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LPS-induced TNF-alpha factor (LITAF)-deficient mice express reduced LPS-induced cytokine: Evidence for LITAF-dependent LPS signaling pathways.

Previously we identified a transcription factor, LPS-Induced TNF-alpha Factor (LITAF), mediating inflammatory cytokine expression in LPS-induced processes. To characterize the role of LITAF in vivo, we generated a macrophage-specific LITAF-deficient mouse (macLITAF(-/-)). Our data demonstrate that in macrophages (i) several cytokines (such as TNF-alpha, IL-6, sTNF-RII, and CXCL16) are induced at lower levels in macLITAF(-/-) compared with LITAF(+/+) control macrophages; (ii) macLITAF(-/-) mice are more resistant to LPS-induced lethality. To further identify LITAF signaling pathways, we tested mouse TLR-2(-/-), -4(-/-), and -9(-/-) and WT peritoneal macrophages exposed to LPS. Using these cells, we now show that LITAF expression can be induced after challenge either with LPS from Porphyromonas gingivalis via agonism at TLR-2, or with LPS from Escherichia coli via agonism at TLR-4, both requiring functional MyD88. We also show that, in response to LPS, the MyD88-dependent LITAF pathway differs from the NF-kappaB pathway. Furthermore, using a kinase array, p38alpha was found to mediate LITAF phosphorylation and the inhibition of p38alpha with a p38-specific inhibitor (SB203580) blocked LITAF nuclear translocation and reduced LPS-induced TNF-alpha protein levels. Finally, macLITAF(-/-) macrophages rescued by LITAF cDNA transfection restored levels of TNF-alpha similar to those observed in WT cells. We conclude that LITAF is an important mediator of the LPS-induced inflammatory response that can be distinguished from NF-kappaB pathway and that p38alpha is the specific kinase involved in the pathway linking LPS/MyD88/LITAF to TNF.

Pubmed ID: 16954198


  • Tang X
  • Metzger D
  • Leeman S
  • Amar S


Proceedings of the National Academy of Sciences of the United States of America

Publication Data

September 12, 2006

Associated Grants

  • Agency: NIDCR NIH HHS, Id: R01 DE014079
  • Agency: NIDCR NIH HHS, Id: R01 DE14079

Mesh Terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • Cytokines
  • Down-Regulation
  • Escherichia coli
  • Lipopolysaccharides
  • Macrophages
  • Mice
  • Mice, Mutant Strains
  • Myeloid Differentiation Factor 88
  • NF-kappa B
  • Nuclear Proteins
  • Phosphorylation
  • Porphyromonas gingivalis
  • Protein Transport
  • Shock, Septic
  • Signal Transduction
  • Toll-Like Receptors
  • Transcription Factors
  • Tumor Necrosis Factor-alpha
  • p38 Mitogen-Activated Protein Kinases