Inhibition of activated responses in dendritic cells exposed to lipopolysaccharide and lipoteichoic acid by diarylheptanoid oregonin

被引:10
作者
Choi, Eun Joo [1 ]
Ko, Hyun Hee [1 ]
Lee, Min Won [2 ]
Bang, Hyoweon [3 ]
Lee, Chung Soo [1 ]
机构
[1] Chung Ang Univ, Coll Med, Dept Pharmacol, Seoul 156756, South Korea
[2] Chung Ang Univ, Coll Pharm, Pharmacognosy Lab, Seoul 156756, South Korea
[3] Chung Ang Univ, Coll Med, Dept Physiol, Seoul 156756, South Korea
关键词
dendritic cells; cytokine production; change in cellular Ca2+ levels; oregonin; inhibitory effect;
D O I
10.1016/j.intimp.2008.01.024
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antigen-presenting dendritic cells may play an important role in the pathogenesis of inflammatory skin diseases, including atopic dermatitis. Oregonin is demonstrated to have anti-inflammatory and anti-oxidant effects. The present study was designed to assess the effect of oregonin against stimulated responses in dendritic cells of mouse bone marrow and spleen. Dendritic cells exposed to lipopolysaccharide, lipoteichoic acid and IL-1 beta exhibited increase in the production of IL-12 p70 and TNF-alpha, increase in the formation of reactive oxygen species and nitric oxide, and elevation of intracellular Ca2+ levels. Treatment of oregonin attenuated the microbial product- or IL-1 beta-stimulated responses in dendritic cells in a dose-dependent manner. Oregonin revealed a significant inhibitory effect on the production of cytokine, the formation of reactive oxygen species and nitric oxide, and the change in intracellular Ca2+ levels in dendritic cells of bone marrow and spleen. The results show that oregonin seems to attenuate the stimulated cell responses, including cytokine production, in dendritic cells exposed to microbial products and IL-1 beta. The findings suggest that oregonin may exert an inhibitory effect against the dendritic cell-mediated immune response. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:748 / 755
页数:8
相关论文
共 42 条
[1]   Cytokine production, activation marker, and skin homing receptor in children with atopic dermatitis and bronchial asthma [J].
Antúnez, C ;
Torres, MJ ;
Mayorga, C ;
Corzo, JL ;
Jurado, A ;
Santamaría-Babi, LF ;
Vera, A ;
Blanca, M .
PEDIATRIC ALLERGY AND IMMUNOLOGY, 2006, 17 (03) :166-174
[2]   Calcium signaling through phospholipase C activates dendritic cells to mature and is necessary for the activation and maturation of dendritic cells induced by diverse agonists [J].
Bagley, KC ;
Abdelwahab, SF ;
Tuskan, RG ;
Lewis, GK .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2004, 11 (01) :77-82
[3]   The role of microorganisms in atopic dermatitis [J].
Baker, BS .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2006, 144 (01) :1-9
[4]   Immunobiology of dendritic cells [J].
Banchereau, J ;
Briere, F ;
Caux, C ;
Davoust, J ;
Lebecque, S ;
Liu, YT ;
Pulendran, B ;
Palucka, K .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :767-+
[5]   Atopic dermatitis [J].
Boguniewicz, M ;
Leung, DYM .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2006, 117 (02) :S475-S480
[6]   Oxidants and asthma [J].
Caramori, G ;
Papi, A .
THORAX, 2004, 59 (02) :170-173
[7]   Origin, maturation and antigen presenting function of dendritic cells [J].
Cella, M ;
Sallusto, F ;
Lanzavecchia, A .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (01) :10-16
[8]   The cellular basis for diverse responses to oxygen [J].
Chandel, Navdeep S. ;
Budinger, G. R. Scott .
FREE RADICAL BIOLOGY AND MEDICINE, 2007, 42 (02) :165-174
[9]   Immune dysregulation in atopic dermatitis [J].
del Giudice, Michele Miraglia ;
Decimo, Fabio ;
Leonardi, Salvatore ;
Maioello, Nunzia ;
Amelio, Raffaele ;
Capasso, Antonella ;
Capristo, Carlo ;
Capristo, Angelo F. .
ALLERGY AND ASTHMA PROCEEDINGS, 2006, 27 (06) :451-455
[10]   Calcium and oxidative stress: from cell signaling to cell death [J].
Ermak, G ;
Davies, KJA .
MOLECULAR IMMUNOLOGY, 2002, 38 (10) :713-721