Department of Development Research, Pharmaceutical Research Center, Mochida Pharmaceutical Co., Ltd., Gotemba, Japan.
Fertil Steril. 2011 Dec;96(6):1485-1489.e4. doi: 10.1016/j.fertnstert.2011.09.040. Epub 2011 Oct 20.
To investigate the effect of dienogest on the expression of Toll-like receptor (TLR) 4 in human endometrial epithelial cells.
Prospective basic research study.
Pharmaceutical research center.
PATIENT(S): None.
INTERVENTION(S): Not applicable.
MAIN OUTCOME MEASURE(S): TLR4 in the immortalized progesterone receptor-expressing human endometrial epithelial cell line, EM-PR, was activated with lipopolysaccharide and high-mobility group box 1 (LPS/HMGB1) in the presence or absence of the synthetic progestin dienogest or endogenous progesterone. The production of interleukin (IL)-8, IL-6, and monocyte chemoattractant protein (MCP)-1 and the mRNA expression of TLR4 were measured with the use of ELISA and real-time reverse-transcription polymerase chain reaction respectively and nuclear factor (NF)-κB reporter gene assays were performed. The role of TLR4 was assayed with the use of TLR4-siRNA-transfected cells.
RESULT(S): Coadministration of LPS/HMGB1 induced the production of IL-8, IL-6, and MCP-1, TLR4 mRNA expression, and NF-κB activity in EM-PR cells, and dienogest inhibited all of these parameters. TLR4 knockdown using TLR4 siRNA reduced IL-8 production.
CONCLUSION(S): Dienogest inhibits TLR4 mRNA expression and subsequent IL-8 production induced by TLR4 agonists via an inhibitory effect on NF-κB activation in human endometrial epithelial cells. This pharmacologic effect of dienogest may contribute to its therapeutic effect on abnormal inflammation of endometrium.
研究地诺孕素对人子宫内膜上皮细胞 Toll 样受体 4(TLR4)表达的影响。
前瞻性基础研究。
药物研究中心。
无。
无。
用脂多糖和高迁移率族蛋白 B1(LPS/HMGB1)激活永生化孕激素受体表达的人子宫内膜上皮细胞系 EM-PR,观察在合成孕激素地诺孕素或内源性孕激素存在或不存在的情况下,TLR4 的激活情况。采用酶联免疫吸附试验和实时逆转录聚合酶链反应分别检测白细胞介素(IL)-8、IL-6 和单核细胞趋化蛋白(MCP)-1 的产生和 TLR4 的 mRNA 表达,并进行核因子κB 报告基因检测。采用 TLR4-siRNA 转染细胞检测 TLR4 的作用。
LPS/HMGB1 共处理诱导 EM-PR 细胞产生 IL-8、IL-6 和 MCP-1、TLR4 mRNA 表达和 NF-κB 活性,地诺孕素抑制所有这些参数。TLR4 siRNA 降低 TLR4 表达可减少 IL-8 的产生。
地诺孕素通过抑制 NF-κB 激活,抑制人子宫内膜上皮细胞 TLR4 激动剂诱导的 TLR4 mRNA 表达和随后的 IL-8 产生。地诺孕素的这种药理作用可能有助于其治疗子宫内膜异常炎症的作用。