Modulation of human monocyte functions by Fc fragments of IgG: a comparison to other monocyte 'activators'

Immunology. 1980 Sep;41(1):217-25.

Abstract

Human monocytes were maintained in tissue culture and the effect of various stimuli on their morphology and capacity to synthesize and secrete total protein, lysozyme, acid phosphatase, prostaglandin E and the second component of complement were determined. Human monomeric IgG, Fab fragments and albumin had no effect on the secretion of these products. However, addition of Fc fragments significantly decreased the synthesis of both lysosomal enzymes and the second component of complement and increased production of prostaglandin E. The addition of Con A to the monocyte monolayers resulted in a similar response. Latex particles slightly increased the secretion of acid phosphatase and C2, but had no effect on lysozyme secretion. Fc fragments also stimulated protein synthesis by monocyte monolayers cultured in serum-free medium. These 'activators' and endotoxin- or antigen-activated mononuclear cell supernatants (AMNS) resulted in varying degrees of increased spreading and adherence of the monocytes. The results of these studies suggest that the molecular species inducing the 'activated state' qualitatively and quantitatively determines the characteristics of the secretory response.

Publication types

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

MeSH terms

  • Acid Phosphatase / blood
  • Blood Proteins / biosynthesis
  • Cell Adhesion
  • Cells, Cultured
  • Complement C2 / biosynthesis
  • Humans
  • Immunoglobulin Fc Fragments / immunology
  • Immunoglobulin G / immunology*
  • Monocytes / immunology*
  • Monocytes / metabolism
  • Muramidase / blood
  • Prostaglandins E / biosynthesis

Substances

  • Blood Proteins
  • Complement C2
  • Immunoglobulin Fc Fragments
  • Immunoglobulin G
  • Prostaglandins E
  • Acid Phosphatase
  • Muramidase