皖南医学院学报
皖南醫學院學報
환남의학원학보
ACTA ACADEMIAE MEDICINAE WANNAN
2014年
2期
108-110
,共3页
17β-雌二醇%子宫组织%DLL1基因
17β-雌二醇%子宮組織%DLL1基因
17β-자이순%자궁조직%DLL1기인
17β-estrogen%uterine tissue%DLL1 gene
目的:研究高水平17β-雌二醇持续刺激去卵巢小鼠,对子宫组织DLL1基因表达的影响。方法:将16只小鼠随机平均分为正常对照组和去卵巢E2实验组(手术造模+E2干预);TRIzol一步法提取两组小鼠子宫组织总RNA,采用RT-PCR法扩增目的基因及内参基因的目的片段,紫外光下观察电泳结果并采用QuantityOne-4.6.2凝胶分析软件测定目标带光强度值。结果:两组小鼠子宫组织标本均出现目的基因DLL1与内参基因Gapdh的目标带,DLL1/Gapdh光强度的比值分别为0.33±0.12、0.78±0.11,两者差异有统计学意义(P<0.05),并且去卵巢E2实验组明显高于正常对照组。结论:高剂量E2的持续干预可显著提高去卵巢小鼠子宫组织DLL1基因的表达水平,可能是雌激素依赖性子宫组织细胞不正常增殖的病理基础。
目的:研究高水平17β-雌二醇持續刺激去卵巢小鼠,對子宮組織DLL1基因錶達的影響。方法:將16隻小鼠隨機平均分為正常對照組和去卵巢E2實驗組(手術造模+E2榦預);TRIzol一步法提取兩組小鼠子宮組織總RNA,採用RT-PCR法擴增目的基因及內參基因的目的片段,紫外光下觀察電泳結果併採用QuantityOne-4.6.2凝膠分析軟件測定目標帶光彊度值。結果:兩組小鼠子宮組織標本均齣現目的基因DLL1與內參基因Gapdh的目標帶,DLL1/Gapdh光彊度的比值分彆為0.33±0.12、0.78±0.11,兩者差異有統計學意義(P<0.05),併且去卵巢E2實驗組明顯高于正常對照組。結論:高劑量E2的持續榦預可顯著提高去卵巢小鼠子宮組織DLL1基因的錶達水平,可能是雌激素依賴性子宮組織細胞不正常增殖的病理基礎。
목적:연구고수평17β-자이순지속자격거란소소서,대자궁조직DLL1기인표체적영향。방법:장16지소서수궤평균분위정상대조조화거란소E2실험조(수술조모+E2간예);TRIzol일보법제취량조소서자궁조직총RNA,채용RT-PCR법확증목적기인급내삼기인적목적편단,자외광하관찰전영결과병채용QuantityOne-4.6.2응효분석연건측정목표대광강도치。결과:량조소서자궁조직표본균출현목적기인DLL1여내삼기인Gapdh적목표대,DLL1/Gapdh광강도적비치분별위0.33±0.12、0.78±0.11,량자차이유통계학의의(P<0.05),병차거란소E2실험조명현고우정상대조조。결론:고제량E2적지속간예가현저제고거란소소서자궁조직DLL1기인적표체수평,가능시자격소의뢰성자궁조직세포불정상증식적병리기출。
Objective:To examine the effects of constant high-dose 17β-estrogen stimulation on the Delta-like protein 1(DLL1) level in the uterine tissue of ovariectomized mice.Methods:Sixteen mice were randomly divided into normal control group and ovariectomized E2 experimental group (Model +E2 intervention).TRIzol reagent was used to extract the total RNA from the uterine tissues,and reverse transcription polymerase chain reaction(RT-PCR) was used to amplify the target sequences and internal control gene that were observed under UV light measured for the value of Adj .Vol with QuantityOne-4.6.2.Results:The target bands of gene DLL1 and Gapdh were detected in all samples,and the DLL1/Gapdh Adj.Vol.value of the two groups were 0.33 ±0.12,0.78 ±0.11,respectively.The two groups were statistically different(P <0.05),and the expression level was significantly higher in E2 group than the normal control group.Conclusion:Lasting high-dose estrogen stimulation could increase the gene DLL1expression in the uterine tissue of mice,which may explain the pathomechanism for abnormal growing of uterine tissue resulted from estrogen dependence .