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
相关论文
共 58 条
[11]   Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1q, 3q, and 4q:: Evidence for epistasis between 1p and IBD1 [J].
Cho, JH ;
Nicolae, DL ;
Gold, LH ;
Fields, CT ;
LaBuda, MC ;
Rohal, PM ;
Pickles, MR ;
Qin, L ;
Fu, YF ;
Mann, JS ;
Kirschner, BS ;
Jabs, EW ;
Weber, J ;
Hanauer, SB ;
Bayless, TM ;
Brant, SR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (13) :7502-7507
[12]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[13]  
Clay FE, 1996, HUM GENET, V97, P723
[14]   INTERLEUKIN-1 (IL-1) GENE-EXPRESSION, SYNTHESIS, AND EFFECT OF SPECIFIC IL-1 RECEPTOR BLOCKADE IN RABBIT IMMUNE-COMPLEX COLITIS [J].
COMINELLI, F ;
NAST, CC ;
CLARK, BD ;
SCHINDLER, R ;
LLERENA, R ;
EYSSELEIN, VE ;
THOMPSON, RC ;
DINARELLO, CA .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (03) :972-980
[15]   Interleukin-1 receptor antagonist: A ''novel'' acute phase protein with antiinflammatory activities [J].
Cominelli, F ;
Pizarro, TT .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (12) :2813-2813
[16]   RECOMBINANT INTERLEUKIN-1 RECEPTOR ANTAGONIST BLOCKS THE PROINFLAMMATORY ACTIVITY OF ENDOGENEOUS INTERLEUKIN-1 IN RABBIT IMMUNE COLITIS [J].
COMINELLI, F ;
NAST, CC ;
DUCHINI, A ;
LEE, M .
GASTROENTEROLOGY, 1992, 103 (01) :65-71
[17]   An analysis of linkage disequilibrium in the interleukin-1 gene cluster, using a novel grouping method for multiallelic markers [J].
Cox, A ;
Camp, NJ ;
Nicklin, MJH ;
di Giovine, FS ;
Duff, GW .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) :1180-1188
[18]  
Craggs A, 2001, SCAND J GASTROENTERO, V36, P1173
[19]  
DANIS VA, 1995, CLIN EXP IMMUNOL, V99, P303
[20]  
di Giovine FS, 2000, CYTOKINE MOL BIOL, P21