NF-κB: An essential transcription factor in psoriasis

被引:371
作者
Goldminz, A. M. [1 ]
Au, S. C. [1 ]
Kim, N. [1 ]
Gottlieb, A. B. [1 ]
Lizzul, P. F. [1 ]
机构
[1] Tufts Med Ctr, Dept Dermatol, Boston, MA 02111 USA
关键词
NF-kappa B; Psoriasis; Inflammation; T-cells; Keratinocytes; TNF-alpha; HUMAN KERATINOCYTES; GENE-EXPRESSION; IN-VIVO; ASSOCIATION; ACTIVATION; ALPHA; SUSCEPTIBILITY; DIFFERENTIATION; MECHANISMS; RECEPTORS;
D O I
10.1016/j.jdermsci.2012.11.002
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Nuclear factor kappa B (NF-kappa B) is a protein transcription factor that orchestrates inflammation and other complex biological processes. It is a key regulatory element in a variety of immune and inflammatory pathways, in cellular proliferation and differentiation and in apoptosis. Therefore NF-kappa B is a crucial mediator involved in the pathogenesis of psoriasis. Psoriasis, an inflammatory dermatosis, is marked by elevated levels of active, phosphorylated NF-kappa B. Genomic studies have also linked psoriasis with mediators in the NF-kappa B pathway. NF-kappa B has been hypothesized to connect the altered keratinocyte and immune cell behavior that characterizes the psoriatic milieu. Several anti-psoriatic therapies, including tumor necrosis factor-alpha blockers and glucocorticoids, reduce active NF-kappa B levels and related downstream elements, and other biologics currently in development, including interleukin-17 blockers, may also target this pathway. Compounds that specifically target NF-kappa B signaling may be developed as novel therapeutics for chronic inflammatory disorders including psoriasis. However, chronic NF-kappa B inhibition could also result in immunodeficiencies. Therefore, a delicate balance must be found that maximizes therapeutic potential while limiting harmful effects, and may be achieved through several possible approaches, including localized therapy, selective inhibition of NF-kappa B signaling in pathologic cells, incomplete pathway inhibition or short treatment durations. (c) 2012 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:89 / 94
页数:6
相关论文
共 50 条
[1]
Evaluation of survivin and NF-κB in psoriasis, an immunohistochemical study [J].
Abdou, Asmaa Gaber ;
Hanout, Hayam Mohamed .
JOURNAL OF CUTANEOUS PATHOLOGY, 2008, 35 (05) :445-451
[2]
The role of endothelial cell apoptosis in the effect of etanercept in psoriasis [J].
Avramidis, G. ;
Krueger-Krasagakis, S. ;
Krasagakis, K. ;
Fragiadaki, I. ;
Kokolakis, G. ;
Tosca, A. .
BRITISH JOURNAL OF DERMATOLOGY, 2010, 163 (05) :928-934
[3]
Discovering NF-κB [J].
Baltimore, David .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2009, 1 (01) :a000026
[4]
Begon E, 2007, EUR J DERMATOL, V17, P497
[5]
BAFF-induced NEMO-independent processing of NF-κB2 in maturing B cells [J].
Claudio, E ;
Brown, K ;
Park, S ;
Wang, HS ;
Siebenlist, U .
NATURE IMMUNOLOGY, 2002, 3 (10) :958-965
[6]
The lymphotoxin-β receptor induces different patterns of gene expression via two NF-κB pathways [J].
Dejardin, E ;
Droin, NM ;
Delhase, M ;
Haas, E ;
Cao, YX ;
Makris, C ;
Li, ZW ;
Karin, M ;
Ware, CF ;
Green, DR .
IMMUNITY, 2002, 17 (04) :525-535
[8]
ENK CD, 1995, J IMMUNOL, V154, P4851
[9]
Dithranol upregulates IL-10 receptors on the cultured human keratinocyte cell line HaCaT [J].
Farkas, A ;
Kemény, L ;
Szöny, BJ ;
Bata-Csörgö, Z ;
Pivarcsi, A ;
Kiss, M ;
Széll, M ;
Koreck, A ;
Dobozy, A .
INFLAMMATION RESEARCH, 2001, 50 (01) :44-49
[10]
Normal epidermal differentiation but impaired skin-barrier formation upon keratinocyte-restricted IKK1 ablation [J].
Gareus, Ralph ;
Huth, Marion ;
Breiden, Bernadette ;
Nenci, Arianna ;
Rosch, Nora ;
Haase, Ingo ;
Bloch, Wilhelm ;
Sandhoff, Konrad ;
Pasparakis, Manolis .
NATURE CELL BIOLOGY, 2007, 9 (04) :461-U185