Increased production of interleukin 6 and interleukin 8 in scleroderma fibroblasts

被引:77
作者
Kadono, T
Kikuchi, K
Ihn, H
Takehara, K
Tamaki, K
机构
[1] Univ Tokyo, Fac Med, Dept Dermatol, Bunkyo Ku, Tokyo 113, Japan
[2] Kanazawa Univ, Sch Med, Dept Dermatol, Kanazawa, Ishikawa 920, Japan
关键词
systemic sclerosis; reverse transcriptase polymerase chain reaction;
D O I
10.1016/S0923-1811(98)84143-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To determine additional abnormal characteristics related to cytokines in fibroblasts derived from systemic sclerosis (SSc), we examined the production of interleukin 6 (IL-6) and IL-8 and their mRNA levels both in scleroderma fibroblasts and in those from normal skin. Methods, Cultured fibroblasts from patients with SSc and healthy controls were examined. Production of IL-6 and IL-8 was assessed by specific ELISA, and the levels of IL-6 and IL-8 mRNA were determined by reverse transcriptase polymerase chain reaction (RT-PCR), Results. Basal production of both IL-6 and IL-S was significantly increased in scleroderma fibroblasts compared with controls. When cells were stimulated with either IL-1 beta (50 pg/ml) or tumor necrosis factor-alpha (TNF-alpha: 10 ng/ml), the production of IL-6 and IL-8 was predominantly increased in both cell strains and there was no significant difference in the production of IL-6 and IL-8 between them, When normal fibroblasts were stimulated with IL-IB for 48 h and subcultured, both IL-6 and IL-8 production were significantly increased, and production remained elevated even after 3 passages. RT-PCR revealed that IL-6 and IL-8 mRNA were detected in scleroderma fibroblasts but not in normal skin fibroblasts without cytokine stimulation, When stimulated with IL-1 beta, both cell strains expressed IL-6 and IL-8 mRNA to almost the same extent, Conclusion. Increased production of IL-6 and IL-8 by scleroderma fibroblasts suggests that these cells may have been stimulated by certain cytokines in vivo.
引用
收藏
页码:296 / 301
页数:6
相关论文
共 32 条
[1]   NEUTROPHIL-ACTIVATING PEPTIDE-1 INTERLEUKIN-8, A NOVEL CYTOKINE THAT ACTIVATES NEUTROPHILS [J].
BAGGIOLINI, M ;
WALZ, A ;
KUNKEL, SL .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (04) :1045-1049
[2]   PHAGOCYTOSING NEUTROPHILS PRODUCE AND RELEASE HIGH AMOUNTS OF THE NEUTROPHIL-ACTIVATING PEPTIDE-1/INTERLEUKIN-8 [J].
BAZZONI, F ;
CASSATELLA, MA ;
ROSSI, F ;
CESKA, M ;
DEWALD, B ;
BAGGIOLINI, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (03) :771-774
[3]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[4]   STIMULATION OF COLLAGEN AND GLYCOSAMINOGLYCAN PRODUCTION IN CULTURED HUMAN ADULT DERMAL FIBROBLASTS BY RECOMBINANT HUMAN INTERLEUKIN-6 [J].
DUNCAN, MR ;
BERMAN, B .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1991, 97 (04) :686-692
[5]  
ELIAS JA, 1990, J IMMUNOL, V145, P161
[6]  
ERCOLANI L, 1988, J BIOL CHEM, V263, P15335
[7]  
FEGHALI CA, 1992, J RHEUMATOL, V19, P1207
[8]   SCLERODERMA - A MODEL FOR FIBROSIS [J].
FLEISCHMAJER, R ;
PERLISH, JS ;
DUNCAN, M .
ARCHIVES OF DERMATOLOGY, 1983, 119 (12) :957-962
[10]  
GIERNE PA, 1989, J CLIN INVEST, V83, P585