An antibody that targets cell-surface glucose-regulated protein-78 inhibits expression of inflammatory cytokines and plasminogen activator inhibitors by macrophages

J Cell Biochem. 2023 May;124(5):743-752. doi: 10.1002/jcb.30401. Epub 2023 Mar 22.

Abstract

Glucose-regulated protein-78 (Grp78) is an endoplasmic reticulum chaperone, which is secreted by cells and associates with cell surfaces, where it functions as a receptor for activated α2 -macroglobulin (α2 M) and tissue-type plasminogen activator (tPA). In macrophages, α2 M and tPA also bind to the transmembrane receptor, LDL receptor-related protein-1 (LRP1), activating a cell-signaling receptor assembly that includes the NMDA receptor (NMDA-R) to suppress innate immunity. Herein, we demonstrate that an antibody targeting Grp78 (N88) inhibits NFκB activation and expression of proinflammatory cytokines in bone marrow-derived macrophages (BMDMs) treated with the toll-like receptor-4 (TLR4) ligand, lipopolysaccharide, or with agonists that activate TLR2, TLR7, or TLR9. Pharmacologic inhibition of the NMDA-R or deletion of the gene encoding LRP1 (Lrp1) in BMDMs neutralizes the activity of N88. The fibrinolysis protease inhibitor, plasminogen activator inhibitor-1 (PAI1), has been implicated in diverse diseases including metabolic syndrome, cardiovascular disease, and type 2 diabetes. Deletion of Lrp1 independently increased expression of PAI1 and PAI2 in BMDMs, as did treatment of wild-type BMDMs with TLR agonists. tPA, α2 M, and N88 inhibited expression of PAI1 and PAI2 in BMDMs treated with TLR-activating agents. Inhibiting Src family kinases blocked the ability of both N88 and tPA to function as anti-inflammatory agents, suggesting that the cell-signaling pathway activated by tPA and N88, downstream of LRP1 and the NMDA-R, may be equivalent. We conclude that targeting cell-surface Grp78 may be effective in suppressing innate immunity by a mechanism that requires LRP1 and the NMDA-R.

Keywords: LRP1; NMDA receptor; PAI1; PAI2; glucose-regulated protein-78; tissue-type plasminogen activator; α2-macroglobulin.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antibodies
  • Cytokines* / metabolism
  • Diabetes Mellitus, Type 2* / metabolism
  • Endoplasmic Reticulum Chaperone BiP
  • Humans
  • Low Density Lipoprotein Receptor-Related Protein-1 / genetics
  • Low Density Lipoprotein Receptor-Related Protein-1 / metabolism
  • Macrophages / metabolism
  • Membrane Proteins / metabolism
  • N-Methylaspartate / metabolism
  • Plasminogen Inactivators / metabolism

Substances

  • Cytokines
  • Membrane Proteins
  • Plasminogen Inactivators
  • Endoplasmic Reticulum Chaperone BiP
  • N-Methylaspartate
  • Antibodies
  • Low Density Lipoprotein Receptor-Related Protein-1