中华皮肤科杂志
中華皮膚科雜誌
중화피부과잡지
Chinese Journal of Dermatology
2008年
10期
677-679
,共3页
胡勇%郭庆%曾凡钦%唐增奇%林燕辉%汤红峰
鬍勇%郭慶%曾凡欽%唐增奇%林燕輝%湯紅峰
호용%곽경%증범흠%당증기%림연휘%탕홍봉
尖锐湿疣%转化生长因子β%潜在性TGFβ结合蛋白质类%受体,转化生长因子
尖銳濕疣%轉化生長因子β%潛在性TGFβ結閤蛋白質類%受體,轉化生長因子
첨예습우%전화생장인자β%잠재성TGFβ결합단백질류%수체,전화생장인자
Condyloma acuminatum%Transforming growth factor beta%Latent TGF-beta binding proteins%Receptor,transforming growth factors
目的 探讨潜在结合蛋白(LTaP)-1及其Ⅱ型受体(TGF-βRⅡ)与尖锐湿疣发病的相关性. 方法 采用实时荧光定量PCR技术和SP免疫组化技术分别检测30例CA皮损及17例正常包皮组织中LTBP和TGF-βRⅡ的mRNA和蛋白的表达. 结果 CA皮损中LTBP-1及TGF-βRⅡ的mRNA的表达水平均低于对照组包皮组织(2-△△α2).免疫组化结果显示:LTBP-1和TGF-βRⅡ的染色强度较正常人包皮组织降低,差异有统计学意义(P<0.01). 结论 LTBP-1和TGF-βRⅡ的表达下调,可导致TCF-β活化及信号转导通路的异常.
目的 探討潛在結閤蛋白(LTaP)-1及其Ⅱ型受體(TGF-βRⅡ)與尖銳濕疣髮病的相關性. 方法 採用實時熒光定量PCR技術和SP免疫組化技術分彆檢測30例CA皮損及17例正常包皮組織中LTBP和TGF-βRⅡ的mRNA和蛋白的錶達. 結果 CA皮損中LTBP-1及TGF-βRⅡ的mRNA的錶達水平均低于對照組包皮組織(2-△△α2).免疫組化結果顯示:LTBP-1和TGF-βRⅡ的染色彊度較正常人包皮組織降低,差異有統計學意義(P<0.01). 結論 LTBP-1和TGF-βRⅡ的錶達下調,可導緻TCF-β活化及信號轉導通路的異常.
목적 탐토잠재결합단백(LTaP)-1급기Ⅱ형수체(TGF-βRⅡ)여첨예습우발병적상관성. 방법 채용실시형광정량PCR기술화SP면역조화기술분별검측30례CA피손급17례정상포피조직중LTBP화TGF-βRⅡ적mRNA화단백적표체. 결과 CA피손중LTBP-1급TGF-βRⅡ적mRNA적표체수평균저우대조조포피조직(2-△△α2).면역조화결과현시:LTBP-1화TGF-βRⅡ적염색강도교정상인포피조직강저,차이유통계학의의(P<0.01). 결론 LTBP-1화TGF-βRⅡ적표체하조,가도치TCF-β활화급신호전도통로적이상.
Objective To investigate the role of the expression of latent transforming growth factor beta binding protein-1 (LTBP-1) and transforming growth factor beta receptor type Ⅱ(TGF-beta R Ⅱ) in the pathogenesis of condyloma acuminatum (CA). Methods Samples were resected from the lesions of 30 patients with CA and prepuces of 17 normal human controls. The mRNA and protein expressions of LTBP-1 and TGF-betaR Ⅱ were assessed by quantitative real-time PCR and a streptavidin-biotin-peroxidase staining technique, respectively. Results As shown by Real time PCR, the mRNA expression levels of LTBP-1 and TGF-betaR Ⅱ were significantly higher in CA tissues than those in the controls, with the average value of 2 (-Delta Delta α) being 2.46 and 3.43, respectively. A lower intensity of stainning was observed for LTBP-1 and TGF-betaR Ⅱ in CA tissues compared with the normal controls (182.51±9.89 vs 167.78±12.56, 187.35± 11.23 vs 170.15±13.21, t = 5.62, 3.70 respectively, both P <0.01). Conclusion The decrease in the expres-sion of both LTBP-1 and TGF-betaR Ⅱ may lead to the abnormality in the activation of TGF-beta and signal transduction pathways.