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机构地区:[1]华中科技大学同济医学院附属同济医院妇产科,武汉430030
出 处:《中国优生与遗传杂志》2008年第2期34-36,共3页Chinese Journal of Birth Health & Heredity
摘 要:目的检测胎儿生长受限(FGR)患者胎盘组织中血管生成素-2(angiopoietin-2,Ang-2)的表达水平,并探讨其与FGR的关系。方法采用免疫组织化学方法(SP法)和逆转录聚合酶链反应(RT-PCR)检测FGR组和对照组的胎盘组织中Ang-2表达的定位和表达量的差异。结果1.S-P:(1)Ang-2在胎盘的绒毛滋养细胞、血管内皮细胞及血管周围细胞均有表达。(2)FGR组Ang-2的平均光密度较正常对照组显著下降(P<0.05)。2.RT-PCR:FGR组Ang-2 mRNA的表达量下降,于正常对照组相比有明显意义(P<0.05)。结论妊娠晚期Ang-2水平显著下降可能是FGR发病机制中的一个重要因素。Objective: To detect the expression of angiopoietin -2 (Ang -2) in placentas, and to evaluate the role of Ang -2 in FGR. Methods: Immunohistochemistry (SP) was used to investigate the distribution and location of angiopoietin -2 and the semi - quantitative method of reverse transcription polymerase chain reaction ( RT - PCR) was employed to investigate the mRNA expression levels of angiopoietin- 2 in placenta tissues of normal pregnant women and women with FGR. Results: 1. S- P: (1) Ang- 2 was located in trophoblast, endothelial cells and paravascular cells of placentas. (2) The mean density of angiopoietin -2 in group of FGR was significantly lower than that in normal group ( P 〈0. 05). 2. RT - PCR: Compared with the normal group, the mRNA expression levels of angiopoietin -2 was reduced ( P 〈0.05). Conclusion: The expression of Ang -2 was greatly reduced in late pregnancy, It maybe play an important role in the pathogenic causes of preeclampsia.
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