Enhanced Expression of PD-L1 on Microglia After Surgical Brain Injury Exerts Self-Protection from Inflammation and Promotes Neurological Repair

Neurochem Res. 2019 Nov;44(11):2470-2481. doi: 10.1007/s11064-019-02864-8. Epub 2019 Sep 3.

Abstract

Neuroinflammation and brain edema are major complications in the pathophysiology of surgical brain injury (SBI). Programmed death-ligand 1 (PD-L1), an immune inhibitory receptor ligand, has been increasingly investigated for inhibition of T cell-mediated immunity and braking inflammatory response. However, the negative immunomodulatory capacity of PD-L1 and their possible mechanism in SBI is not yet clear. This study aimed to evaluate the expression and the role of PD-L1 in a mouse model of SBI induced inflammation and to further study the potential therapeutic effects of PD-L1 on SBI. Here we showed that PD-L1 expression was markedly elevated in the surrounding peri-resection brain tissue post-SBI in vivo. PD-L1 was up-regulated through ERK signal pathway in LPS-treated BV-2 cells in vitro. Furthermore, blockade of the PD-L1 checkpoint using PD-L1 antibody significantly enhanced brain edema, exacerbated apoptosis and increased neurodeficits post-SBI. Moreover, activated PD-1/PD-L1 with PD-L1 protein significantly attenuated the inflammation responses and brain edema post-SBI. These results suggest that enhanced expression of PD-L1 post-SBI exerts self-protection from inflammation and promotes neurological repair. PD-L1 signal may have therapeutic potential for neurodegenerative disorders.

Keywords: Astrocyte; Microglia; Programmed death 1; Programmed death ligand 1; Surgical brain injury.

MeSH terms

  • Animals
  • Astrocytes / metabolism
  • B7-H1 Antigen / metabolism*
  • Brain / metabolism*
  • Brain / pathology
  • Brain / surgery
  • Brain Edema / metabolism
  • Brain Injuries / metabolism*
  • Cell Line
  • Female
  • Inflammation / metabolism*
  • Lipopolysaccharides / pharmacology
  • MAP Kinase Signaling System / drug effects
  • Mice, Inbred C57BL
  • Microglia / metabolism
  • Up-Regulation / drug effects

Substances

  • B7-H1 Antigen
  • Cd274 protein, mouse
  • Lipopolysaccharides