Human mast cells release metalloproteinase-9 on contact with activated T cells: juxtacrine regulation by TNF-alpha

J Immunol. 2001 Oct 1;167(7):4008-16. doi: 10.4049/jimmunol.167.7.4008.

Abstract

Mast cells, essential effector cells in allergic inflammation, have been found to be activated in T cell-mediated inflammatory processes in accordance with their residence in close physical proximity to T cells. We have recently reported that mast cells release granule-associated mediators and TNF-alpha upon direct contact with activated T cells. This data suggested an unrecognized activation pathway, where mast cells may be activated during T cell-mediated inflammation. Herein, we show that this cell-cell contact results in the release of matrix metalloproteinase (MMP)-9 and the MMP inhibitor tissue inhibitor of metalloproteinase 1 from HMC-1 human mast cells or from mature peripheral blood-derived human mast cells. The expression and release of these mediators, as well as of beta-hexosaminidase and several cytokines, were also induced when mast cells were incubated with cell membranes isolated from activated, but not resting, T cells. Subcellular fractionation revealed that the mature form of MMP-9 cofractionated with histamine and tryptase, indicating its localization within the secretory granules. MMP-9 release was first detected at 6 h and peaked at 22 h of incubation with activated T cell membranes, while TNF-alpha release peaked after only 6 h. Anti-TNF-alpha mAb inhibited the T cell membrane-induced MMP-9 release, indicating a possible autocrine regulation of MMP release by mast cell TNF-alpha. This cascade of events, whereby mast cells are activated by T cells to release cytokines and MMP-9, which are known to be essential for leukocyte extravasation and recruitment to affected sites, points to an important immunoregulatory function of mast cells within the context of T cell-mediated inflammatory processes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • Autocrine Communication*
  • Cells, Cultured
  • Collagenases / analysis
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Enzyme Precursors / analysis
  • Humans
  • Jurkat Cells
  • Lymphocyte Activation
  • Mast Cells / enzymology
  • Mast Cells / immunology*
  • Matrix Metalloproteinase 9 / biosynthesis*
  • Matrix Metalloproteinase 9 / genetics
  • Models, Immunological
  • RNA, Messenger / biosynthesis
  • Secretory Vesicles / chemistry
  • T-Lymphocytes / immunology*
  • Tissue Inhibitor of Metalloproteinase-1 / biosynthesis
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / physiology*
  • beta-N-Acetylhexosaminidases / biosynthesis

Substances

  • Antibodies, Monoclonal
  • Cytokines
  • Enzyme Precursors
  • RNA, Messenger
  • Tissue Inhibitor of Metalloproteinase-1
  • Tumor Necrosis Factor-alpha
  • beta-N-Acetylhexosaminidases
  • Collagenases
  • pro-matrix metalloproteinase 9
  • Matrix Metalloproteinase 9