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子宫内膜异位症上皮细胞通过 NFkappaB 依赖途径诱导子宫内膜基质细胞中 MMPs 的表达。

Endometriotic epithelial cells induce MMPs expression in endometrial stromal cells via an NFkappaB-dependent pathway.

机构信息

Department of Obstetrics and Gynecology, Provincial Hospital Affiliated to Shandong University, Shandong, People's Republic of China.

出版信息

Gynecol Endocrinol. 2010 Jun;26(6):456-67. doi: 10.3109/09513590903366988.

Abstract

OBJECTIVE

To explore the stroma-epithelium interactions in endometriosis and to identify the possible signalling pathways involved in this cross-talk.

DESIGN

Laboratory study via primary cultured endometrial stromal and epithelial cells.

SETTING

University Hospital.

PATIENTS

Fifteen patients with endometriosis confirmed by histopathology were recruited in the study, and 12 women free of endometriosis were used as control group.

INTERVENTION(S): Specific NFkappaB inhibitor 1-Pyrrolidinecarbodithioic acid ammonium salt (PDTC) was used in cell cultures.

MAIN OUTCOME MEASURE(S): The expression and secretion of MMP-2, MMP-9, TIMP-1, TIMP-2 and the DNA-binding activity of NFkappaB in normal endometrial stromal cells or in co-cultures with normal or endometriotic epithelial cells from patients with endometriosis.

RESULT(S): Endometrial epithelial cells induced MMP-9 and MMP-2 expression in normal stromal cells in vitro. In co-cultures with endometriotic epithelial cells, normal endometrial stromal cells expressed and secreted higher MMP-2 (p < 0.05) and MMP-9 (p < 0.05). Specific inhibition of NFkappaB pathway in stromal cells abolished this induction effect by epithelial cells.

CONCLUSION(S): Endometriotic epithelial cells induce MMPs expression and secretion in normal endometrial stromal cells via an NFkappaB-dependent pathway in vitro. This cross-talk between epithelial cells and stromal cells may facilitate the implantation and extension of the ectopic foci and favour the development of the disease.

摘要

目的

探索子宫内膜异位症中的基质-上皮相互作用,并确定这种细胞间通讯中涉及的可能信号通路。

设计

通过原代培养的子宫内膜基质和上皮细胞进行实验室研究。

地点

大学医院。

患者

本研究纳入了 15 例经组织病理学证实的子宫内膜异位症患者,同时纳入了 12 例无子宫内膜异位症的女性作为对照组。

干预措施

在细胞培养中使用特定的 NFκB 抑制剂 1-吡咯烷二硫代氨基甲酸盐(PDTC)。

主要观察指标

正常子宫内膜基质细胞或与子宫内膜异位症患者正常或异位上皮细胞共培养中 MMP-2、MMP-9、TIMP-1、TIMP-2 的表达和分泌,以及 NFκB 的 DNA 结合活性。

结果

子宫内膜上皮细胞在体外诱导正常基质细胞中 MMP-9 和 MMP-2 的表达。与子宫内膜异位症上皮细胞共培养时,正常子宫内膜基质细胞表达和分泌更高水平的 MMP-2(p<0.05)和 MMP-9(p<0.05)。基质细胞中 NFκB 通路的特异性抑制消除了上皮细胞的这种诱导作用。

结论

子宫内膜异位症上皮细胞通过体外 NFκB 依赖性途径诱导正常子宫内膜基质细胞中 MMPs 的表达和分泌。上皮细胞和基质细胞之间的这种细胞间通讯可能有助于异位病灶的植入和扩展,并有利于疾病的发展。

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