Transforming growth factor-β2 polymorphisms are associated with childhood atopic asthma

被引:20
作者
Hatsushika, K.
Hirota, T.
Harada, M.
Sakashita, M.
Kanzaki, M.
Takano, S.
Doi, S.
Fujita, K.
Enomoto, T.
Ebisawa, M.
Yoshihara, S.
Sagara, H.
Fukuda, T.
Masuyama, K.
Katoh, R.
Matsumoto, K.
Saito, H.
Ogawa, H.
Tamari, M.
Nakao, A.
机构
[1] Univ Yamanashi, Fac Med, Dept Immunol, Yamanashi 4093898, Japan
[2] Univ Yamanashi, Fac Med, Dept Otorhinolaryngol Head & Neck Surg, Yamanashi 4093898, Japan
[3] SNP Res Ctr, Lab Genet Allerg Dis, Kanagawa, Japan
[4] Osaka Prefectural Med Ctr Resp & Allerg Dis, Osaka, Japan
[5] Shiga Univ Med Sci, Coll Nursing, Shiga, Japan
[6] Wakayama Med Ctr, Japanese Red Cross Soc, Dept Otorhinolaryngol, Wakayama, Japan
[7] Natl Sagamihara Hosp, Clin Res Ctr Allergy & Rheumatol, Kanagawa, Japan
[8] Univ Yamanashi, Fac Med, Dept Human Pathol, Yamanashi, Japan
[9] Natl Res Inst Child Hlth & Dev, Dept Allergy & Immunol, Tokyo, Japan
[10] Juntendo Univ, Sch Med, Atopy Res Ctr, Tokyo 113, Japan
关键词
association; asthma; linkage disequilibrium; polymorphism; TGF-beta; 2;
D O I
10.1111/j.1365-2222.2007.02768.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Transforming growth factor (TGF)-beta plays an important role in the regulation of airway inflammation and remodelling in asthma. Recent studies suggest that TGF-beta(2) is a predominant isoform expressed in severe asthma and it is also associated with airway remodelling. To determine whether the polymorphisms in TGF-beta(2) are associated with childhood atopic bronchial asthma in a Japanese population. We identified a total of eight polymorphisms and characterized the linkage disequilibrium (LD) mapping of the gene. Three variants in the promoter and 3'UTR were genotyped, and we conducted an association study of TGF-beta(2) (childhood atopic asthma n=297, normal controls n=555). An association analysis of these variants and an expression and functional analysis were performed. 3'UTR 94862T > A was found to be significantly associated with the risk of childhood atopic asthma (P=0.00041). The -109 -> ACAA ins promoter variant was also associated with the risk of childhood atopic asthma (P=0.0037). TGF-beta(2) expression was observed in both the normal and asthmatic bronchial epithelium, and both real-time PCR and an ELISA showed a significant basal and TGF-beta(1)-induced TGF-beta(2) expression in the bronchial epithelial cell line BEAS2B. Furthermore, the promoter variant -109 -> ACAA ins increased the TGF-beta(2) promoter-reporter activity in BEAS2B cells. Our data suggest that TGF-beta(2) may therefore be involved in the development of childhood atopic asthma by means of functional genetic polymorphism. The polymorphisms in TGF-beta(2) may become important information for asthma susceptibility in children.
引用
收藏
页码:1165 / 1174
页数:10
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