TSG-6 interacts with hyaluronan and aggrecan in a pH-dependent manner via a common functional element: implications for its regulation in inflamed cartilage

FEBS Lett. 1998 May 29;428(3):171-6. doi: 10.1016/s0014-5793(98)00523-7.

Abstract

Cartilage matrix is stabilised by the interactions of proteins with hyaluronan (HA). We compare the pH dependences of HA binding by aggrecan, link protein and TSG-6. Aggrecan and link protein exhibit maximal binding across a wide pH range (6.0-8.0). TSG-6, a protein that is only produced during inflammation, binds maximally at about pH 6.0 but shows a dramatic loss of function with increasing pH. TSG-6 also interacts with aggrecan, with a similar pH dependence, and this can be inhibited by HA. Thus, a common binding surface on TSG-6 may be involved in HA and aggrecan binding. We propose that TSG-6 is involved in matrix dissociation and that this is regulated by pH gradients in cartilage.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aggrecans
  • Binding Sites
  • Cartilage / physiology
  • Cartilage / physiopathology
  • Cell Adhesion Molecules / chemistry*
  • Cell Adhesion Molecules / metabolism*
  • Chondroitin Sulfate Proteoglycans / metabolism
  • Extracellular Matrix Proteins*
  • Humans
  • Hyaluronic Acid / metabolism*
  • Hydrogen-Ion Concentration*
  • Inflammation
  • Kinetics
  • Lectins, C-Type
  • Nuclear Magnetic Resonance, Biomolecular
  • Protein Conformation
  • Proteoglycans / metabolism*

Substances

  • Aggrecans
  • Cell Adhesion Molecules
  • Chondroitin Sulfate Proteoglycans
  • Extracellular Matrix Proteins
  • Lectins, C-Type
  • Proteoglycans
  • TNFAIP6 protein, human
  • Hyaluronic Acid