A T cell surface molecule different from CD2 is involved in spontaneous rosette formation with erythrocytes

J Immunol. 1988 Mar 15;140(6):1802-7.

Abstract

Increasing evidence indicates that rosettes which spontaneously from between human T cells and E might be of physiologic relevance. We show here that another T cell-surface molecule than CD2 is involved in rosette formation. Four mAb have been obtained reacting with human T cells that block rosettes with E from many species, including autologous cells. They react with a molecule, we termed E2, which is actively synthetized by T and monocytic cells. Immunoprecipitation revealed a major 32-kDa band. Immunoblots revealed a major 32-kDa band and a minor 20-kDa band. This molecule was detected on all T cells tested--and present at high densities on corticothymocytes, but at low densities on medullary thymocytes. It was also found on monocytes but not on B cells. However B-CLL cells did carry this molecule. E2 molecules were also detected on nonhematologic cells. Together with the recent evidence that 3 molecules from the erythrocyte surface are also involved for rosettes, intricate molecular interactions would account for adhesion of T cells to autologous E and possibly autologous nucleated cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / immunology
  • B-Lymphocytes / analysis
  • CD2 Antigens
  • Carrier Proteins
  • Cell Adhesion
  • Erythrocytes / immunology
  • Humans
  • Leukemia, Lymphoid / pathology
  • Leukocytes, Mononuclear / analysis
  • Lymphocyte Activation
  • Membrane Glycoproteins / physiology*
  • Receptors, Immunologic
  • Rosette Formation*
  • T-Lymphocytes / classification
  • T-Lymphocytes / immunology*
  • Tumor Cells, Cultured / analysis

Substances

  • Antibodies, Monoclonal
  • CD2 Antigens
  • Carrier Proteins
  • Membrane Glycoproteins
  • Receptors, Immunologic