiliations

  • 1 Department of Traditional Chinese Medicine, Yantai Hospital of Traditional Chinese Medicine, No.39 Xing Fu road in Zhifu District, Yantai, 264013, China.
  • 2 Department of Pharmacy, Yantai Hospital of Traditional Chinese Medicine, Yantai, China.
  • 3 Department of Traditional Chinese Medicine, Yantai Hospital of Traditional Chinese Medicine, No.39 Xing Fu road in Zhifu District, Yantai, 264013, China. yyl19781026yt@163.com.
Abstract

The effect of Celastrol on cerebral ischemia-reperfusion remains unknown. The study aims to explore the role of circular RNA DLGAP4 (circDLGAP4) in cerebral ischemia-reperfusion and the underlying mechanism. Ischemia-reperfusion (I/R) injury of human brain microvascular endothelial cells (HBMECs) was induced by oxygen-glucose deprivation and reoxygenation (OGD/R). Reverse transcription quantitative Real-Time PCR (RT-qPCR) and western blotting analysis were performed to detect the expression of circDLGAP4, microRNA-6085 (miR-6085), Growth Differentiation Factor 11 (GDF11), B-cell lymphoma-2 (BCL2) and BCL2-associated x protein (Bax). Cell viability, proliferation, and Apoptosis were analyzed by cell counting kit-8, 5-Ethynyl-2'-deoxyuridine and flow cytometry analysis. Oxidative stress was analyzed by evaluating the levels of Malondialdehyde (MDA) and Reactive Oxygen Species (ROS) and the activity of Superoxide Dismutase (SOD). The associations among circDLGAP4, miR-6085 and GDF11 were identified by dual-luciferase reporter, RNA immunoprecipitation (RIP) and RNA pull-down assays. Celastrol reduced OGD/R-induced inhibition of circDLGAP4 expression in HBMECs. Celastrol treatment protected HBMECs from OGD/R-induced cell proliferation inhibition and Apoptosis and oxidative stress promotion; however, circDLGAP4 depletion attenuated these effects. CircDLGAP4 acted as a Sponge for miR-6085, and miR-6085 mimics restored circDLGAP4-mediated effects in OGD/R-stimulated HBMECs. In addition, GDF11 was identified as a targte of miR-6085, and participated in the regulation of miR-6085 to OGD/R-induced HBMEC damage. Further, circDLGAP4 absence inhibited GDF11 expression by interacting with miR-6085 under Celastrol treatment. Celastrol ameliorated OGD/R-induced HBMEC Apoptosis and oxidative stress by circDLGAP4/miR-6085/GDF11 pathway, supporting the use of Celastrol as a therapeutic agent for cerebral infarction.

Keywords

Celastrol; GDF11; cerebral infarction; circDLGAP4; miR-6085.

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