Zhang Yuan, Zhao Nannan, Zhao Haijun, Cui Yugui, Liu Jiayin
Center of Clinical Reproductive Medicine, First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Center of Clinical Reproductive Medicine, First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China. Email:
Zhonghua Fu Chan Ke Za Zhi. 2014 Feb;49(2):125-9.
To study the expression of tight junction factors in human placental tissues derived from assisted reproductive technology (ART) and natural pregnancy and its role in placental barrier.
Ten placental samples were collected from the women who had undergone ART treatment and 11 placenta were collected from control group. Transmission electron microscope (TEM) examination was utilized to detect the morphology of placental tight junctions. The mRNA of claudin (CLDN) 1, CLDN4, CLDN5, CLDN8, zonula occudens (ZO) 1 was detected by real-time PCR and the protein of CLDN4, CLDN8 and occludin (OCLN) were measured by western blot.
TEM microscopy results showed that placenta samples derived both ART and control placenta had normal microscopic histological features of tight junctions, localized in the apical part of the syncytium and also between the cell-cell contacts of fetal blood vessel endothelial. The expression level of CLDN4 mRNA were 0.87 ± 0.17 in ART group and 1.18 ± 0.30 in control group, respectively. The expression level of CLDN8 mRNA were 3.25 ± 2.32 in ART group and 1.08 ± 0.41 in control group, respectively. The mRNA level of CLDN4 and CLDN8 were significantly differentially expressed in ART derived placenta when compared with control groups. The expression level of CLDN1, CLDN5, OCLN and ZO1 mRNA were 0.49 ± 0.44, 0.80 ± 0.20, 0.92 ± 0.18 in ART group and 1.09 ± 0.82, 1.21 ± 0.78, 0.80 ± 0.27 in control group, respectively, in which there were no significant differences between two groups. Western Blot analysis showed the protein levels of tight junctions CLDN4, CLDN8 and OCLN did not differ between groups.
Tight junction factors were expressed in human placental tissues. Tight junction derived from ATR platenta might have mild dysfunction.
研究紧密连接因子在辅助生殖技术(ART)和自然妊娠来源的人胎盘组织中的表达及其在胎盘屏障中的作用。
收集10例接受ART治疗的女性的胎盘样本,对照组收集11例胎盘。采用透射电子显微镜(TEM)检查来检测胎盘紧密连接的形态。通过实时PCR检测闭合蛋白(CLDN)1、CLDN4、CLDN5、CLDN8、闭合小带(ZO)1的mRNA,通过蛋白质印迹法检测CLDN4、CLDN8和闭合蛋白(OCLN)的蛋白质。
TEM显微镜检查结果显示,ART组和对照组胎盘样本均具有紧密连接的正常微观组织学特征,位于合体滋养层顶端以及胎儿血管内皮细胞间接触处。ART组CLDN4 mRNA表达水平分别为0.87±0.17,对照组为1.18±0.30。ART组CLDN8 mRNA表达水平分别为3.25±2.32,对照组为1.08±0.41。与对照组相比,ART来源的胎盘组织中CLDN4和CLDN8的mRNA水平存在显著差异表达。ART组CLDN1、CLDN5、OCLN和ZO1 mRNA表达水平分别为0.49±0.44、0.80±0.20、0.92±0.18,对照组分别为1.09±0.82、1.21±0.78、0.80±0.27,两组间无显著差异。蛋白质印迹分析显示,紧密连接CLDN4、CLDN8和OCLN的蛋白质水平在两组间无差异。
紧密连接因子在人胎盘组织中表达。ART胎盘来源的紧密连接可能存在轻度功能障碍。