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A bacterial E3 ubiquitin ligase IpaH9.8 targets NEMO/IKKgamma to dampen the host NF-kappaB-mediated inflammatory response.

Nature cell biology | Jan 22, 2010

http://www.ncbi.nlm.nih.gov/pubmed/20010814

NF-kappaB (nuclear factor kappaB) has a pivotal role in many cellular processes, including the inflammatory and immune responses and, therefore, its activation is tightly regulated by the IKK (IkappaB kinase) complex and by IkappaBalpha degradation. When Shigella bacteria multiply within epithelial cells they release peptidoglycans, which are recognized by Nod1 and stimulate the NF-kappaB pathway, thus leading to a severe inflammatory response. Here, we show that IpaH9.8, a Shigella effector possessing E3 ligase activity, dampens the NF-kappaB-mediated inflammatory response to the bacterial infection in a unique way. IpaH9.8 interacts with NEMO/IKKgamma and ABIN-1, a ubiquitin-binding adaptor protein, promoting ABIN-1-dependent polyubiquitylation of NEMO. Consequently, polyubiquitylated NEMO undergoes proteasome-dependent degradation, which perturbs NF-kappaB activation. As NEMO is essential for NF-kappaB activation, we propose that the polyubiquitylation and degradation of NEMO during Shigella infection is a new bacterial strategy to modulate host inflammatory responses.

Pubmed ID: 20010814 RIS Download

Mesh terms: Animals | Antigens, Bacterial | Bacterial Proteins | Cell Nucleus | Cells, Cultured | DNA-Binding Proteins | Female | Gene Expression Regulation | HeLa Cells | Humans | I-kappa B Kinase | Immunoprecipitation | Inflammation | Luciferases | Mice | Mice, Inbred C57BL | NF-kappa B | Pneumonia | RNA, Messenger | RNA, Small Interfering | Recombinant Proteins | Reverse Transcriptase Polymerase Chain Reaction | Two-Hybrid System Techniques | Ubiquitin | Ubiquitination

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Associated grants

  • Agency: NIDDK NIH HHS, Id: R01 DK071939
  • Agency: NIDDK NIH HHS, Id: R01 DK071939-07

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