Matrilysin (matrix metalloproteinase-7) mediates E-cadherin ectodomain shedding in injured lung epithelium

Am J Pathol. 2003 Jun;162(6):1831-43. doi: 10.1016/S0002-9440(10)64318-0.


Matrilysin (matrix metalloproteinase-7) is highly expressed in lungs of patients with pulmonary fibrosis and other conditions associated with airway and alveolar injury. Although matrilysin is required for closure of epithelial wounds ex vivo, the mechanism of its action in repair is unknown. We demonstrate that matrilysin mediates shedding of E-cadherin ectodomain from injured lung epithelium both in vitro and in vivo. In alveolar-like epithelial cells, transfection of activated matrilysin resulted in shedding of E-cadherin and accelerated cell migration. In vivo, matrilysin co-localized with E-cadherin at the basolateral surfaces of migrating tracheal epithelium, and the reorganization of cell-cell junctions seen in wild-type injured tissue was absent in matrilysin-null samples. E-cadherin ectodomain was shed into the bronchoalveolar lavage fluid of bleomycin-injured wild-type mice, but was not shed in matrilysin-null mice. These findings identify E-cadherin as a novel substrate for matrilysin and indicate that shedding of E-cadherin ectodomain is required for epithelial repair.

Publication types

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

MeSH terms

  • Animals
  • Binding Sites
  • Bleomycin / administration & dosage
  • Cadherins / metabolism*
  • Cell Communication
  • Cell Line
  • Cell Movement / physiology
  • Culture Techniques
  • Epithelial Cells / metabolism*
  • Epithelial Cells / pathology
  • Fibrosis
  • HT29 Cells
  • Humans
  • Lung / drug effects
  • Lung / metabolism
  • Lung / pathology
  • Matrix Metalloproteinase 7 / genetics
  • Matrix Metalloproteinase 7 / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microscopy, Confocal
  • Microscopy, Electron
  • Protein Binding
  • Pulmonary Alveoli / metabolism
  • Pulmonary Alveoli / pathology
  • Trachea / cytology
  • Trachea / metabolism
  • Trachea / ultrastructure
  • Transfection
  • Tumor Cells, Cultured


  • Cadherins
  • Bleomycin
  • Matrix Metalloproteinase 7