Human CD40-ligand: molecular cloning, cellular distribution and regulation of expression by factors controlling IgE

J F Gauchat1, J P Aubry, G Mazzei

  • 1Glaxo Institute for Molecular Biology, Plan les Ouates/Geneva, Switzerland.

FEBS Letters
|January 11, 1993
PubMed

Insights

Researchers cloned human CD40-Ligand (CD40-L) and found its expression on T cells, correlating with IgE production. Interleukin-4 increased CD40-L mRNA, while Interferon-gamma decreased it.

Area of Science:

  • Immunology
  • Molecular Biology

Background:

  • CD40-Ligand (CD40-L) is a crucial molecule in immune responses.
  • Understanding CD40-L expression is vital for immune system research.

Purpose of the Study:

  • To clone the cDNA for human CD40-Ligand (CD40-L).
  • To investigate the expression patterns of CD40-L in human peripheral blood mononuclear cells (PBMNC).
  • To explore the relationship between CD40-L expression and IgE production.

Main Methods:

  • Cloning of human CD40-L cDNA from a CD4-positive T cell clone.
  • Northern blot analysis to detect CD40-L mRNA.
  • Flow cytometry (FACS) analysis to determine CD40-L protein expression on different cell types.
  • Treatment of cells with Interleukin-4 (IL-4) and Interferon-gamma (IFN-γ) to assess their effects on CD40-L expression.

Main Results:

  • The deduced amino acid sequence predicted a type II membrane protein of 261 amino acids.
  • Human CD40-L was detected on T cells (both CD4+ and CD8+ subsets, including CD45R0+ and CD45RA+), but absent from B cells and monocytes.
  • IL-4 upregulated CD40-L mRNA levels, while IFN-γ reduced them.

Conclusions:

  • Human CD40-L is expressed on various T cell subsets.
  • The expression of CD40-L is modulated by cytokines involved in IgE regulation.
  • These findings suggest a correlation between human CD40-L expression and IgE production, highlighting its potential role in allergic responses.