Liu Li, Chen Li, Jiang Caixia, Guo Jing, Xie Yan, Kang Le, Cheng Zhongping
Department of Obstetrics and Gynecology, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, P.R. China.
Exp Ther Med. 2017 Dec;14(6):6125-6130. doi: 10.3892/etm.2017.5316. Epub 2017 Oct 16.
A previous study by our group has demonstrated that lipopolysaccharide (LPS) induces adenomyosis through stimulating inflammatory cell proliferation and invasive growth of stromal cells via Toll-like receptor 4 (TLR4) signaling. The present study aimed to investigate the effects of berberine (BBR) on LPS-induced ectopic endometrial stromal cells (EESCs) isolated from patients with adenomyosis. The viability of EESCs treated with LPS or LPS plus BBR was detected by a cell counting kit-8 assay, and the cell cycle distribution and apoptosis were evaluated by flow cytometry. The effect of BBR on the expression of key molecules of inflammatory proliferation and invasive growth of LPS-induced EESCs was also evaluated. BBR significantly inhibited the LPS-induced proliferation of EESCs in a dose- and time-dependent manner. BBR induced cell cycle arrest in G0/G1 phase and enhanced apoptosis of LPS-induced EESCs. Furthermore, BBR inhibited the expression of interleukin (IL)-6, IL-8, transforming growth factor-β, epithelial growth factor, vascular endothelial growth factor and matrix metalloproteinase 2 in LPS-induced EESCs. To the best of our knowledge, the present study was the first to demonstrate that BBR has a protective effect on ameliorating the LPS-induced progression of adenomyosis. This result may provide a novel therapeutic strategy for the clinical treatment of the disease.
我们团队之前的一项研究表明,脂多糖(LPS)通过Toll样受体4(TLR4)信号通路刺激炎性细胞增殖和基质细胞侵袭性生长,从而诱发子宫腺肌病。本研究旨在探讨黄连素(BBR)对从子宫腺肌病患者分离出的LPS诱导的异位子宫内膜基质细胞(EESCs)的影响。采用细胞计数试剂盒-8法检测用LPS或LPS加BBR处理的EESCs的活力,并通过流式细胞术评估细胞周期分布和细胞凋亡情况。还评估了BBR对LPS诱导的EESCs炎性增殖和侵袭性生长关键分子表达的影响。BBR以剂量和时间依赖性方式显著抑制LPS诱导的EESCs增殖。BBR诱导细胞周期停滞于G0/G1期,并增强LPS诱导的EESCs的凋亡。此外,BBR抑制LPS诱导的EESCs中白细胞介素(IL)-6、IL-8、转化生长因子-β、上皮生长因子、血管内皮生长因子和基质金属蛋白酶2的表达。据我们所知,本研究首次证明BBR对改善LPS诱导的子宫腺肌病进展具有保护作用。这一结果可能为该疾病的临床治疗提供一种新的治疗策略。