4.6 Article

Identification of tripartite motif-containing 22 (TRIM22) as a novel NF-κB activator

Journal

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2011.05.124

Keywords

TRIM22; NF-kappa B; Pro-inflammatory cytokine; PDTC

Funding

  1. National Natural Science Foundation of China [30890141, 81072428, 30872355]
  2. Shanghai STCSM [09JC1401800]
  3. Ministry of Education of China [2009071120060]
  4. Major State Basic Research Development Program of China [2007CB512401]
  5. Jiangsu provincial Basic Research Program (Innovation Scholars Climbing Program) [SBK201010093]
  6. Program for Outstanding Medical Academic Leader of Shanghai [LJ06011]

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Increasing evidence suggests that TRIM family proteins may play important roles in the regulation of innate immune signaling pathways. Here we report TRIM22 is involved in the activation of NF-kappa B. It was found that overexpression of TRIM22 could dose-dependently activate NF-kappa B as demonstrated by reporter gene assay and electrophoretic mobility shift assay, but had no effect on the activity of other transcription factors, including NF-AT, AP-1, C/EBP and IRFs. Further study showed that both the N-terminal RING domain and C-terminal SPRY domain were crucial for TRIM22-mediated NF-kappa B activation. Moreover, our results revealed that TRIM22 overexpression could significantly induce the secretion of pro-inflammatory cytokines by human macrophage cell line U937 in an NF-kappa B-dependent manner. These data suggested that TRIM22 was a positive regulator of NF-kappa B-mediated transcription. (C) 2011 Elsevier Inc. All rights reserved.

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