Growth factors and components for extracellular proteolysis are differentially expressed during in vitro maturation of bovine cumulus-oocyte complexes

Biol Reprod. 1998 Oct;59(4):801-6. doi: 10.1095/biolreprod59.4.801.

Abstract

In the present study, the time-dependent collagenolytic potential and mRNA transcription of extracellular matrix (ECM)-degrading components, transforming growth factor beta1 (TGFbeta1), and both basic fibroblast growth factor (bFGF) and FGF receptors (FGFR) in bovine cumulus-oocyte complexes (COCs) were investigated during 24 h of in vitro maturation (IVM). COCs were collected from 2- to 6-mm follicles, cultured in maturation medium, and sequentially removed at 3-h intervals for analysis. From 285 oocytes matured under these conditions, 114 (40.0%) developed to blastocysts on Day 9 after fertilization. Gelatin zymograms revealed protease activity at about 55 kDa for COCs matured for at least 3 h and two additional proteolytic zones at about 70 kDa after at least 9 h of IVM. The mRNAs of ECM-degrading components urokinase-type plasminogen activator (uPA), plasminogen activator inhibitor 1 (PAI1), matrix metalloproteinase 1 (MMP1), and tissue inhibitor of metalloproteinases 1 (TIMP1), as well as TGFbeta1, bFGF, and FGFR, were detected during IVM in a factor-specific pattern: all transcript levels found at COC 0 generally increased after 3 h of maturation and either remained high or decreased thereafter. On the basis of the chosen reverse transcription-polymerase chain reaction technique, one could suggest relative higher mRNA concentrations for TIMP1, PAI1, and both growth factors compared to uPA, MMP1, and FGFR. Our results suggest a finely tuned extracellular proteolysis during IVM of bovine COCs, for which the concerted action of modulating growth factors like bFGF and TGFbeta1 may be essential.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Female
  • Growth Substances / biosynthesis*
  • Growth Substances / genetics
  • In Vitro Techniques
  • Oocytes / enzymology
  • Oocytes / growth & development*
  • Oocytes / metabolism*
  • Peptide Hydrolases / biosynthesis*
  • Peptide Hydrolases / genetics
  • RNA, Messenger / biosynthesis
  • Receptors, Growth Factor / biosynthesis
  • Receptors, Growth Factor / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription, Genetic

Substances

  • Growth Substances
  • RNA, Messenger
  • Receptors, Growth Factor
  • Peptide Hydrolases