A defect in nucleosome remodeling prevents IL-12(p35) gene transcription in neonatal dendritic cells

J Exp Med. 2004 Apr 5;199(7):1011-6. doi: 10.1084/jem.20031272. Epub 2004 Mar 29.

Abstract

To gain insight into the inability of newborns to mount efficient Th1 responses, we analyzed the molecular basis of defective IL-12(p35) expression in human neonatal monocyte-derived dendritic cells (DCs). Determination of IL-12(p35) pre-mRNA levels by real-time RT-PCR revealed that transcriptional activation of the gene in lipopolysaccharide-stimulated neonatal DCs was strongly impaired compared with adult DCs. We next showed that p50/p65 and p65/p65 dimers interact with kB#1 site, a critical cis-acting element of the IL-12(p35) promoter. We found that LPS-induced p65 activation was similar in adult and newborn DCs. Likewise, in vitro binding activity to the Sp1#1 site, previously shown to be critical for IL-12(p35) gene activation, did not differ in adults and newborns. Since the accessibility to this Sp1#1 site was found to depend on nucleosome remodeling, we used a chromatin accessibility assay to compare remodeling of the relevant nucleosome (nuc-2) in adult and neonatal DCs. We observed that nuc-2 remodeling in neonatal DCs was profoundly impaired in response to lipopolysaccharide. Both nuc-2 remodeling and IL-12(p35) gene transcription were restored upon addition of recombinant interferon-gamma. We conclude that IL-12(p35) transcriptional repression in neonatal DCs takes place at the chromatin level.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Base Sequence
  • Chromatin Assembly and Disassembly / drug effects
  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism*
  • Humans
  • In Vitro Techniques
  • Infant, Newborn
  • Interferon-gamma / pharmacology
  • Interleukin-12 / genetics*
  • Interleukin-12 Subunit p35
  • Lipopolysaccharides / pharmacology
  • NF-kappa B / metabolism
  • Nucleosomes / drug effects
  • Nucleosomes / metabolism*
  • Protein Subunits / genetics*
  • RNA Precursors / genetics
  • RNA Precursors / metabolism
  • Recombinant Proteins
  • Sp1 Transcription Factor / metabolism
  • Transcription, Genetic / drug effects

Substances

  • IL12A protein, human
  • Interleukin-12 Subunit p35
  • Lipopolysaccharides
  • NF-kappa B
  • Nucleosomes
  • Protein Subunits
  • RNA Precursors
  • Recombinant Proteins
  • Sp1 Transcription Factor
  • Interleukin-12
  • Interferon-gamma