Circular RNA circCCDC9 alleviates ischaemic stroke ischaemia/reperfusion injury via the Notch pathway

J Cell Mol Med. 2020 Dec;24(24):14152-14159. doi: 10.1111/jcmm.16025. Epub 2020 Oct 29.

Abstract

Stroke is a leading cause of death and disability, while its pathophysiological mechanisms are not fully understood. In this study, we used the tMCAO mice model to investigate the role of circCCDC9 in the pathogenesis of stroke. We found that the expression of circCCDC9 was significantly decreased in the brains of tMCAO mice. The Evens blue and brain water content were significantly higher in the Pre-IR and Pre-IR+Vector mice, while these patterns were partially reversed by overexpression of circCCDC9. The nitrite content and eNOS expression were decreased in the Pre-IR and Pre-IR+Vector groups, which was restored by circCCDC9 overexpression. Overexpression of circCCDC9 also inhibited the expression of Caspase-3, Bax/Bcl-2 ratio and the expression of Notch1, NICD and Hes1 in tMCAO mice. Knockdown of circCCDC9 increased the expression of Caspase-3, Bax/Bcl-2 ratio and the expression of Notch1, NICD and Hes1. In summary, overexpression of circCCDC9 protected the blood-brain barrier and inhibited apoptosis by suppressing the Notch1 signalling pathway, while knockdown of circCCDC9 had the opposite effects. Our findings showed that circCCDC9 is a potential novel therapeutic target for cerebrovascular protection in acute ischaemic stroke.

Keywords: Notch pathway; cerebral ischaemia/reperfusion; circCCDC9.

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Blood-Brain Barrier / metabolism
  • Disease Models, Animal
  • Gene Expression Regulation
  • Gene Knockdown Techniques
  • Ischemic Stroke / etiology*
  • Ischemic Stroke / metabolism*
  • Ischemic Stroke / pathology
  • Male
  • Mice
  • Microtubule Proteins / genetics*
  • RNA, Circular*
  • Receptors, Notch / metabolism*
  • Reperfusion Injury / etiology*
  • Reperfusion Injury / metabolism*
  • Reperfusion Injury / pathology
  • Signal Transduction
  • Transcription Factor HES-1 / genetics
  • Transcription Factor HES-1 / metabolism

Substances

  • CCDC9 protein, human
  • Hes1 protein, mouse
  • Microtubule Proteins
  • RNA, Circular
  • Receptors, Notch
  • Transcription Factor HES-1