中华医学遗传学杂志
中華醫學遺傳學雜誌
중화의학유전학잡지
CHINESE JOURNAL OF MEDICAL GENETICS
2010年
6期
603-609
,共7页
陈志涛%夏冰%姜挺%周峰%邹开芳%葛柳青
陳誌濤%夏冰%薑挺%週峰%鄒開芳%葛柳青
진지도%하빙%강정%주봉%추개방%갈류청
细胞毒T淋巴细胞相关抗原4%溃疡性结肠炎%(AT)n重复序列%遗传多态性%表达
細胞毒T淋巴細胞相關抗原4%潰瘍性結腸炎%(AT)n重複序列%遺傳多態性%錶達
세포독T림파세포상관항원4%궤양성결장염%(AT)n중복서렬%유전다태성%표체
cytotoxic T-lymphocyte associated antigen 4%ulcerative colitis%(AT) n repeats%genetic polymorphism%expression
目的 研究细胞毒T淋巴细胞相关抗原4(cytotoxic T-lymphocyte associated antigen 4,CTLA-4)基因3'非转录区(AT)n重复序列多态性对溃疡性结肠炎(ulcerative colitis,UC)患者CTLA-4mRNA稳定性和基因表达的影响.方法 采用实时定量PCR方法检测膜型CTLA-4(full length CTLA-4,flCTLA-4)和可溶性CTLA-4(soluble CTLA-4,sCTLA-4)mRNA表达,半衰期法分析其mRNA稳定性.免疫组化检测flCTLA-4蛋白表达.酶联免疫吸附实验测定sCTLA-4蛋白水平.荧光PCR-毛细管电泳技术检测300例UC患者和700名健康对照者CTLA-4基因(AT)n重复序列多态性.结果 活动期UC患者肠黏膜sCTLA-4 mRNA的表达显著低于缓解期UC患者(P=0.004).在UC患者中,(AT)n重复序列长等位基因携带者表达低水平的flCTLA-4和sCTLA-4 mRNA以及sCTLA-4蛋白(均P<0.01).携带长等位基因的UC患者CTLA-4 mRNA的稳定性明显降低.UC患者CTLA-4基因(AT)n重复序列长等位基因携带者(≥116 bp)频率显著高于正常对照组(P<0.01),且与广泛型结肠炎相关(P=0.008).结论 UC患者CTLA-4基因(AT)n重复序列多态性与CTLA-4基因表达水平相关,携带(AT)n重复序列长等位基因的UC患者CTLA-4 mRNA及蛋白的表达降低,提示CTLA-4基因在UC遗传免疫发病机制中起重要作用.
目的 研究細胞毒T淋巴細胞相關抗原4(cytotoxic T-lymphocyte associated antigen 4,CTLA-4)基因3'非轉錄區(AT)n重複序列多態性對潰瘍性結腸炎(ulcerative colitis,UC)患者CTLA-4mRNA穩定性和基因錶達的影響.方法 採用實時定量PCR方法檢測膜型CTLA-4(full length CTLA-4,flCTLA-4)和可溶性CTLA-4(soluble CTLA-4,sCTLA-4)mRNA錶達,半衰期法分析其mRNA穩定性.免疫組化檢測flCTLA-4蛋白錶達.酶聯免疫吸附實驗測定sCTLA-4蛋白水平.熒光PCR-毛細管電泳技術檢測300例UC患者和700名健康對照者CTLA-4基因(AT)n重複序列多態性.結果 活動期UC患者腸黏膜sCTLA-4 mRNA的錶達顯著低于緩解期UC患者(P=0.004).在UC患者中,(AT)n重複序列長等位基因攜帶者錶達低水平的flCTLA-4和sCTLA-4 mRNA以及sCTLA-4蛋白(均P<0.01).攜帶長等位基因的UC患者CTLA-4 mRNA的穩定性明顯降低.UC患者CTLA-4基因(AT)n重複序列長等位基因攜帶者(≥116 bp)頻率顯著高于正常對照組(P<0.01),且與廣汎型結腸炎相關(P=0.008).結論 UC患者CTLA-4基因(AT)n重複序列多態性與CTLA-4基因錶達水平相關,攜帶(AT)n重複序列長等位基因的UC患者CTLA-4 mRNA及蛋白的錶達降低,提示CTLA-4基因在UC遺傳免疫髮病機製中起重要作用.
목적 연구세포독T림파세포상관항원4(cytotoxic T-lymphocyte associated antigen 4,CTLA-4)기인3'비전록구(AT)n중복서렬다태성대궤양성결장염(ulcerative colitis,UC)환자CTLA-4mRNA은정성화기인표체적영향.방법 채용실시정량PCR방법검측막형CTLA-4(full length CTLA-4,flCTLA-4)화가용성CTLA-4(soluble CTLA-4,sCTLA-4)mRNA표체,반쇠기법분석기mRNA은정성.면역조화검측flCTLA-4단백표체.매련면역흡부실험측정sCTLA-4단백수평.형광PCR-모세관전영기술검측300례UC환자화700명건강대조자CTLA-4기인(AT)n중복서렬다태성.결과 활동기UC환자장점막sCTLA-4 mRNA적표체현저저우완해기UC환자(P=0.004).재UC환자중,(AT)n중복서렬장등위기인휴대자표체저수평적flCTLA-4화sCTLA-4 mRNA이급sCTLA-4단백(균P<0.01).휴대장등위기인적UC환자CTLA-4 mRNA적은정성명현강저.UC환자CTLA-4기인(AT)n중복서렬장등위기인휴대자(≥116 bp)빈솔현저고우정상대조조(P<0.01),차여엄범형결장염상관(P=0.008).결론 UC환자CTLA-4기인(AT)n중복서렬다태성여CTLA-4기인표체수평상관,휴대(AT)n중복서렬장등위기인적UC환자CTLA-4 mRNA급단백적표체강저,제시CTLA-4기인재UC유전면역발병궤제중기중요작용.
Objective To investigate the effect of (AT)n repeat polymorphism of the 3'untranslated region in cytotoxic T-lymphocyte associated antigen 4 (CTLA-4)gene on CTLA-4 mRNA stability and full length (flCTLA-4) and soluble CTLA4 (sCTLA-4) expression in ulcerative colitis (UC). Methods flCTLA-4 mRNA in colonic biopsies and sCTLA-4 mRNA stability in peripheral blood mononuclear cells of UC patients were measured by quantitative PCR and half-life, respectively. The protein expression of flCTLA-4 in colonic biopsies and sCTLA-4 in sera of UC patients were determined by immunohistochemistry and enzyme-linked immunosorbent assay, respectively. The polymorphism of CTLA-4 (AT)n repeats in 300 UC and 700 age and sex matched healthy controls was genotyped by fluorescent PCR. Results Among the UC patients, sCTLA-4 mRNA expression levels were decreased in active disease compared to non-active disease (P=0. 004). Carriers of the longer alleles of the (AT)n repeats expressed lower levels of flCTLA-4 and sCTLA - 4 mRNA and sCTLA - 4 protein than those of the shorter alleles in UC (all P<0.01), and mRNA with long (AT)n repeat alleles has shorter half-life than mRNA with short alleles and, hence, are unstable. The frequency of long allele carriers of CTLA-4 (AT)n repeats was significantly higher in UC patients than in the healthy controls (22.0% vs. 6.3%, P<0.01, OR=4.21, 95% CI: 2.79-6.33), and associated with extensive colitis (P=0. 008). Conclusion CTLA-4 gene expression levels were associated with (AT)n repeat polymorphisms in UC patients. The expression of CTLA-4 mRNA and protein were decreased in carriers of the longer alleles of the (AT)n repeats of CTLA-4 gene. This study suggests that CTLA-4 plays an important role in genetic risk and pathophysiology for UC in central China.