Functional significance of MMP-9 in tumor necrosis factor-induced proliferation and branching morphogenesis of mammary epithelial cells

Endocrinology. 2000 Oct;141(10):3764-73. doi: 10.1210/endo.141.10.7697.


Tissue remodeling is a key process involved in normal mammary gland development, with matrix metalloproteinases (MMPs) playing an important role in this process. Our laboratory has demonstrated that tumor necrosis factor (TNF) stimulates branching morphogenesis of mammary epithelial cells (MEC) within a reconstituted basement membrane. Studies were therefore undertaken to determine whether MMPs might mediate the effects of TNF. Using a primary culture model in which rat MEC grow three-dimensionally within a reconstituted basement membrane, we found that TNF stimulated secretion of MMP-9 but not MMP-2. To determine whether MMP-9 was involved in TNF-induced proliferation and branching morphogenesis, we used a peptide containing the prodomain sequence of MMPs and two MMP inhibitors. Both the prodomain peptide (5 x 10(-4)-10(-3) M), as well as BB-94 (10(-8)-10(-5) M) and CGS 27023A (10(-6)-10(-5) M), inhibited TNF-induced proliferation and branching morphogenesis in a concentration-dependent manner. Finally, to verify the specific requirement for MMP-9, we demonstrated that an MMP-9 neutralizing antibody blocked TNF-induced proliferation and branching morphogenesis. Together, these data suggest that TNF-regulated MMP-9 may play a role in the controlled invasion of the fad pad that occurs during normal mammary gland development and that misregulation of MMP-9 may contribute to the invasiveness of breast cancer.

Publication types

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

MeSH terms

  • Animals
  • Antibodies / pharmacology
  • Cell Division / physiology
  • Cells, Cultured
  • Enzyme Induction
  • Epithelial Cells / cytology
  • Female
  • Hydroxamic Acids*
  • Mammary Glands, Animal / cytology*
  • Matrix Metalloproteinase 9 / immunology
  • Matrix Metalloproteinase 9 / metabolism
  • Matrix Metalloproteinase 9 / physiology*
  • Phenylalanine / analogs & derivatives*
  • Phenylalanine / pharmacology
  • Protease Inhibitors / pharmacology
  • Pyrazines*
  • Rats
  • Rats, Sprague-Dawley
  • Sulfonamides
  • Thiophenes / pharmacology
  • Tumor Necrosis Factor-alpha / pharmacology
  • Tumor Necrosis Factor-alpha / physiology*


  • Antibodies
  • CGS 27023A
  • Hydroxamic Acids
  • Protease Inhibitors
  • Pyrazines
  • Sulfonamides
  • Thiophenes
  • Tumor Necrosis Factor-alpha
  • Phenylalanine
  • batimastat
  • Matrix Metalloproteinase 9