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在定量体外模型中,肿瘤坏死因子-α、白细胞介素-6和白细胞介素-8不会促进人子宫内膜上皮细胞与间皮细胞的黏附。

Tumour necrosis factor-alpha, interleukin-6 and interleukin-8 do not promote adhesion of human endometrial epithelial cells to mesothelial cells in a quantitative in vitro model.

作者信息

Debrock Sophie, De Strooper Bart, Vander Perre Sarah, Hill Joseph A, D'Hooghe Thomas M

机构信息

Leuven University Fertility Center, UZ Gasthuisberg, KU Leuven, Belgium.

出版信息

Hum Reprod. 2006 Mar;21(3):605-9. doi: 10.1093/humrep/dei375. Epub 2005 Oct 27.

Abstract

BACKGROUND

A key factor in the pathogenesis of endometriosis is the endometrial-peritoneal adhesion. To study the pathogenesis of endometriosis, a quantitative in vitro assay (QIVA) was developed to measure in vitro adhesion between human endometrial epithelial cells and mesothelial cells using commercially available cell lines. Using the QIVA, the hypothesis was tested that tumour necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6) and interleukin-8 (IL-8) promote adhesion of endometrial epithelial cells to mesothelial cells.

METHODS

Mesothelial cells were pre-treated with TNF-alpha, IL-6 or IL-8 in various concentrations (ranging from 0 to 1000 IU/ml) for 24 h. Confluent endometrial epithelial cells were labelled with [35S]methionine, added to the confluent mesothelial cells and incubated for 1 h. After incubation, non-adhering cells were removed and adherent cells were solubilized and their [35S]methionine radioactivity was counted to quantify the adherence of endometrial epithelial cells to mesothelial cells.

RESULTS

The in vitro adhesion of human endometrial epithelial cells to human mesothelial cells was inhibited in a dose-dependent manner by TNF-alpha (P=0.0007), IL-6 (P<0.0001) and IL-8 (P=0.0004).

CONCLUSIONS

Using a quantitative in vitro adhesion assay, we were unable to confirm our hypothesis that TNF-alpha, IL-6 and IL-8 promote the in vitro adhesion between endometrial epithelial cells and mesothelial cells.

摘要

背景

子宫内膜异位症发病机制中的一个关键因素是子宫内膜-腹膜粘连。为了研究子宫内膜异位症的发病机制,开发了一种定量体外测定法(QIVA),以使用市售细胞系来测量人子宫内膜上皮细胞与间皮细胞之间的体外粘连。使用QIVA,检验了肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和白细胞介素-8(IL-8)促进子宫内膜上皮细胞与间皮细胞粘连的假说。

方法

将间皮细胞用不同浓度(0至1000 IU/ml)的TNF-α、IL-6或IL-8预处理24小时。将汇合的子宫内膜上皮细胞用[35S]甲硫氨酸标记,加入到汇合的间皮细胞中并孵育1小时。孵育后,去除未粘附的细胞,将粘附的细胞溶解,并对其[35S]甲硫氨酸放射性进行计数,以量化子宫内膜上皮细胞与间皮细胞的粘附。

结果

TNF-α(P = 0.0007)、IL-6(P < 0.0001)和IL-8(P = 0.0004)以剂量依赖性方式抑制人子宫内膜上皮细胞与人间皮细胞的体外粘连。

结论

使用定量体外粘连测定法,我们无法证实TNF-α、IL-6和IL-8促进子宫内膜上皮细胞与间皮细胞体外粘连的假说。

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