Expression of perforin and serine esterases by human γ/δ T cells

Hirotaka Koizumi*, Chau Ching Liu, Li Mou Zheng, Sanjay V. Joag, Nancy K. Bayne, Joseph Holoshitz, John Ding E. Young

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

101 Scopus citations

Abstract

γ/δ T cells have recently been described in association with a number of disorders, including autoimmune diseases, γ/δ T cells are thought to play a cytotoxic role, but their mechanism of action is not known. Several granule mediators of cytotoxicity, including a pore-forming protein (perform), and a family of serine esterases, have been isolated from cytotoxic T lymphocytes (CTL), lymphokine-activated killer (LAK) cells, and natural killer (NK) cells. We demonstrate here that γ/δ T cells also express these mediators. Northern blots show that γ/δ T cells express perforin, serine esterase 1 (SE 1), and SE 2. Three polyclonal antisera - raised against murine perforin, a peptide composed of amino acids 1-34 of human perforin, and human perforin expressed in bacteria-all reacted with a 70-kD protein in γ/δ T cells on Western blots. Immunostaining with antiperforin antisera shows that primary γ/δ T cells also contain perforin. Electron microscopy reveals that the granules of γ/δ T cells resemble those of CTL, LAK, and NK cells. γ/δ T cells also resemble γ/δ cells in possessing inclusion bodies in their nuclei. These results imply that γ/δ T cells resemble other cytolytic lymphocytes in their mechanism of action.

Original languageEnglish
Pages (from-to)499-502
Number of pages4
JournalJournal of Experimental Medicine
Volume173
Issue number2
StatePublished - 1991
Externally publishedYes

Keywords

  • Blotting, Northern
  • Blotting, Western
  • Cytotoxicity, Immunologic
  • DNA Probes
  • Esterases
  • Fluorescent Antibody Technique
  • Human
  • Immunophenotyping
  • Killer Cells, Natural
  • Membrane Proteins
  • RNA
  • Receptors, Antigen, T-Cell
  • Receptors, Antigen, T-Cell, gamma-delta
  • Support, Non-U.S. Gov't
  • Support, U.S. Gov't, P.H.S.
  • T-Lymphocyte Subsets

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