p100 Deficiency is insufficient for full activation of the alternative NF-κB pathway: TNF cooperates with p52-RelB in target gene transcription

PLoS One. 2012;7(8):e42741. doi: 10.1371/journal.pone.0042741. Epub 2012 Aug 6.

Abstract

Background: Constitutive activation of the alternative NF-κB pathway leads to marginal zone B cell expansion and disorganized spleen microarchitecture. Furthermore, uncontrolled alternative NF-κB signaling may result in the development and progression of cancer. Here, we focused on the question how does the constitutive alternative NF-κB signaling exert its effects in these malignant processes.

Methodology/principal findings: To explore the consequences of unrestricted alternative NF-κB activation on genome-wide transcription, we compared gene expression profiles of wild-type and NF-κB2/p100-deficient (p100(-/-)) primary mouse embryonic fibroblasts (MEFs) and spleens. Microarray experiments revealed only 73 differentially regulated genes in p100(-/-) vs. wild-type MEFs. Chromatin immunoprecipitation (ChIP) assays showed in p100(-/-) MEFs direct binding of p52 and RelB to the promoter of the Enpp2 gene encoding ENPP2/Autotaxin, a protein with an important role in lymphocyte homing and cell migration. Gene ontology analysis revealed upregulation of genes with anti-apoptotic/proliferative activity (Enpp2/Atx, Serpina3g, Traf1, Rrad), chemotactic/locomotory activity (Enpp2/Atx, Ccl8), and lymphocyte homing activity (Enpp2/Atx, Cd34). Most importantly, biochemical and gene expression analyses of MEFs and spleen, respectively, indicated a marked crosstalk between classical and alternative NF-κB pathways.

Conclusions/significance: Our results show that p100 deficiency alone was insufficient for full induction of genes regulated by the alternative NF-κB pathway. Moreover, alternative NF-κB signaling strongly synergized both in vitro and in vivo with classical NF-κB activation, thereby extending the number of genes under the control of the p100 inhibitor of the alternative NF-κB signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Embryo, Mammalian / cytology
  • Fibroblasts / metabolism
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Mice
  • NF-kappa B p52 Subunit / deficiency*
  • NF-kappa B p52 Subunit / metabolism
  • Phosphoric Diester Hydrolases / genetics
  • Promoter Regions, Genetic / genetics
  • Protein Binding
  • Signal Transduction*
  • Spleen / metabolism
  • Transcription Factor RelB / metabolism*
  • Transcription, Genetic*
  • Tumor Necrosis Factors / metabolism*

Substances

  • NF-kappa B p52 Subunit
  • Nfkb2 protein, mouse
  • Tumor Necrosis Factors
  • Transcription Factor RelB
  • Phosphoric Diester Hydrolases
  • alkylglycerophosphoethanolamine phosphodiesterase

Associated data

  • GEO/GSE30317

Grants and funding

This work was supported by funds from the Leibniz-Institute for Age Research - Fritz-Lipmann-Institute. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.