IL-2-R beta expression and function within resting CD8+ T cells preferentially segregate with the CD45R0+ subset

Eur Cytokine Netw. 1991 Nov-Dec;2(5):319-27.

Abstract

Human peripheral blood CD8+ T cells constitutively express a low level of IL-2-R beta chains which were shown in this study to be preferentially carried by the CD45R0+ subset. Such receptors can transduce signals for in vitro IL-2-induced cytolytic function and for the initiation of soluble anti-CD3 and IL-2-induced cell proliferation. Using these stimulation models, a comparison was made between the responsiveness of resting, small CD45R0+ and CD45RA+ subpopulations of CD8+ T cells, both of them being isolated by negative selection and rigorously depleted of monocytes and of IL-2-inducible non-MHC-restricted CTL. Strong proliferation was induced in CD8+/CD45R0+ cells in response to IL-2 and soluble anti-CD3 (each of these stimuli being by itself ineffective), while in contrast, CD8+/CD45RA+ cells manifested, in this system, little reactivity. Accordingly, no conversion to the CD45R0 phenotype occurred in single stained CD45RA+ T cells following their incubation with the stimuli. A similar restriction of reactivity to CD8+/CD45R0+ T cells was observed with respect to IL-2-induced targetable T cell cytotoxicity. The CTL activity induced by IL-2 alone occurred without cell division. In contrast, the additional increase in CTL activity occurring upon the synergistic actions of anti-CD3 mAb and IL-2 coincided with intense cell proliferation, with no generation of LAK activity. The inhibition exerted by anti-IL-2-R beta mAb in the cytolytic and the proliferative activities induced by these stimuli in resting CD8+/CD45R0+ T cells emphasizes the importance of constitutive IL-2-R beta chains in the biology of these cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / immunology*
  • Cell Cycle
  • Flow Cytometry
  • Fluorescent Antibody Technique
  • Histocompatibility Antigens / immunology*
  • Humans
  • Leukocyte Common Antigens
  • Membrane Glycoproteins / immunology*
  • Receptors, Interleukin-2 / metabolism
  • Receptors, Interleukin-2 / physiology*
  • Signal Transduction
  • T-Lymphocyte Subsets
  • T-Lymphocytes, Cytotoxic
  • T-Lymphocytes, Regulatory / metabolism*

Substances

  • Antigens, CD
  • Histocompatibility Antigens
  • Membrane Glycoproteins
  • Receptors, Interleukin-2
  • Leukocyte Common Antigens