Natural killer cells activate human dermal fibroblasts

Cytokine. 2000 Dec;12(12):1755-62. doi: 10.1006/cyto.2000.0787.

Abstract

Human dermal fibroblasts (HDF) undergo activation and secrete cytokines when cocultured with T cells. Here, we identify potent activators of HDF among human peripheral CD2(+)-lymphocytes. Populations with strong HDF activating capacity consisted essentially of cells with a natural killer (NK) surface marker phenotype (CD3(-), CD4(-), CD8(-), CD56(+)). Addition of these cells to HDF resulted in rapid increase of intracellular free calcium concentrations as an early rapid cell activation signal. Upregulation of mRNA encoding for the inflammatory cytokines IL-1 beta and IL-6 as well as for chemokines IL-8 and MCP-1 was detected after cells were cocultured. Elevated concentrations of IL-6 and IL-8 were found in coculture supernatants of HDF and NK-cells. Skin-homing NK cells leaving the blood-stream during an inflammatory skin reaction might therefore represent potent activators of local inflammatory cytokine and chemokine production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD2 Antigens / metabolism
  • CD3 Complex / metabolism
  • CD4 Antigens / metabolism
  • CD56 Antigen / metabolism
  • CD8 Antigens / metabolism
  • Calcium / metabolism
  • Calcium / pharmacology
  • Cell Count
  • Cell Division
  • Cell Membrane / metabolism
  • Chemokine CCL2 / metabolism
  • Coculture Techniques
  • Dose-Response Relationship, Drug
  • Enzyme-Linked Immunosorbent Assay
  • Fibroblasts / metabolism*
  • Flow Cytometry
  • Humans
  • Inflammation / metabolism
  • Interleukin-1 / metabolism
  • Interleukin-6 / metabolism
  • Interleukin-8 / metabolism
  • Killer Cells, Natural / metabolism*
  • Leukocytes, Mononuclear / metabolism
  • Microscopy, Fluorescence
  • Phenotype
  • RNA / metabolism
  • RNA, Messenger / metabolism
  • Time Factors
  • Up-Regulation

Substances

  • CD2 Antigens
  • CD3 Complex
  • CD4 Antigens
  • CD56 Antigen
  • CD8 Antigens
  • Chemokine CCL2
  • Interleukin-1
  • Interleukin-6
  • Interleukin-8
  • RNA, Messenger
  • RNA
  • Calcium