Relationship between expression of matrix metalloproteinases and migration of epidermal and in vitro generated Langerhans cells

Eur J Cell Biol. 2002 Jul;81(7):383-9. doi: 10.1078/0171-9335-00252.

Abstract

Langerhans cells (LC) are dendritic cells that capture foreign antigens and migrate with them to the regional lymph nodes where they are presented to naive T cells. The possible role of matrix metalloproteinase-9 (MMP-9) in migration was suggested following experiments in a mouse model and in human skin explants. Using in vitro generated LC (iLC) derived from CD34+ cord blood cells and epidermal LC (eLC), we investigated the correlation between MMP-9 and other MMPs production and cell migration. Cells were activated by Bandrowski's base (BB), a chemical allergen, or by recombinant birch pollen allergen 1 (rBetv 1). Contact with allergens triggered migration of these cells, with a maximum rate being reached after 24 h. Migration was preceded by production of MMP-2 and MMP-9; part of the molecules were recovered as pro-MMPs in cell culture supernatant and part were associated with cell membrane proteins. At the cellular level, membrane-type 1 (MT1) and MT3-MMP were also identified. Addition of tumor necrosis factor-alpha (TNF-alpha) initiated pro-MMP-2 and pro-MMP-9 production followed by cell migration in a dose-dependent manner. These data imply that TNF-alpha is a key molecule for MMP production and cell migration. Furthermore, activation of iLC with BB or rBet v 1 induced synthesis of TNF-a and expression of TNF RII on the cell membrane, suggesting an autocrine loop. In conclusion, membrane-associated MMP-2 and-9 rather than soluble MMPs appear to be involved in cell migration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allergens / pharmacology
  • Antigens, CD34 / metabolism
  • Antigens, Plant
  • Basement Membrane / metabolism
  • Cell Movement
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Epidermal Cells*
  • Epidermis / metabolism
  • Fetal Blood / cytology
  • Flow Cytometry
  • Gelatinases / metabolism
  • Humans
  • In Vitro Techniques
  • Kinetics
  • Langerhans Cells / cytology
  • Leukocytes, Mononuclear / metabolism
  • Matrix Metalloproteinase 2 / metabolism*
  • Matrix Metalloproteinase 9 / biosynthesis*
  • Matrix Metalloproteinase 9 / physiology*
  • Metallothionein 3
  • Phenotype
  • Phenylenediamines / pharmacology
  • Plant Proteins / pharmacology
  • Recombinant Proteins / metabolism
  • Time Factors
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Allergens
  • Antigens, CD34
  • Antigens, Plant
  • Metallothionein 3
  • Mt3 protein, mouse
  • Phenylenediamines
  • Plant Proteins
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Bet v 1 allergen, Betula
  • Bandrowski's base
  • Gelatinases
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9