中华消化外科杂志
中華消化外科雜誌
중화소화외과잡지
CHINESE JOURNAL OF DIGESTIVE SURGERY
2013年
1期
57-60
,共4页
高红%高飞%弭杰%伍美%张志波%王维林
高紅%高飛%弭傑%伍美%張誌波%王維林
고홍%고비%미걸%오미%장지파%왕유림
Hirschsprung病%Wnt10b%mRNA表达%蛋白表达
Hirschsprung病%Wnt10b%mRNA錶達%蛋白錶達
Hirschsprung병%Wnt10b%mRNA표체%단백표체
Hirschsprung disease%Wnt10b%mRNA expression%Protein expression
目的 分析Wnt10b基因在先天性巨结肠症(HD)中的表达,探讨其在HD发生中的意义.方法 收集2003年至2010年中国医科大学附属盛京医院经病理检查证实的散发性HD狭窄段和正常段组织标本各60例.采用HE染色和免疫组织化学染色方法检测标本中Wnt10b的表达情况;再用荧光实时定量PCR(qRT-PCR)、Western blot从其基因和蛋白水平检测HD中Wnt10b的表达情况,并对其表达进行定量与比较分析.数据采用独立样本t检验.结果 经HE染色检测,60例患儿HD诊断明确,标本符合本研究要求.Wnt10b在HD狭窄段肠壁的肌间和黏膜下细胞胞质内呈强阳性反应,而在HD正常段肠壁的肌间和黏膜下细胞胞质内表达呈弱阳性或阴性;经免疫组织化学染色检测Wnt10b在HD狭窄段蛋白阳性面积百分率为0.061%±0.014%,正常段为0.006%±0.005%,两者比较,差异有统计学意义(t=2.955,P<0.05).经qRT-PCR检测,Wnt10b在HD狭窄段肠管中mRNA相对含量为23.5±1.6,高于正常段肠管中的13.1±1.7(t=1.687,P<0.05);60例患儿的HD狭窄段肠管组织标本中Wnt10b mRNA高表达者45例,低表达者15例.经Western blot检测,Wnt10b在HD狭窄段肠管中蛋白相对表达量为35.2±2.3,高于正常段肠管中的19.1±1.3(t =2.046,P<0.05);60例患儿的HD狭窄段肠管组织标本中Wnt10b蛋白高表达者43例,低表达者17例.结论 Wnt10b mRNA与蛋白在HD肠管组织中的异常表达,与HD的发生有密切关系,可能在先天性消化道畸形的肠道发育中起一定作用.
目的 分析Wnt10b基因在先天性巨結腸癥(HD)中的錶達,探討其在HD髮生中的意義.方法 收集2003年至2010年中國醫科大學附屬盛京醫院經病理檢查證實的散髮性HD狹窄段和正常段組織標本各60例.採用HE染色和免疫組織化學染色方法檢測標本中Wnt10b的錶達情況;再用熒光實時定量PCR(qRT-PCR)、Western blot從其基因和蛋白水平檢測HD中Wnt10b的錶達情況,併對其錶達進行定量與比較分析.數據採用獨立樣本t檢驗.結果 經HE染色檢測,60例患兒HD診斷明確,標本符閤本研究要求.Wnt10b在HD狹窄段腸壁的肌間和黏膜下細胞胞質內呈彊暘性反應,而在HD正常段腸壁的肌間和黏膜下細胞胞質內錶達呈弱暘性或陰性;經免疫組織化學染色檢測Wnt10b在HD狹窄段蛋白暘性麵積百分率為0.061%±0.014%,正常段為0.006%±0.005%,兩者比較,差異有統計學意義(t=2.955,P<0.05).經qRT-PCR檢測,Wnt10b在HD狹窄段腸管中mRNA相對含量為23.5±1.6,高于正常段腸管中的13.1±1.7(t=1.687,P<0.05);60例患兒的HD狹窄段腸管組織標本中Wnt10b mRNA高錶達者45例,低錶達者15例.經Western blot檢測,Wnt10b在HD狹窄段腸管中蛋白相對錶達量為35.2±2.3,高于正常段腸管中的19.1±1.3(t =2.046,P<0.05);60例患兒的HD狹窄段腸管組織標本中Wnt10b蛋白高錶達者43例,低錶達者17例.結論 Wnt10b mRNA與蛋白在HD腸管組織中的異常錶達,與HD的髮生有密切關繫,可能在先天性消化道畸形的腸道髮育中起一定作用.
목적 분석Wnt10b기인재선천성거결장증(HD)중적표체,탐토기재HD발생중적의의.방법 수집2003년지2010년중국의과대학부속성경의원경병리검사증실적산발성HD협착단화정상단조직표본각60례.채용HE염색화면역조직화학염색방법검측표본중Wnt10b적표체정황;재용형광실시정량PCR(qRT-PCR)、Western blot종기기인화단백수평검측HD중Wnt10b적표체정황,병대기표체진행정량여비교분석.수거채용독립양본t검험.결과 경HE염색검측,60례환인HD진단명학,표본부합본연구요구.Wnt10b재HD협착단장벽적기간화점막하세포포질내정강양성반응,이재HD정상단장벽적기간화점막하세포포질내표체정약양성혹음성;경면역조직화학염색검측Wnt10b재HD협착단단백양성면적백분솔위0.061%±0.014%,정상단위0.006%±0.005%,량자비교,차이유통계학의의(t=2.955,P<0.05).경qRT-PCR검측,Wnt10b재HD협착단장관중mRNA상대함량위23.5±1.6,고우정상단장관중적13.1±1.7(t=1.687,P<0.05);60례환인적HD협착단장관조직표본중Wnt10b mRNA고표체자45례,저표체자15례.경Western blot검측,Wnt10b재HD협착단장관중단백상대표체량위35.2±2.3,고우정상단장관중적19.1±1.3(t =2.046,P<0.05);60례환인적HD협착단장관조직표본중Wnt10b단백고표체자43례,저표체자17례.결론 Wnt10b mRNA여단백재HD장관조직중적이상표체,여HD적발생유밀절관계,가능재선천성소화도기형적장도발육중기일정작용.
Objective To study the expression and clinical significance of Wnt10b gene in tissue samples of Hirschsprung disease (HD).Methods Sixty samples of stenotic intestines and 60 samples of normal intestines were collected from 60 patients with sporadic HD who were admitted to the Shengjing Hospital of China Medical University from 2003 to 2010.Tissue samples were stained by hematoxylin and eosin (HE),and then the expression of Wnt10b gene in the tissues was detected by immunohistochemical staining.The mRNA and protein expressions of Wnt10b in HD were detected by quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot.All data were analyzed by two independent sample t test.Results The results of HE staining confirmed HD in the 60 patients,and the samples met the requirement of the study.The expressions of Wnt10b were strong positive in the plasma of intramuscular and submucosal cells in stenotic intestines,while weak positive or negative in normal intestines.The results of immunohistochemical staining showed that the percentages of positive proteins in the stenotic intestines and the normal intestines were 0.061% ± 0.014% and 0.006% ± 0.005%,respectively,with a significant difference (t =2.955,P < 0.05).The results of qRT-PCR showed that the relative quantification of mRNA of Wnt10b was 23.5 ± 1.6 in the stenotic intestines,which was significantly higher than 13.1 ± 1.7 in the normal intestines (t =1.687,P <0.05).High mRNA expressions of Wnt10b were observed in 45 patients with HD,and low mRNA expressions of Wnt10b were observed in 15 patients.The results of Western blot showed that the relative protein expression of Wnt10b was 35.2 ± 2.3 in the stenotic intestines,which was significantly higher than 19.1 ± 1.3 in the normal intestines (t =2.046,P < 0.05).High protein expressions of Wnt10b were observed in 43 patients,and low protein expressions of Wnt10b were observed in 17 patients.Conclusion There is a close relationship between the abnormal mRNA and protein expressions of Wnt10b in the intestines,which might play a role in the pathogensis congenital malformation of the alimentary tract.