Cross-linking by tissue transglutaminase-2 alters fibrinogen-directed macrophage proinflammatory activity

J Thromb Haemost. 2022 May;20(5):1182-1192. doi: 10.1111/jth.15670. Epub 2022 Feb 27.

Abstract

Background: The blood coagulation factor fibrin(ogen) can modulate inflammation by altering leukocyte activity. Analyses of fibrin(ogen)-mediated proinflammatory activity have largely focused on leukocyte integrin binding activity revealed by conversion of fibrinogen to a stabilized fibrin polymer by blood coagulation enzymes. In addition to coagulation enzymes, fibrinogen is a substrate for tissue transglutaminase-2 (TG2), a widely expressed enzyme that produces unique fibrinogen Aα-γ chain cross-linked products.

Objectives: We tested the hypothesis that TG2 dependent cross-linking alters the proinflammatory activity of surface-adhered fibrinogen.

Methods: Mouse bone marrow-derived macrophages (BMDMs) were cultured on tissue culture plates coated with fibrinogen or TG2-cross-linked fibrinogen (10 µg/ml) and then stimulated with lipopolysaccharide (LPS, 1 ng/ml) or vehicle for various times.

Results: In the absence of LPS stimulation, TG2-cross-linked fibrin(ogen) enhanced inflammatory gene induction (e.g., Tnfα) compared with unmodified fibrinogen. LPS stimulation induced mitogen-activated protein kinase phosphorylation, IκBα degradation, and expression of proinflammatory cytokines (e.g., tumor necrosis factor α) within 60 min. This initial cellular activation was unaffected by unmodified or TG2-cross-linked fibrinogen. In contrast, LPS induction of interleukin-10 mRNA and protein and STAT3 phosphorylation was selectively attenuated by TG2-cross-linked fibrinogen, which was associated with enhanced proinflammatory cytokine secretion by LPS-stimulated BMDMs at later time points (6 and 24 h).

Conclusions: The results indicate that atypical cross-linking by TG2 imparts unique proinflammatory activity to surface-adhered fibrinogen. The results suggest a novel coagulation-independent mechanism controlling fibrinogen-directed macrophage activation.

Keywords: fibrinogen; inflammation; lipopolysaccharide; macrophage; transglutaminase.

MeSH terms

  • Animals
  • Fibrin / metabolism
  • Fibrinogen / metabolism
  • Humans
  • Lipopolysaccharides*
  • Macrophages / metabolism
  • Mice
  • Protein Glutamine gamma Glutamyltransferase 2*
  • Transglutaminases / genetics
  • Transglutaminases / metabolism
  • Tumor Necrosis Factor-alpha

Substances

  • Lipopolysaccharides
  • TG2 protein, mouse
  • Tumor Necrosis Factor-alpha
  • Fibrin
  • Fibrinogen
  • Protein Glutamine gamma Glutamyltransferase 2
  • Transglutaminases