Cyclic expression of mRNA transcripts for connective tissue components in the mouse ovary

Mol Hum Reprod. 1999 Sep;5(9):803-8. doi: 10.1093/molehr/5.9.803.

Abstract

In the ovary, differentiation of germinal cells into primordial follicles, functional ovulatory follicles and corpus luteum, all take place in a connective tissue matrix. We postulated that extracellular matrix (ECM) of the ovary participates actively in ovarian functions. To test this, the mRNA levels for several ECM components were determined in the mouse ovary at six distinct stages of the 4-day oestrous cycle. Northern analysis revealed statistically significant cyclic expression patterns for the mRNAs coding for type III, IV and VI collagens as well as for the small proteoglycan, biglycan, and for syndecan-1 and osteonectin. The cyclic changes observed in the mRNAs for these structural components exceeded those for matrix metalloproteinases (MMP)-2, -9 and -13, and for tissue inhibitors of matrix metalloproteinases (TIMP)-1, -2 and -3, where the changes were not statistically significant, despite their apparent role in ECM remodelling in the ovary. These observations support the hypothesis that cyclic changes in the production and degradation of ECM are part of normal ovarian function connected with follicular maturation, rupture and corpus luteum formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biglycan
  • Blotting, Northern
  • Carrier Proteins / genetics
  • Collagen / genetics*
  • Connective Tissue / chemistry
  • Connective Tissue / physiology
  • Connective Tissue Cells / physiology
  • Decorin
  • Estrus / physiology
  • Extracellular Matrix Proteins / genetics
  • Female
  • Fibromodulin
  • Gene Expression Regulation
  • Matrix Metalloproteinase 2 / genetics*
  • Matrix Metalloproteinase 9 / genetics
  • Membrane Glycoproteins / genetics
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Osteonectin / genetics
  • Ovary / cytology*
  • Ovary / physiology*
  • Proteoglycans / genetics*
  • RNA, Messenger / analysis*
  • Syndecan-1
  • Syndecans
  • Tissue Inhibitor of Metalloproteinase-1 / genetics
  • Tissue Inhibitor of Metalloproteinase-2 / genetics
  • Tissue Inhibitor of Metalloproteinase-3 / genetics
  • Transcription, Genetic

Substances

  • Bgn protein, mouse
  • Biglycan
  • Carrier Proteins
  • Dcn protein, mouse
  • Decorin
  • Extracellular Matrix Proteins
  • Fmod protein, mouse
  • Membrane Glycoproteins
  • Osteonectin
  • Proteoglycans
  • RNA, Messenger
  • Sdc1 protein, mouse
  • Syndecan-1
  • Syndecans
  • Tissue Inhibitor of Metalloproteinase-1
  • Tissue Inhibitor of Metalloproteinase-3
  • Fibromodulin
  • Tissue Inhibitor of Metalloproteinase-2
  • Collagen
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9