NR4A orphan nuclear receptor family in peripheral blood eosinophils from patients with atopic dermatitis and apoptotic eosinophils in vitro

被引:15
作者
Kagaya, S
Hashida, R
Ohkura, N
Tsukada, T
Sugita, Y
Terakawa, M
Tsujimoto, G
Katsunuma, T
Akasawa, A
Matsumoto, K
Saito, H
机构
[1] Genox Res Inc, Chuo, Japan
[2] Natl Canc Res Inst, Tumor Endocrinol Project, Chuo, Japan
[3] Natl Res Inst Child Hlth & Dev, Dept Allergy & Immunol, Tokyo, Japan
[4] RIKEN, Yokohama Inst, Res Ctr Allergy & Immunol, Kanagawa, Japan
关键词
apoptosis; atopic dermatitis; CD30; eosinophil; gene expression; GeneChip; NR4A nuclear receptor family; NOR1; Nur77; Nurr1; real-time RT-PCR;
D O I
10.1159/000085430
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
To identify novel genes related to the clinical signs of atopic dermatitis (AD), differentially expressed genes were sought in peripheral blood eosinophils from both AD patients and healthy volunteers. RNA was prepared from eosinophils, expression of various genes was monitored using the Affymetrix GeneChip, and expression was quantified by real-time RT-PCR. Two genes, Nur77 and NOR1, members of NR4A orphan nuclear receptor family, were expressed at a significantly higher level in AD patients than in healthy volunteers. Expression of another gene in the NR4A receptor family, Nurr1, was also higher in AD patients than in healthy volunteers. When peripheral blood leukocytes from healthy volunteers were fractionated, NOR1 expression was highest in eosinophils, but expression of Nur77 and Nurr1 genes was not eosinophil-specific. Extremely intense apoptosis was induced in both eosinophils and an eosinophil cell line, AML14.3D10, by treatment with antibody (Ab) to both CD30 and Fas. Rapid expression of the genes for the NR4A receptor family was observed with anti-CD30 Ab treatment but not with anti-Fas Ab. The NR4A orphan nuclear receptor family gene expression and the subsequent eosinophil apoptosis were downregulated by the MAPK inhibitor, U0126. These results suggest that the expression of the NR4A receptor family genes through CD30 signaling may regulate eosinophil apoptosis in allergic conditions such as AD. Copyright (C) 2005 S. Karger AG, Basel.
引用
收藏
页码:35 / 44
页数:10
相关论文
共 49 条
[1]  
Aizawa S, 1997, J BIOL CHEM, V272, P2042
[2]   The Aml14 and Aml14.3D10 cell lines: A long-overdue model for the study of eosinophils and more [J].
Baumann, MA ;
Paul, CC .
STEM CELLS, 1998, 16 (01) :16-24
[3]   Elevated serum levels of soluble CD30 in patients with atopic dermatitis (AD) [J].
Bengtsson, A ;
Holm, L ;
Back, O ;
Fransson, J ;
Scheynius, A .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1997, 109 (03) :533-537
[4]   Soluble CD30 and cyclosporine in severe atopic dermatitis [J].
Caproni, M ;
Salvatore, E ;
Cardinali, C ;
Brazzini, B ;
Fabbri, P .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2000, 121 (04) :324-328
[5]   Functional redundancy of the Nur77 and Nor-1 orphan steroid receptors in T-cell apoptosis [J].
Cheng, LEC ;
Chan, FKM ;
Cado, D ;
Winoto, A .
EMBO JOURNAL, 1997, 16 (08) :1865-1875
[6]   Region-specific immediate-early gene expression following the administration of corticotropin-releasing hormone in virgin and lactating rats [J].
DaCosta, APC ;
Kampa, RJ ;
Windle, RJ ;
Ingram, CD ;
Lightman, SL .
BRAIN RESEARCH, 1997, 770 (1-2) :151-162
[7]   Induction of nuclear factor kappa B by the CD30 receptor is mediated by TRAF1 and TRAF2 [J].
Duckett, CS ;
Gedrich, RW ;
Gilfillan, MC ;
Thompson, CB .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (03) :1535-1542
[8]   CD30-dependent degradation of TRAF2: implications for negative regulation of TRAF signaling and the control of cell survival [J].
Duckett, CS ;
Thompson, CB .
GENES & DEVELOPMENT, 1997, 11 (21) :2810-2821
[9]   Mechanisms of eosinophil-associated inflammation [J].
Gleich, GJ .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2000, 105 (04) :651-663
[10]   Gene expression profiling in immune cells using Microarray [J].
Granucci, F ;
Castagnoli, PR ;
Rogge, L ;
Sinigaglia, F .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2001, 126 (04) :257-266