TSG-6 (Tumor Necrosis Factor-α-Stimulated Gene/Protein-6): An Emerging Remedy for Renal Inflammation

Hypertension. 2023 Jan;80(1):35-42. doi: 10.1161/HYPERTENSIONAHA.122.19431. Epub 2022 Nov 11.

Abstract

The inflammatory response is a major pathological feature in most kidney diseases and often evokes compensatory mechanisms. Recent evidence suggests that TSG-6 (tumor necrosis factor-α-stimulated gene/protein-6) plays a pivotal role in anti-inflammation in various renal diseases, including immune-mediated and nonimmune-mediated renal diseases. TSG-6 has a diverse repertoire of anti-inflammatory functions: it potentiates antiplasmin activity of IαI (inter-α-inhibitor) by binding to its light chain, crosslinks hyaluronan to promote its binding to cell surface receptor CD44, and thereby regulate the migration and adhesion of lymphocytes, inhibits chemokine-stimulated transendothelial migration of neutrophils by directly interacting with the glycosaminoglycan binding site of CXCL8 (CXC motif chemokine ligand-8), and upregulates COX-2 (cyclooxygenase-2) to produce anti-inflammatory metabolites. Hopefully, further developments can target this anti-inflammatory molecule to the kidney and harness its remedial properties. This review provides an overview of the emerging role of TSG-6 in blunting renal inflammation.

Keywords: TSG-6; cytokines; hyaluronan; renal inflammation.

Publication types

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

MeSH terms

  • Cell Adhesion Molecules* / genetics
  • Cyclooxygenase 2
  • Humans
  • Inflammation
  • Kidney Diseases*

Substances

  • TNFAIP6 protein, human
  • Cell Adhesion Molecules
  • CD44 protein, human
  • CXCL8 protein, human
  • Cyclooxygenase 2