Peroxisome proliferator-activated receptor α, δ, γ1 and γ2 expressions are present in human monocyte-derived dendritic cells and modulate dendritic cell maturation by addition of subtype-specific ligands

被引:41
作者
Jakobsen, MA
Petersen, RK
Kristiansen, K
Lange, M
Lillevang, ST
机构
[1] Odense Univ Hosp, Dept Clin Immunol, DK-5000 Odense C, Denmark
[2] Univ So Denmark, Dept Biochem & Mol Biol, Odense, Denmark
关键词
D O I
10.1111/j.1365-3083.2006.01745.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It has recently been shown by Chang et al. (J Immunol 2000;165:3584-91) that the maturation of dendritic cells (DC) in the presence of long-chain fatty acids redirects DC into Th0/Th2-inducing cells suggesting the involvement of a receptor for long-chain fatty acids like members of the peroxisome proliferator-activated receptors (PPAR) superfamily. Here, we show that immature and mature monocyte-derived DC (Mo-DC) express PPAR alpha, PPAR delta, PPAR gamma 1 and PPAR gamma 2 mRNA with the highest level of PPAR gamma 1 mRNA. We were only able to observe the expression of PPAR gamma 1 protein by Western blotting probably because the protein level of the other subtypes is below the detection limit. Synthetic ligands specific for PPAR alpha, PPAR delta or PPAR gamma added at day 0-6 have similar effect on the maturation of Mo-DC driving the maturation of Mo-DC with atypical phenotype, reduced expression of IL-10, IL-12 p35 and IL-12 p40 mRNA and with reduced stimulatory effects in mixed leucocyte reaction (MLR). Our data suggest that naturally occurring PPAR ligands like fatty acids and fatty acid derivates have anti-inflammatory effects by redirecting DC into a less stimulatory mode.
引用
收藏
页码:330 / 337
页数:8
相关论文
共 45 条
[11]   Sensing environmental lipids by dendritic cell modulates its function [J].
Coutant, F ;
Agaugué, S ;
Perrin-Cocon, L ;
André, P ;
Lotteau, V .
JOURNAL OF IMMUNOLOGY, 2004, 172 (01) :54-60
[12]   Peroxisome proliferator-activated receptor α negatively regulates the vascular inflammatory gene response by negative cross-talk with transcription factors NF-κB and AP-1 [J].
Delerive, P ;
De Bosscher, K ;
Besnard, S ;
Vanden Berghe, W ;
Peters, JM ;
Gonzalez, FJ ;
Fruchart, JC ;
Tedgui, A ;
Haegeman, G ;
Staels, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (45) :32048-32054
[13]   Peroxisome proliferator-activated receptor γ activators inhibit interleukin-12 production in murine dendritic cells [J].
Faveeuw, C ;
Fougeray, S ;
Angeli, V ;
Fontaine, J ;
Chinetti, G ;
Gosset, P ;
Delerive, P ;
Maliszewski, C ;
Capron, M ;
Staels, B ;
Moser, M ;
Trottein, F .
FEBS LETTERS, 2000, 486 (03) :261-266
[14]  
Gosset P, 2001, EUR J IMMUNOL, V31, P2857, DOI 10.1002/1521-4141(2001010)31:10<2857::AID-IMMU2857>3.0.CO
[15]  
2-X
[16]   Synergistic regulation of the human interleukin-12 p40 promoter by NFκB and Ets transcription factors in Epstein-Barr virus-transformed B cells and macrophages [J].
Gri, G ;
Savio, D ;
Trinchieri, G ;
Ma, XJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (11) :6431-6438
[17]   Activation of peroxisome proliferator-activated receptor γ bypasses the function of the retinoblastoma protein in adipocyte differentiation [J].
Hansen, JB ;
Petersen, RK ;
Larsen, BM ;
Bartkova, J ;
Alsner, J ;
Kristiansen, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (04) :2386-2393
[18]   PPAR-γ agonists inhibit production of monocyte inflammatory cytokines [J].
Jiang, CY ;
Ting, AT ;
Seed, B .
NATURE, 1998, 391 (6662) :82-86
[19]  
Kalinski P, 1997, J IMMUNOL, V159, P28
[20]   Commensal anaerobic gut bacteria attenuate inflammation by regulating nuclear-cytoplasmic shuttling of PPAR-γ and RelA [J].
Kelly, D ;
Campbell, JI ;
King, TP ;
Grant, G ;
Jansson, EA ;
Coutts, AGP ;
Pettersson, S ;
Conway, S .
NATURE IMMUNOLOGY, 2004, 5 (01) :104-112