On the origin of the FcRIII (CD16)-containing vesicle population in human neutrophil granulocytes

Eur J Cell Biol. 1991 Apr;54(2):313-21.

Abstract

Human blood neutrophils bear two types of Fc receptors that recognize the Fc portion of immunoglobulin G: FcRII and FcRIII. In earlier studies we found that neutrophils not only express FcRIII on their plasma membrane but also contain a large population of FcRIII-containing vesicles mainly located in the juxtanuclear area. To find out whether these vesicles derive from the plasma membrane, we used electron microscopic techniques to study compartments involved in ligand-independent endocytosis in human neutrophil granulocytes. The endocytic compartments were labeled with BSA-gold. This marker entered the cell through non-coated invaginations of the plasma membrane as well as via coated pits. After internalization, BSA-gold was present in numerous electron-lucent vesicles in the juxtanuclear area and in the trans-Golgi reticulum, endosomes, and lysosome-like structures. FcRIII also occurred in the BSA-gold-containing electron-lucent vesicles in the juxtanuclear area, as shown by postembedding immunocytochemical labeling of FcRIII in cells already containing BSA-gold. Quantification showed that 29% of all FcRIII-containing vesicles also bear BSA-gold while the remaining 71% contain only the receptor. In sum, our findings show that one third of the FcRIII-containing electron-lucent vesicles in neutrophil granulocytes derive from the plasma membrane and are involved in ligand-independent endocytosis of FcRIII. The majority of these vesicles, however, are not of an endocytic origin and might constitute an "internal pool" of receptors in these cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal
  • Antigens, CD / metabolism*
  • Antigens, Differentiation / metabolism*
  • Endocytosis*
  • Endosomes / immunology*
  • Endosomes / ultrastructure
  • Golgi Apparatus / immunology
  • Golgi Apparatus / ultrastructure
  • Humans
  • Lysosomes / immunology
  • Lysosomes / ultrastructure
  • Microscopy, Immunoelectron
  • Neutrophils / immunology*
  • Neutrophils / ultrastructure
  • Receptors, Fc / metabolism*
  • Receptors, IgG
  • Vacuoles / immunology
  • Vacuoles / ultrastructure

Substances

  • Antibodies, Monoclonal
  • Antigens, CD
  • Antigens, Differentiation
  • Receptors, Fc
  • Receptors, IgG