Fibroblasts mediate T cell survival: a proposed mechanism for retention of primed T cells

J Exp Med. 1990 Dec 1;172(6):1873-6. doi: 10.1084/jem.172.6.1873.

Abstract

This report describes a salvage pathway whereby activated T lymphocytes revert to nonproliferating cells in the absence of antigen or mitogenic signals. After the removal of mitogenic cytokines, cultured T lymphocytes cease dividing and rapidly begin to undergo cell death. However, the addition of fibroblasts to interleukin 2 (IL-2)-propagated T cells results in prolonged survival of the previously activated T lymphocytes in the absence of proliferation. The prevention of cell death is also achieved by conditioned medium from the fibroblasts. T lymphocytes cultured with fibroblasts or the conditioned medium retain the ability to be restimulated if mitogenic stimuli are added to the culture. The activity is not accounted for by IL-1-7. The studies suggest a stromal cell-mediated, nonspecific mechanism for survival of primed T lymphocytes in a nonproliferating state.

Publication types

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

MeSH terms

  • Cell Survival* / drug effects
  • Cells, Cultured
  • Culture Media
  • Fibroblasts / cytology
  • Fibroblasts / physiology
  • Humans
  • Interleukin-2 / pharmacology
  • Interleukins / pharmacology*
  • Lymphocyte Activation
  • Synovial Membrane / pathology
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / physiology

Substances

  • Culture Media
  • Interleukin-2
  • Interleukins