Journal
IMMUNOLOGICAL REVIEWS
Volume 246, Issue -, Pages 346-358Publisher
WILEY
DOI: 10.1111/j.1600-065X.2012.01109.x
Keywords
IKK; NF-?B signaling; chronic inflammation; mouse models; inflammatory bowel disease; psoriasis; TNF
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Funding
- Deutsche Forschungsgemeinschaft [SFB 670, SFB829, CECAD]
- European Commission [INFLA-CARE]
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Since its discovery, nuclear factor-?B (NF-?B) has been recognized as a critical regulator of immune responses. While early studies focused on studying the role of NF-?B in the development and function of immune cells, more recently the function of the inhibitor of NF-?B kinase (IKK)/NF-?B pathway in non-immune cells has gained increased attention. Studies in genetic mouse models were instrumental in dissecting the cell-specific functions of NF-?B and provided experimental evidence that NF-?B signaling in epithelial cells is important for the maintenance of immune homeostasis in barrier tissues such as the skin and the intestine. Increased activation of IKK/NF-?B triggered cytokine expression by the epithelial cells, resulting in exacerbated tissue inflammatory responses. NF-?B inhibition in keratinocytes triggered severe tumor necrosis factor-dependent skin inflammation and epidermal hyperplasia, while inhibition of IKK/NF-?B signaling in intestinal epithelial cells disturbed the intestinal barrier and triggered severe chronic colon inflammation. Therefore, epithelial NF-?B signaling performs critical peace keeping functions in barrier tissues at the interface with the environment by regulating cell survival, barrier integrity, and the immunological and anti-microbial responses of epithelial cells. Improved understanding of epithelial NF-?B functions may hold the key for elucidating the etiology and pathophysiology of chronic inflammatory diseases in epithelial tissues.
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