Homeostatic T cell proliferation in a T cell-dendritic cell coculture system

Proc Natl Acad Sci U S A. 2002 Mar 5;99(5):2983-8. doi: 10.1073/pnas.052714199. Epub 2002 Feb 19.

Abstract

Naive T cells do not proliferate in normal individuals in the absence of antigen stimulation, but they proliferate spontaneously when T cells are severely depleted. We show here that coculture of syngeneic dendritic cells (DC) with naive T cells expressing a single T cell receptor also results in T cell proliferation in the absence of foreign antigen. As in lymphopenic mice, where T cell proliferation depends upon DC, this response in the coculture system requires interaction of the T cells' T cell receptor with self-peptide-MHCs on DC. This in vitro proliferation also requires soluble factors, including IL-15 secreted by DC, and can be inhibited potently by cell-cell contact with CD4+CD25+ regulatory T cells. The coculture system described may illuminate mechanisms that maintain stable numbers of T cells in normal individuals.

Publication types

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

MeSH terms

  • Animals
  • CD4-Positive T-Lymphocytes / metabolism
  • Cell Division
  • Coculture Techniques
  • Cytokines / metabolism
  • Dendritic Cells / metabolism*
  • Female
  • Homeodomain Proteins / genetics
  • Homeostasis
  • Interleukin-15 / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Receptors, Interleukin-2
  • Solubility
  • T-Lymphocytes / cytology*

Substances

  • Cytokines
  • Homeodomain Proteins
  • Interleukin-15
  • Receptors, Interleukin-2
  • RAG-1 protein