Functional correlates of the interleukin-1 receptor antagonist gene polymorphism in the colonic mucosa in ulcerative colitis

被引:41
作者
Carter, MJ
Jones, S
Camp, NJ
Cox, A
Mee, J
Warren, B
Duff, GW
Lobo, AJ
di Giovine, FS
机构
[1] Univ Sheffield, Royal Hallamshire Hosp, Gastroenterol & Liver Unit, Sheffield S10 2JF, S Yorkshire, England
[2] Univ Sheffield, Royal Hallamshire Hosp, Div Genom Med, Sheffield S10 2JF, S Yorkshire, England
[3] John Radcliffe Hosp, Dept Histopathol, Oxford OX3 9DU, England
[4] Univ Utah, Sch Med, Salt Lake City, UT 84112 USA
关键词
interleukin-1 receptor antagonist; cytokines; inflammatory bowel disease; ulcerative colitis; genetics;
D O I
10.1038/sj.gene.6364032
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Association studies have identified the interleukin-1 receptor antagonist gene allele 2(IL-1RN*2) as a marker of susceptibility in ulcerative colitis (UC). This study investigated the significance of the IL-1RN genotype with respect to protein and mRNA expression in the colonic mucosa. Homogenates of rectal biopsies from 99 UC and 54 controls were assayed for cytokines IL-1ra, IL-1a and IL-1b using ELISA. IL1RN, IL1A and IL1B genotypes were determined using restriction-enzyme analysis. The ability of the two IL1RN alleles to generate steady-state mRNA accumulation was assessed in the colonic mucosa of seven heterozygous patients. Stepwise linear regression demonstrated that IL-1RN genotype (P=0.001), diagnosis (P<0.0001) and treatment (P<0.03) were independent factors associated with the IL-1ra protein level whilst IL1RN genotype (P=.005) and macroscopic inflammatory grade (P<.0001) were associated with the IL-1ra/total IL-1 ratio. The IL1RN*2 correlated with reduced IL-1ra and IL-1ra/IL-1 ratio with a gene dosage effect. In heterozygous UC patients the ratio of allele 1 mRNA/allele 2 steady state mRNA was always greater than 1 (range: 1.2-3.1) (P=.018). The IL-1RN*2 is associated with reduced levels of IL-1ra protein and IL-1RN mRNA in the colonic mucosa, providing a biologically plausible explanation for the observed association of the allele with the disease.
引用
收藏
页码:8 / 15
页数:8
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