人脐带间充质干细胞培养上清对米非司酮处理的人子宫内膜基质细胞存活、凋亡和子宫内膜容受性的影响  

Effect of culture supernatant of human umbilical cord mesenchymal stem cells on survival,apoptosis and endometrium receptivity of human endometrial stromal cells after treated with mifepristone

作　　者：武梦雪 陈士玲 刘艳 米旭光 林秀英[1] 付建华[1] 方艳秋[1] WU Mengxue;CHEN Shiing;LIU Yan;MI Xuguang;LIN Xiuying;FU Jianhua;FANG Yanqiu(Center of Peproductive Medicine,People’s Hospital,Jilin Province,Changchun 130021,China)

机构地区：[1]吉林省人民医院生殖医学中心,吉林长春130021

出　　处：《吉林大学学报（医学版）》2024年第1期79-87,共9页Journal of Jilin University：Medicine Edition

基　　金：吉林省科技厅科技发展计划项目(20200801019GH,YDZJ202102CXJD076,20200403081SF,20230204036YY,20230203051SF);吉林省卫健委卫生健康技术创新项目(2020J106,2020J108,2021lc059,2021lc061)。

摘　　要：目的:探讨人脐带间充质干细胞培养上清(hUCMSCs-Sup)对米非司酮(Ms)处理的人子宫内膜基质细胞(hEndoSCs)增殖、凋亡和子宫内膜容受性的影响,并阐明其可能的作用机制。方法:体外培养hEndoSCs,分为对照组和40、60、80及100μmol·L-1 Ms组,MTT法检测各组细胞存活率。hEndoSCs分为对照组、40μmol·L-1 Ms组和60μmol·L-1 Ms组,流式细胞术检测各组细胞凋亡率,Western blotting法检测各组细胞中凋亡相关蛋白B细胞淋巴瘤2 (Bcl-2)和Bcl-2相关X蛋白(Bax)蛋白表达水平并计算Bcl-2/Bax比值。hUCMSCs-Sup作用后,hEndoSCs分为对照组、Ms组、Ms+hUCMSCs-Sup组和Ms+hUCMSCs-Sup+3-甲基腺嘌呤(3-MA)组,MTT法检测各组细胞存活率,流式细胞术检测各组细胞凋亡率,Western blotting法检测各组细胞中微管相关蛋白1轻链3B-Ⅱ(LC3B-Ⅱ)和微管相关蛋白1轻链3B-Ⅰ(LC3B-Ⅰ)蛋白表达水平并计算LC3B-Ⅱ/LC3B-Ⅰ比值,实时荧光定量PCR (RT-qPCR)法检测各组细胞中子宫内膜容受性标志分子mRNA表达水平。结果:与对照组比较,40、60、80和100μmol·L-1 Ms组细胞存活率明显降低(P<0.05),且具有时间和剂量依赖性。与对照组比较,40和60μmol·L-1 Ms组细胞凋亡率明显升高(P<0.05),细胞中Bcl-2/Bax比值明显降低(P<0.05)。hUCMSCs-Sup作用后,与对照组比较,Ms组细胞存活率和细胞中LC3B-Ⅱ/LC3B-Ⅰ比值明显降低(P<0.05),细胞凋亡率明显升高(P<0.05),细胞中同源框基因A10 (HOXA10)、白血病抑制因子(LIF)和整合素亚基β3 (ITGB3) mRNA表达水平明显降低(P<0.05);与Ms组比较,Ms+hUCMSCs-Sup组细胞存活率和细胞中LC3B-Ⅱ/LC3B-Ⅰ比值明显升高(P<0.05),细胞凋亡率明显降低(P<0.05),细胞中HOXA10、LIF和ITGb3 mRNA表达水平表达明显升高(P<0.05);与Ms+hUCMSCs-Sup组比较,Ms+hUCMSCs-Sup+3-MA组细胞存活率和细胞中LC3B-Ⅱ/LC3B-Ⅰ比值明显降低(P<0.05)。结论:hUCMSCs-Sup可提高Ms处理后hEndoSCs的存活率,降低其凋亡率,提高子宫内膜容�Objective:To discuss the effect of human umbilical cord mesenchymal stem cells culture supernatant(hUCMSCs-Sup)on the proliferation,apoptosis,and endometrium receptivity of the human endometrial stromal cells(hEndoSCs)treated with mifepristone(Ms),and to clarify the possible mechanism.Methods:The hEndoSCs were cultured in vitro and divided into control group and 40,60,80,and 100μmol·L-1 Ms groups.The survival rates of the cells in various groups were detected by MTT assay.The hEndoSCs were divided into control group,40μmol·L-1 Ms group,and 60μmol·L-1 Ms group.The apoptotic rates of the cells in various groups were detected by flow cytometry;the expression levels of apoptosis-related protein B-cell lymphoma-2(Bcl-2)and Bcl-2-associated X protein(Bax)proteins in the cells in various groups were detected by Western blotting method,and the ratio of Bcl-2/Bax was calculated.After treated with hUCMSCs-Sup,the hEndoSCs were divided into control group,Ms group,Ms+hUCMSCs-Sup group,and Ms+hUCMSCs-Sup+3-methyladenine(3-MA)group.The survival rates of the cells in various groups were detected by MTT assay;the apoptotic rates of the cells in various groups were detected by flow cytometry;the expression levels of microtubule-associated protein 1 light chain 3B-Ⅱ(LC3B-Ⅱ)and microtubule-associated protein 1 light chain 3B-I(LC3B-Ⅰ)proteins in the cells in various groups were detected by Western blotting method,and the ratio of LC3B-Ⅱ/LC3B-Ⅰwas calculated;the expression levels of endometrium receptivity marker molecules mRNA in the cells in various groups were detected by real-time fluorescence quantitative PCR(RT-qPCR)method.Results:Compared with control group,the survival rates of the cells in 40,60,80,and 100μmol·L-1 Ms groups were significantly decreased(P<0.05)in a time-dependent and dose-dependent manner.Compared with control group,the apoptotic rates of the cells in 40 and 60μmol·L-1 Ms groups were significantly increased(P<0.05),and the ratios of Bcl-2/Bax were significantly decreased(P<0.05).After tre

关 键 词：脐带间充质干细胞 人子宫内膜基质细胞 细胞凋亡 细胞自噬 子宫内膜容受性 

分 类 号：R711[医药卫生—妇产科学]