Two distinct populations of tumor necrosis factor-stimulated gene-6 protein in the extracellular matrix of expanded mouse cumulus cell-oocyte complexes

Arch Biochem Biophys. 2001 Oct 15;394(2):173-81. doi: 10.1006/abbi.2001.2552.

Abstract

After the luteinizing hormone surge, the cumulus cell-oocyte complexes (COCs) in the preovulatory follicles produce a viscoelastic extracellular matrix, a process that requires the synthesis of hyaluronan as well as the incorporation of some components of the inter-alpha-trypsin inhibitor (IalphaI) family. In this study we report, that a hyaluronan-binding protein, the translated product of tumor necrosis factor-stimulated gene-6 (TSG-6), is also specifically accumulated in this matrix. TSG-6 mRNA expression is quickly upregulated and peaks at approximately 1500 copies/cell 4 h after the ovulatory stimuli as assessed by quantitative reverse transcription-polymerase chain reaction. Immunohistochemistry reveals the colocalization of the TSG-6 protein and hyaluronan around the cumulus and granulosa cells. The TSG-6 protein exists in two distinct populations in the COC matrix as demonstrated by Western-blot analysis. One population is a monomer that is anchored to the matrix by a noncovalent interaction. The second population is a covalent complex with either of the heavy chains of IalphaI and is bound to hyaluronan through a strong interaction that is resistant to denaturing conditions. The specific incorporation of the TSG-6 protein into the COC matrix suggests a structural role for this molecule.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alpha-Globulins / chemistry
  • Alpha-Globulins / genetics
  • Alpha-Globulins / metabolism
  • Amino Acid Sequence
  • Animals
  • Blotting, Western
  • Cell Adhesion Molecules / chemistry
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism*
  • Cell Differentiation
  • Cells, Cultured
  • Extracellular Matrix / chemistry
  • Extracellular Matrix / metabolism*
  • Female
  • Follicular Phase
  • Hyaluronic Acid / metabolism
  • Immunohistochemistry
  • Macromolecular Substances
  • Mass Spectrometry
  • Mice
  • Molecular Sequence Data
  • Molecular Weight
  • Oocytes / cytology
  • Oocytes / drug effects
  • Oocytes / metabolism*
  • Ovarian Follicle / cytology
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Analysis, Protein
  • Up-Regulation

Substances

  • Alpha-Globulins
  • Cell Adhesion Molecules
  • Macromolecular Substances
  • RNA, Messenger
  • Tnfaip6 protein, mouse
  • inter-alpha-inhibitor
  • Hyaluronic Acid