Abstract
NF-kappa B is an important regulator of immunity and inflammation, and its activation pathway has been studied extensively. The mechanisms that downregulate the activity of NF-kappa B have also received a lot of attention, particularly since its activity needs to be terminated to prevent chronic inflammation and subsequent tissue damage. The COMMD family has been identified as a new group of proteins involved in NF-kappa B termination. All ten COMMD members share the structurally conserved carboxy-terminal motif, the COMM domain, and are ubiquitously expressed. They seem to play distinct and non-redundant roles in various physiological processes, including NF-kappa B signaling. In this review, we describe the mechanisms and proteins involved in the termination of canonical NF-kappa B signaling, with a specific focus on the role of the COMMD family in the down-modulation of NF-kappa B. (C) 2013 Elsevier B.V. All rights reserved.
Original language | English |
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Pages (from-to) | 2315-2321 |
Number of pages | 7 |
Journal | Biochimica et biophysica acta-Molecular basis of disease |
Volume | 1832 |
Issue number | 12 |
DOIs | |
Publication status | Published - Dec-2013 |
Keywords
- Inflammation
- NF-kappa B
- COMMD family
- Scaffold
- Termination
- EPITHELIAL SODIUM-CHANNEL
- TUMOR-SUPPRESSOR GENE
- COPPER TOXICOSIS
- INFLAMMATORY DISEASES
- UBIQUITIN LIGASE
- DEFICIENT MICE
- MURR1
- ACTIVATION
- PHOSPHORYLATION
- EXPRESSION