Stimulated human melanocytes express and release interleukin-8, which is inhibited by luteolin: relevance to early vitiligo

被引:34
作者
Miniati, A. [1 ,2 ]
Weng, Z. [1 ,3 ]
Zhang, B. [1 ]
Therianou, A. [1 ,2 ]
Vasiadi, M. [1 ,3 ]
Nicolaidou, E. [2 ]
Stratigos, A. J. [2 ]
Antoniou, C. [2 ]
Theoharides, T. C. [1 ,3 ,4 ,5 ]
机构
[1] Tufts Univ, Sch Med, Dept Mol Physiol & Pharmacol, Mol Immunopharmacol & Drug Discovery Lab, Boston, MA 02111 USA
[2] Univ Athens, Sch Med, A Sygros Hosp, Dept Dermatol 1, GR-11527 Athens, Greece
[3] Tufts Univ, Sackler Sch Grad Biomed Sci, Grad Program Pharmacol & Expt Therapeut, Boston, MA 02111 USA
[4] Tufts Univ, Sch Med, Dept Biochem, Boston, MA 02111 USA
[5] Tufts Univ, Sch Med, Dept Internal Med, Boston, MA 02111 USA
基金
美国国家卫生研究院;
关键词
NECROSIS-FACTOR-ALPHA; UP-REGULATION; MAST-CELLS; SECRETION; DISEASE;
D O I
10.1111/ced.12164
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Vitiligo is a disorder of depigmentation, for which the pathogenesis is as yet unclear. Interleukin (IL)-8 (CXCL8) is a key inflammatory chemokine. We investigated the regulation of IL-8 production in human melanocytes, and the IL-8 serum levels and skin gene expression in patients with vitiligo and in controls. Cultured melanocytes were stimulated for 24h with tumour necrosis factor (TNF) 100ng/mL and IL-1 10ng/mL, with or without pretreatment with luteolin 50mol/L for 30min, and IL-8 release was measured by ELISA. Serum cytokines were measured by a microbead array. Skin biopsies were taken from healthy subjects (n=14) as well as from marginal lesional and nonlesional skin from patients with vitiligo (n=15). IL-8 gene expression was evaluated by quantitative real time PCR. Both TNF and IL-1 stimulated significant IL-8 release (P<0.01) from melanocytes, whereas pretreatment with luteolin significantly inhibited this effect (P<0.01). IL-8 gene expression was significantly increased in vitiligo compared with control skin (P<0.05). IL-8 may be involved in vitiligo inflammation. Inhibition by luteolin of IL-8 release could be useful for vitiligo therapy.
引用
收藏
页码:54 / 57
页数:4
相关论文
共 10 条
[1]   Increased angiogenesis and mast cells in the centre compared to the periphery of vitiligo lesions [J].
Aroni, K. ;
Voudouris, S. ;
Ioannidis, E. ;
Grapsa, A. ;
Kavantzas, N. ;
Patsouris, E. .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 2010, 302 (08) :601-607
[2]   Luteolin inhibits myelin basic protein-induced human mast cell activation and mast cell-dependent stimulation of Jurkat T cells [J].
Kempuraj, D. ;
Tagen, M. ;
Iliopoulou, B. P. ;
Clemons, A. ;
Vasiadi, M. ;
Boucher, W. ;
House, M. ;
Wolfberg, A. ;
Theoharides, T. C. .
BRITISH JOURNAL OF PHARMACOLOGY, 2008, 155 (07) :1076-1084
[3]  
LUGER TA, 1990, J INVEST DERMATOL, V95, P100
[4]  
Middleton E, 2000, PHARMACOL REV, V52, P673
[5]  
Mohler T, 1996, MELANOMA RES, V6, P307
[6]   Quercetin enhances melanogenesis by increasing the activity and synthesis of tyrosinase in human melanoma cells and in normal human melanocytes [J].
Nagata, H ;
Takekoshi, S ;
Takeyama, R ;
Homma, T ;
Osamura, RY .
PIGMENT CELL RESEARCH, 2004, 17 (01) :66-73
[7]  
Norgauer J, 2003, EUR J DERMATOL, V13, P124
[8]  
Schallreuter KU, 2008, EXP DERMATOL, V17, P139, DOI [10.1111/j.1600-0625.2007.00666_1.x, 10.1111/j.1600-0625.2007.00666.x]
[9]   Vitiligo-Inducing Phenols Activate the Unfolded Protein Response in Melanocytes Resulting in Upregulation of IL6 and IL8 [J].
Toosi, Siavash ;
Orlow, Seth J. ;
Manga, Prashiela .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2012, 132 (11) :2601-2609
[10]   Mitochondria Distinguish Granule-Stored from de novo Synthesized Tumor Necrosis Factor Secretion in Human Mast Cells [J].
Zhang, Bodi ;
Weng, Zuyi ;
Sismanopoulos, Nikolaos ;
Asadi, Sharhzad ;
Therianou, Anastasia ;
Alysandratos, Konstantinos-Dionysios ;
Angelidou, Asimenia ;
Shirihai, Orian ;
Theoharides, Theoharis C. .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2012, 159 (01) :23-32