IL-12, STAT4-dependent up-regulation of CD4(+) T cell core 2 beta-1,6-n-acetylglucosaminyltransferase, an enzyme essential for biosynthesis of P-selectin ligands

J Immunol. 2001 Oct 15;167(8):4476-84. doi: 10.4049/jimmunol.167.8.4476.

Abstract

TCR activation of naive T cells in the presence of IL-12 drives polarization toward a Th1 phenotype and synthesis of P- and E-selectin ligands. Fucosyltransferase VII (Fuc-T VII) and core 2 beta-1,6-N-acetylglucosaminyltransferase (C2GnT) are critical for biosynthesis of selectin ligands. P-selectin glycoprotein ligand-1 is the best characterized ligand for P-selectin and also binds E-selectin. The contributions of TCR and cytokine signaling pathways to up-regulate Fuc-T VII and C2GnT during biosynthesis of E- and P-selectin ligands, such as P-selectin glycoprotein ligand 1, are unknown. IL-12 signals via the STAT4 pathway. Here, naive DO11.10 TCR transgenic and STAT4(-/-) TCR transgenic CD4(+) T cells were stimulated with Ag and IL-12 (Th1 condition), IL-4 (Th2), or neutralizing anti-IL-4 mAb only (Th0). The levels of Fuc-T VII and C2GnT mRNA in these cells were compared with their adhesive interactions with P- and E-selectin in vitro under flow. The data show IL-12/STAT4 signaling is necessary for induction of C2GnT, but not Fuc-TVII mRNA, and that STAT4(-/-) Th1 cells do not traffic normally to sites of inflammation in vivo, do not interact with P-selectin, and exhibit a partial reduction of E-selectin interactions under shear stress in vitro. Ag-specific TCR activation in CD4(+) T cells was sufficient to trigger induction of Fuc-TVII, but not C2GnT, mRNA and expression of E-selectin, but not P-selectin, ligands. Thus, Fuc-T VII and C2GnT are regulated by different signals during Th cell differentiation, and both cytokine and TCR signals are necessary for the expression of E- and P-selectin ligands.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • CD4-Positive T-Lymphocytes / drug effects*
  • CD4-Positive T-Lymphocytes / enzymology
  • Cell Adhesion
  • DNA-Binding Proteins / metabolism*
  • E-Selectin / metabolism
  • Fucosyltransferases / biosynthesis
  • Gene Expression Regulation
  • Interleukin-12 / pharmacology*
  • Ligands
  • Lymphocyte Activation
  • Membrane Glycoproteins / biosynthesis*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Mutant Strains
  • N-Acetylglucosaminyltransferases / biosynthesis*
  • P-Selectin / metabolism*
  • Receptors, Antigen, T-Cell / metabolism
  • STAT4 Transcription Factor
  • Trans-Activators / metabolism*
  • Up-Regulation

Substances

  • DNA-Binding Proteins
  • E-Selectin
  • Ligands
  • Membrane Glycoproteins
  • P-Selectin
  • P-selectin ligand protein
  • Receptors, Antigen, T-Cell
  • STAT4 Transcription Factor
  • Stat4 protein, mouse
  • Trans-Activators
  • Interleukin-12
  • Fucosyltransferases
  • N-Acetylglucosaminyltransferases
  • beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-acetylglucosaminyl transferase
  • galactoside 3-fucosyltransferase