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作 者:顾华芬[1] 衣欢 陈亚萍[1] 赵海红[1] 张丽文[1]
机构地区:[1]复旦大学附属上海市第五人民医院,上海200240 [2]福建省妇幼保健院,福建福州350000
出 处:《实用妇产科杂志》2017年第7期516-520,共5页Journal of Practical Obstetrics and Gynecology
基 金:上海市卫生计划生育委员会课题(编号:20134213)
摘 要:目的:通过研究常见的邻苯二甲酸酯类中邻苯二甲酸二(2-乙基己)酯(DEHP)对人滋养细胞HTR-8/SVneo(简称HTR-8)功能的影响及机制,初步探讨DEHP导致稽留流产的机制。方法:采用不同浓度DEHP溶液干预HTR-8细胞,CCK-8检测细胞毒性、流式细胞仪检测细胞凋亡及细胞周期的变化。用Western-blot方法探讨DEHP对凋亡相关蛋白的影响,分析DEHP致凋亡的可能通路。结果:(1)CCK-8检测细胞毒性示:DEHP≥30 ng/ml作用24小时及48小时,HTR-8细胞活性明显受抑制(P<0.05);DEHP浓度为20 ng/ml时作用24小时,对HTR-8细胞活性无明显抑制作用;但作用48小时,HTR-8细胞活性同样受到抑制(P<0.01)。(2)凋亡实验结果:小剂量DEHP(15 ng/ml)能抑制HTR-8细胞凋亡(P<0.05);而大剂量DEHP(30 ng/ml)促进细胞凋亡(P<0.05)。(3)流式细胞检测发现:DEHP浓度15 ng/ml作用HTR-8细胞24小时,细胞阻滞于S期(P<0.05);DEHP浓度30 ng/ml作用HTR-8细胞24小时,细胞阻滞于G0/G1期(P<0.01)。(4)DEHP浓度15 ng/ml作用HTR-8细胞6小时,促凋亡因子Bax蛋白表达下降而凋亡抑制因子Bcl-2的蛋白表达增加。结论:大剂量DEHP(≥30 ng/ml)使滋养细胞活力明显受抑制,且不受作用时间的影响。小剂量DEHP(≤15 ng/ml)对滋养细胞活力无明显影响,但抑制其凋亡,可能与小剂量的DEHP下调Bax、上调Bcl-2的表达有关,这可能是DEHP致稽留流产的机制之一。Objective:To explore the probable effect of DEHP(one of most common phthalate esters)on the function of human trophoblastic cell line HTR-8/SVneo(HTR-8) and discuss the mechanisms of DEHP leading to missed abortion. Methods. To observe changes in cell toxicity with different concentrations of DEHP by CCK-8,and detect apoptosis and cell cycle by flow cytometry. To investigate the effect of DEHP on apoptosis associated protein by Western-blot method,and the possible pathway of DEHP inducing apoptosis. Results① CCK-8 assay for cytotoxicity showed that HTR-8 cells activity was significantly inhibited( P 〈 0.05)by DEHP ≥ 30 ng/ml for 24 h and 48 h and 20 ng/ml for48 h,while the activity of HTR-8 cells was not inhibited(P〉0.05) by 20 ng/ml for 24 h. ②Cell apoptosis: small dose of DEHP(15 ng/ml)inhibited the apoptosis of HTR-8 cells ( P 〈 0.05), while large dose of DEH P ( 30 ng/ml) promoted cell apoptosis ( P 〈 0.05 ). ③ FCM results showed that HTR-8 cell cycle arrested in S phase( P〈0.05)by 15 ng/ml of DEHP for24 hand stayed in G0/G1 phase (P〈0.01)by 30 ng/ml of DEHP for 24 h. ④Decreased expression of Bax(apoptosis inducer)and increased expression of Bcl-2 (apoptosis inhibitor)were observed in HTR-8 cells with 15ng/ml DEHP for 6 h. Conclu- sions.Large dose of DEHP (≥ 30 ng/ml)inhibits activity of trophoblast significantly with no effect from time. Small dose of DEHP(15 ng/ml)has no obvious effect on trophoblast cell viability, but inhibits the apoptosis of cell. Down-regulation of Bax and up-regulation of Bcl-2 by small dose of DEHP may be one of the mechanisms of missed abortion induced by DEHP.
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