Characterization and Activation of Fas Ligand-Producing Mouse B Cells and Their Killer Exosomes

Methods Mol Biol. 2021:2270:149-178. doi: 10.1007/978-1-0716-1237-8_9.

Abstract

B lymphocytes make several contributions to immune regulation including production of antibodies with regulatory properties, release of immune suppressive cytokines, and expression of death-inducing ligands. A role for Fas ligand (FasL)-expressing "killer" B cells in regulating T helper (TH) cell survival and chronic inflammation has been demonstrated in animal models of schistosome worm and other infections, asthma, autoimmune arthritis, and type 1 diabetes. FasL+ B cells were also capable of inducing immune tolerance in a male-to-female transplantation model. Interestingly, populations of B cells found in the spleen and lungs of naïve mice constitutively expresses FasL and have potent killer function against TH cells that is antigen-specific and FasL-dependent. Epstein-Barr virus-transformed human B cells constitutively express FasL and package it into exosomes that co-express MHC Class II molecules and have killer function against antigen-specific TH cells. FasL+ exosomes with markers of B-cell lineage are abundant in the spleen of naïve mice. Killer B cells therefore represent a novel target for immune modulation in many disease settings. Our laboratory has published methods of characterizing FasL+ B cells and inducing their proliferation in vitro. This updated chapter will describe methods of identifying and expanding killer B cells from mice, detecting FasL expression in B cells, extracting FasL+ exosomes from spleen and culture supernatants, and performing functional killing assays against antigen-specific TH cells.

Keywords: Apoptosis; B lymphocytes; Exosomes; Fas ligand; Immune regulation; Interleukin-10.

MeSH terms

  • Animals
  • Antigens / metabolism
  • Apoptosis / immunology
  • B-Lymphocytes / immunology
  • Cytokines / metabolism
  • Exosomes / metabolism*
  • Fas Ligand Protein / isolation & purification*
  • Fas Ligand Protein / metabolism
  • Female
  • Flow Cytometry / methods*
  • Histocompatibility Antigens Class II / metabolism
  • Immune Tolerance
  • Interleukin-10 / immunology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred DBA
  • Spleen / cytology
  • fas Receptor / metabolism

Substances

  • Antigens
  • Cytokines
  • Fas Ligand Protein
  • Histocompatibility Antigens Class II
  • fas Receptor
  • Interleukin-10