Evidence for involvement of beta-glucan-binding cell surface lectins in human natural killer cell function

Cell Immunol. 1994 Sep;157(2):393-402. doi: 10.1006/cimm.1994.1236.

Abstract

We have studied the effects of yeast cell wall derivatives (zymosan and particulate beta-glucan), on the cytolytic effector function of human natural killer cells. Both zymosan and particulate beta-glucan were found to inhibit the NK-cell-mediated killing of K562, Molt-4, U937, and HL60 tumor cells. Zymosan also inhibited the IL-2-dependent proliferation of NK cells, suggesting that some component of the yeast cell wall delivers a down-modulatory signal affecting multiple NK cell functions. NK cell surface molecules capable of binding both zymosan and Sepharose-immobilized pustulan (linear 1,6-beta-D-glucan, a carbohydrate component of zymosan and particulate beta-glucan) were identified in detergent lysates prepared from surface iodinated NK cells. Our results suggest that NK cells express cell surface beta-glucan-binding lectins that may contribute to NK-cell-mediated natural cytotoxicity.

Publication types

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

MeSH terms

  • Cell Wall / immunology
  • Cytotoxicity, Immunologic
  • Glucans / pharmacology*
  • Humans
  • Immunity, Cellular
  • In Vitro Techniques
  • Killer Cells, Natural / immunology*
  • Lectins
  • Lymphocyte Activation
  • Receptors, Immunologic / physiology
  • Yeasts / immunology
  • Zymosan / pharmacology

Substances

  • Glucans
  • Lectins
  • Receptors, Immunologic
  • Zymosan