Phorbol ester mediates reversible reduction of cloned T lymphocyte cytolysis.
Open Access
- 1 June 1983
- journal article
- research article
- Published by Oxford University Press (OUP) in The Journal of Immunology
- Vol. 130 (6) , 2499-2501
- https://doi.org/10.4049/jimmunol.130.6.2499
Abstract
Prolonged contact with nanomole to micromole concentrations of the tumor promoter phorbol myristate acetate causes a significant reduction in the lytic activity of cloned cytolytic T cells. Diminished lysis is apparent even in the presence of agglutinating lectins. PMA does not exert this effect by minimizing clone viability. In fact, these concentrations of PMA cause significant potentiation of antigen-driven proliferation for many of these same clones. The PMA-mediated loss of cytolysis is reversible. Although contact with antigen does not induce or enhance reexpression of cytolysis, PMA-treated cytolytic T cell clones display normal cytolytic activity after contact with lymphokines.This publication has 5 references indexed in Scilit:
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- Cytokine-dependent thymocyte responses. II. Generation of cytotoxic T lymphocytes from immature thymocytes.The Journal of Immunology, 1982
- Cytolytic T lymphocyte function is independent of growth phase and position in the mitotic cycleThe Journal of Experimental Medicine, 1981
- Alloreactive cloned T cell lines. I. Interactions between cloned amplifier and cytolytic T cell lines.The Journal of Experimental Medicine, 1980
- SIGNAL REQUIREMENTS FOR LYMPHOCYTE-T ACTIVATION .1. REPLACEMENT OF MACROPHAGE FUNCTION WITH PHORBOL MYRISTIC ACETATE1979