Knockdown of lncRNA Gm11974 protect against cerebral ischemic reperfusion through miR-766-3p/NR3C2 axis

Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):3847-3853. doi: 10.1080/21691401.2019.1666859.

Abstract

Aims: In previous studies, numerous differential lncRNAs in cerebral ischemic reperfusion injury were identified using RNA-Seq analysis. However, little is known about whether and how lncRNAs involved in cerebral I/R injury. In this study, we investigated the function and explored the possible mechanism of lncRNA Gm11974 in cerebral I/R injury. Methods: Oxygen glucose deprivation model in N2a cells were utilized to mimic the cerebral I/R injury in vitro. Trypan blue staining, Tunel, JC-1 and cell viability were measured to evaluate the function of lncRNA Gm11974. Dual-luciferase reporter assay was used to explore the potential mechanism of lncRNA Gm11974. Results: Gm11974 was mainly located in cytoplasm. Knockdown of lncRNA Gm11974 alleviated the apoptosis induced by OGD and cell death rates were significantly reduced. We further provided the possible mechanism that Gm11974/miR-766-3p/NR3C2 axis plays important role in cerebral I/R injury. Conclusions: We evaluated the function and mechanism of lncRNA Gm11974 in ischemic brain injury. LncRNA Gm11974 may serve as a potential target for new therapeutic intervention.

Keywords: Apoptosis; Gm11974; ischemic stroke; miR-766-3p.

MeSH terms

  • Base Sequence
  • Brain Ischemia / complications*
  • Cell Hypoxia / genetics
  • Gene Knockdown Techniques*
  • Glucose / metabolism
  • HEK293 Cells
  • Humans
  • MicroRNAs / genetics*
  • Oxygen / metabolism
  • RNA, Long Noncoding / genetics*
  • RNA, Long Noncoding / metabolism
  • Receptors, Mineralocorticoid / metabolism*
  • Reperfusion Injury / genetics
  • Reperfusion Injury / metabolism
  • Reperfusion Injury / pathology
  • Reperfusion Injury / prevention & control*

Substances

  • MIRN766 microRNA, human
  • MicroRNAs
  • NR3C2 protein, human
  • RNA, Long Noncoding
  • Receptors, Mineralocorticoid
  • Glucose
  • Oxygen