Simultaneous cytometric analysis for the expression of cytoplasmic and surface antigens in activated T cells

Cytometry. 1988 Jan;9(1):44-51. doi: 10.1002/cyto.990090108.

Abstract

A method of two-colour immunofluorescence staining has been developed to allow the simultaneous analysis of both surface and cytoplasmic antigens. This involves the use of direct fluorochrome antibody conjugates for cell-surface antigen staining, followed by cell permeabilization and the staining of cytoplasmic antigens with biotinylated antibodies and streptavidin-fluorochrome conjugates. Fluorochrome-antibody conjugates bound to cell-surface epitopes were found not to be affected by the subsequent permeabilisation and cytoplasmic staining. This method was used to examine the surface phenotype of T cells expressing a cytoplasmic antigen, STA. STA is a unique determinant detected in activated human T cells by the monoclonal antibody K-1-21, which also recognizes a cross-reactive conformation-dependent epitope on human free kappa light chains. Cytometric analysis showed that STA is found in both Leu 2a+ cytotoxic/suppressor T cells and Leu 3a+ helper/inducer T cells but is not induced in the Leu 15+ population which contains suppressor T cells. STA was also shown to be an activation antigen in murine T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens / analysis*
  • Antigens, Surface / analysis*
  • Antigens, Surface / immunology*
  • Cells, Cultured
  • Cytoplasm / immunology*
  • Flow Cytometry
  • Fluorescent Antibody Technique
  • Humans
  • Lymphocyte Activation
  • Methods
  • Mice
  • Phenotype
  • T-Lymphocytes / immunology
  • T-Lymphocytes / ultrastructure*
  • Thymus Gland / cytology
  • Tumor Necrosis Factor Receptor Superfamily, Member 7

Substances

  • Antigens
  • Antigens, Surface
  • Tumor Necrosis Factor Receptor Superfamily, Member 7