Long Non-coding RNA PVT1 Inhibits miR-30c-5p to Upregulate Rock2 to Modulate Cerebral Ischemia/Reperfusion Injury Through MAPK Signaling Pathway Activation

Mol Neurobiol. 2021 Nov;58(11):6032-6048. doi: 10.1007/s12035-021-02539-y. Epub 2021 Aug 26.

Abstract

Long non-coding RNAs (lncRNAs) play a key role in a variety of disease processes. Plasmacytoma variant translocation 1 (PVT1), a lncRNA, is known to regulate cell functions and play a key role in the pathogenesis of many malignant tumors. The function and molecular mechanisms of lncRNA-PVT1 in cerebral ischemia remain unknown. Real-time PCR (qRT-PCR) was used to detect lncRNA-PVT1 and microRNA-30c-5p (miR-30c-5p) expression in the brain tissues of mice underwent middle cerebral artery occlusion/reperfusion (MCAO/R) and oxygen-glucose deprivation/reperfusion (OGD/R)-treated mouse primary brain neurons. Gain- or loss-of-function approaches were used to manipulate PVT1, miR-30c-5p, and Rho-associated protein kinase 2 (Rock2). The mechanism of PVT1 in ischemic stroke was evaluated both in vivo and in vitro via bioinformatics analysis, CCK-8, flow cytometry, TUNEL staining, luciferase activity assay, RNA FISH, and Western blot. PVT1 was upregulated in the brain tissues of mice treated with MCAO/R and primary cerebral cortex neurons of mice treated with OGD/R. Mechanistically, PVT1 knockdown resulted in a lower infarct volume and ameliorated neurobehavior in MCAO mice. Consistent with in vivo results, PVT1 upregulation significantly decreased the viability and induced apoptosis of neurons cultured in OGD/R. Moreover, we demonstrated that PVT1 acts as a competitive endogenous RNA (ceRNA) that competes with miR-30c-5p, thereby negatively regulating its endogenous target Rock2. Overexpression of miR-30c-5p significantly promoted cell proliferation and inhibited apoptosis. Meanwhile, PVT1 was confirmed to target miR-30c-5p, thus activating Rock2 expression, which finally led to the activation of MAPK signaling. We demonstrated that PVT1, as a ceRNA of miR-30c-5p, could target and regulate the level of Rock2, which aggravates cerebral I/R injury via activation of the MAPK pathway. These findings reveal a new function of PVT1, which helps to broadly understand cerebral ischemic stroke and provide a new treatment strategy for this disease.

Keywords: Cerebral ischemia; MAPK signaling; Rock2; lncRNA-PVT1; miR-30c-5p.

MeSH terms

  • Animals
  • Apoptosis
  • Cell Division
  • Cell Hypoxia
  • Cells, Cultured
  • Epigenesis, Genetic
  • Gain of Function Mutation
  • Gene Knockdown Techniques
  • Glucose / pharmacology
  • Infarction, Middle Cerebral Artery / genetics
  • Infarction, Middle Cerebral Artery / metabolism*
  • Loss of Function Mutation
  • MAP Kinase Signaling System / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / antagonists & inhibitors
  • MicroRNAs / genetics
  • Neurons / drug effects
  • Neurons / metabolism
  • Oxygen / pharmacology
  • RNA Interference
  • RNA, Long Noncoding / genetics
  • RNA, Long Noncoding / physiology*
  • RNA, Small Interfering / genetics
  • Reperfusion Injury / genetics
  • Reperfusion Injury / metabolism*
  • Subcellular Fractions / chemistry
  • Up-Regulation
  • rho-Associated Kinases / biosynthesis*
  • rho-Associated Kinases / genetics

Substances

  • MIRN30c-1 microRNA, mouse
  • MicroRNAs
  • PVT1 long-non-coding RNA, mouse
  • RNA, Long Noncoding
  • RNA, Small Interfering
  • Rock2 protein, mouse
  • rho-Associated Kinases
  • Glucose
  • Oxygen