Involvement of the peripheral benzodiazepine receptor in the development of cutaneous pathology in Mrl/Lpr mice

被引:13
作者
Bribes, E [1 ]
Galiegue, S [1 ]
Bourrie, B [1 ]
Casellas, P [1 ]
机构
[1] Sanofi Synthelabo Rech, Immunol Oncol Dept, F-34184 Montpellier 04, France
关键词
Mrl/Lpr mice; PBR; skin lesion; SKIN-LESIONS; LUPUS-ERYTHEMATOSUS; PATHOGENESIS; EXPRESSION; APOPTOSIS; PROTECTION; INDUCTION; CELLS;
D O I
10.1016/S0165-2478(02)00177-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Mrl/Lpr mice develop inflammatory pathologies similar to human lupus erythematosus (LE). In that model, we showed a protective effect of different peripheral benzodiazepine receptor (PBR) ligands: PK 11195, Ro5-4864 and the newly described SSR180575 on the development of the cutaneous lesions. Specifically, we evidenced that a chronic treatment at 3 mg/kg per i.p. for 30 days prevented acanthosis, hyperkeratosis and generation of dermal infiltrates as compared with control untreated mice. In addition, using a specific polyclonal anti mouse PBR antibody, we characterized PBR expression in the skin lesions, and we observed that PBR expression in the epidermal component was increased when Mrl/Lpr mice developed the pathology and diminished upon PBR ligand treatment. PBR expression modulation together with the protective effects of its ligands further reinforce the role that PBR may play in the regulation of inflammation processes. Provided the exact mechanism of action that accounts for PBR action in that process is elucidated, these data support new therapeutic applications for specific potent PBR ligands. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:13 / 18
页数:6
相关论文
共 26 条
[1]
EXPRESSION OF DIAZEPAM-BINDING INHIBITOR PEPTIDE IN HUMAN SKIN - AN IMMUNOHISTOCHEMICAL AND ULTRASTRUCTURAL-STUDY [J].
ALHO, H ;
VAALASTI, A ;
PODKLETNOVA, I ;
RECHARDT, L .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1993, 101 (06) :800-803
[2]
BARTLETT RR, 1986, ARTICULAR CARTILAGE, P391
[3]
Ultraviolet light modulation of autoantigens, epidermal cytokines and adhesion molecules as contributing factors of the pathogenesis of cutaneous LE [J].
Bennion, S ;
Norris, DA .
LUPUS, 1997, 6 (02) :181-192
[4]
Involvement of peripheral benzodiazepine receptors in the protection of hematopoietic cells against oxygen radical damage [J].
Carayon, P ;
Portier, M ;
Dussossoy, D ;
Bord, A ;
Petitpretre, G ;
Canat, X ;
LeFur, G ;
Casellas, P .
BLOOD, 1996, 87 (08) :3170-3178
[5]
Ultraviolet Light-induced keratinocyte apoptosis: A potential mechanism for the induction of skin lesions and autoantibody production in LE [J].
CasciolaRosen, L ;
Rosen, A .
LUPUS, 1997, 6 (02) :175-180
[6]
Peripheral benzodiazepine receptors and mitochondrial function [J].
Casellas, P ;
Galiegue, S ;
Basile, AS .
NEUROCHEMISTRY INTERNATIONAL, 2002, 40 (06) :475-486
[7]
Apoptosis in the pathogenesis of cutaneous lupus erythematosus [J].
Chung, JH ;
Kwon, OS ;
Eun, HC ;
Youn, JI ;
Song, YW ;
Kim, JG ;
Cho, KH .
AMERICAN JOURNAL OF DERMATOPATHOLOGY, 1998, 20 (03) :233-241
[8]
RESPONSE OF CUTANEOUS LUPUS ERYTHEMATOSUS TO ULTRAVIOLET LIGHT [J].
EVERETT, MA ;
OLSON, RL .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1965, 44 (02) :133-&
[9]
FEINT H, 1996, J MED SOC NJ, V24, P226
[10]
SSR180575 (7-chloro-N,N,5-trimethyl-4-oxo-3-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-acetamide), a peripheral benzodiazepine receptor ligand, promotes neuronal survival and repair [J].
Ferzaz, B ;
Brault, E ;
Bourliaud, G ;
Robert, JP ;
Poughon, G ;
Claustre, Y ;
Marguet, F ;
Liere, P ;
Schumacher, M ;
Nowicki, JP ;
Fournier, J ;
Marabout, B ;
Sevrin, M ;
George, P ;
Soubrie, P ;
Benavides, J ;
Scatton, B .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 301 (03) :1067-1078