Jahanbin K Hodakaram, Ghafourian Mehri, Rashno Mohammad
Department of Immunology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Department of Immunology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran. Electronic Address:
Int J Fertil Steril. 2020 Jul;14(2):116-121. doi: 10.22074/ijfs.2020.6058. Epub 2020 Jul 15.
Several studies have shown that leukemia inhibitory factor (LIF) is one of the most important cytokines participating in the process of embryo implantation and pregnancy, while, the role of this factor on vascular endothelial factor-A (VEGF-A), as one of the most important angiogenic factor, has not been fully investigated yet. The aim of this study was to evaluate the effect of LIF on gene expression of in the choriocarcinoma cells (JEG-3).
In this experimental study, JEG-3 choriocarcinoma cells were treated with different concentrations of LIF (1, 10, and 50 ng) for 6, 12, 24, 48 and 72 hours. Expression of VEGF was analyzed by real-time PCR. Delta CTs were subjected to one-way analysis of variance (ANOVA) and a post hoc Tukey's test by SPSS version 25.0 software for data analyzing.
In the stimulated cells, different concentrations of LIF caused significant decrease of gene expression (P<0.05) at 12, 24 and 48 hours. In contrast, it was increased after 72 hours (P<0.001). Analysis of data after 6 hours also showed that level of gene expression was significantly decreased by increasing LIF concentration (P<0.001).
Expression level of gene was decreased in trophoblast cells (except after 72 hours) under the effect of different concentrations of LIF in a time-dependent manner. So, this study showed that further studies are needed to determine the effect of LIF on other angiogenic factors in trophoblast cells.
多项研究表明,白血病抑制因子(LIF)是参与胚胎着床和妊娠过程的最重要细胞因子之一,然而,该因子对作为最重要血管生成因子之一的血管内皮生长因子-A(VEGF-A)的作用尚未得到充分研究。本研究旨在评估LIF对绒毛膜癌细胞(JEG-3)中VEGF基因表达的影响。
在本实验研究中,用不同浓度的LIF(1、10和50纳克)处理JEG-3绒毛膜癌细胞6、12、24、48和72小时。通过实时PCR分析VEGF的表达。使用SPSS 25.0软件对ΔCT值进行单因素方差分析(ANOVA)和事后Tukey检验以进行数据分析。
在受刺激的细胞中,不同浓度的LIF在12、24和48小时导致VEGF基因表达显著降低(P<0.05)。相比之下,72小时后表达增加(P<0.001)。6小时后的数据分析还表明,随着LIF浓度增加,VEGF基因表达水平显著降低(P<0.001)。
在不同浓度LIF作用下,滋养层细胞中VEGF基因表达水平(72小时后除外)呈时间依赖性降低。因此,本研究表明需要进一步研究以确定LIF对滋养层细胞中其他血管生成因子的影响。