Phospholipase C treatment of certain human target cells reduces their susceptibility to NK lysis without affecting binding or sensitivity to lytic granules

Cell Immunol. 1991 Mar;133(1):127-37. doi: 10.1016/0008-8749(91)90185-e.

Abstract

Phosphatidylinositol-specific phospholipase C (PI-PLC) is an enzyme that has the capacity to release glycosyl-phosphatidyl inositol (G-PI)-anchored proteins from the cells surface. Pretreatment of the human T-cell leukemia cell line Molt-4 with PI-PLC resulted in a decrease in the susceptibility to lysis by natural killer (NK) cells. Treatment of the erythroleukemia cell line K562 with PI-PLC had no effect on its NK susceptibility. PI-PLC-treated and untreated Molt-4 bound equally well to lymphocytes in target-binding studies with effector cell preparations enriched for NK cells. Susceptibility to cytolytic granules isolated from rat LGL tumor cells remained the same after treatment of Molt-4 or K562 with PI-PLC. Combined treatment of Molt-4 with PI-PLC and rlFN-alpha or rlFN-gamma resulted in additive reductions of the NK susceptibility, suggesting that PI-PLC and interferons act on different mechanisms to protect cells from NK lysis. When expression of a number of antigens on Molt-4 and K562 was analyzed in flow cytometry, only the expression of CD58 was reduced after PI-PLC treatment. The susceptibility of Con A blasts to MLR derived cytotoxic T-cells was not altered by treatment with phospholipase. These data suggest that PI-PLC treatment reduces the capacity of some target cells to activate NK cells upon contract. The mechanism behind this phenomenon is presently unclear.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / analysis
  • Antigens, Differentiation / analysis
  • CD58 Antigens
  • Cell Line
  • Cytoplasmic Granules / enzymology
  • Cytotoxicity, Immunologic / drug effects*
  • Humans
  • Immunity, Innate / drug effects*
  • In Vitro Techniques
  • Interferon Type I / pharmacology
  • Interferon-gamma / pharmacology
  • Killer Cells, Natural / immunology*
  • Lymphocyte Activation
  • Signal Transduction / drug effects
  • T-Lymphocytes / immunology
  • Type C Phospholipases / pharmacology*

Substances

  • Antigens, CD
  • Antigens, Differentiation
  • CD58 Antigens
  • Interferon Type I
  • Interferon-gamma
  • Type C Phospholipases