Histone methyltransferase Smyd2 contributes to blood-brain barrier breakdown in stroke

Clin Transl Med. 2022 Mar;12(3):e761. doi: 10.1002/ctm2.761.

Abstract

Background: The blood-brain barrier (BBB) plays a principal role in the healthy and diseased central nervous systems, and BBB disruption after ischaemic stroke is responsible for increased mortality. Smyd2, a member of the SMYD-methyltransferase family, plays a vital role in disease by methylation of diverse substrates; however, little is known about its role in the pathophysiology of the brain in response to ischaemia-reperfusion injury.

Methods: Using oxygen glucose deprivation and reoxygenation (OGD/R)-induced primary brain microvascular endothelial cells (BMECs) and Smyd2 knockdown mice subjected to middle cerebral artery occlusion, we evaluated the role of Smyd2 in BBB disruption. We performed loss-of-function and gain-of-function studies to investigate the biological function of Smyd2 in ischaemic stroke.

Results: We found that Smyd2 was a critical factor for regulating brain endothelial barrier integrity in ischaemia-reperfusion injury. Smyd2 is upregulated in peri-ischaemic brains, leading to BBB disruption via methylation-mediated Sphk/S1PR. Knockdown of Smyd2 in mice reduces BBB permeability and improves functional recovery. Using OGD/R-induced BMECs, we demonstrated that Sphk/S1PR methylation modification by Smyd2 affects ubiquitin-dependent degradation and protein stability, which may disrupt endothelial integrity. Moreover, overexpression of Smyd2 can damage endothelial integrity through Sphk/S1PR signalling.

Conclusions: Overall, these results reveal a novel role for Smyd2 in BBB disruption in ischaemic stroke, suggesting that Smyd2 may represent a new therapeutic target for ischaemic stroke.

Keywords: Smyd2; blood-brain barrier; brain microvascular endothelial cells; ischaemia stroke.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood-Brain Barrier / metabolism
  • Brain Ischemia* / metabolism
  • Endothelial Cells / metabolism
  • Glucose / metabolism
  • Histone Methyltransferases / metabolism
  • Histone-Lysine N-Methyltransferase
  • Ischemic Stroke*
  • Mice
  • Oxygen / metabolism
  • Reperfusion Injury* / metabolism
  • Stroke* / genetics
  • Stroke* / metabolism

Substances

  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase
  • Smyd2 protein, mouse
  • Glucose
  • Oxygen