Selectin-Binding Assay by Flow Cytometry

Methods Mol Biol. 2020:2132:111-118. doi: 10.1007/978-1-0716-0430-4_11.

Abstract

Cell-cell interactions mediated by selectins and their ligand glycans play pivotal roles in a variety of biological processes represented by leukocyte recruitment to inflammatory sites, lymphocyte homing, and extravasation of cancer cells. The interactions are enhanced at least partly through the upregulation of the selectin-ligand glycan expression, which is observed, for instance, during the activation of leukocytes or epithelial-mesenchymal transition of cancer cells. Selectin-binding assays such as cell adhesion assay or rolling assay have long been used to directly evaluate the activity of these cells in the selectin-mediated processes. In this chapter, we introduce a highly quantitative assay by flow cytometry using recombinant selectin-Ig(Fc) chimera proteins, showing our procedure and tips for E-selectin-binding assay of colon cancer cells undergoing epithelial-mesenchymal transition.

Keywords: Colon cancer; Epithelial-mesenchymal transition; Flow cytometry; Monoclonal antibody; Selectin; Selectin-Ig(Fc) chimera protein; Selectin-ligand glycan; Sialyl Lewis a; Sialyl Lewis x.

MeSH terms

  • Cell Adhesion
  • Cell Communication
  • Colonic Neoplasms / metabolism*
  • E-Selectin / genetics
  • E-Selectin / metabolism*
  • Epithelial-Mesenchymal Transition
  • Flow Cytometry
  • HT29 Cells
  • Humans
  • Immunoglobulin Fc Fragments / genetics*
  • Immunoglobulin Fc Fragments / metabolism
  • Polysaccharides / metabolism*
  • Protein Binding
  • Recombinant Fusion Proteins / metabolism

Substances

  • E-Selectin
  • Immunoglobulin Fc Fragments
  • Polysaccharides
  • Recombinant Fusion Proteins
  • SELE protein, human