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作 者:刘子瑶 黄玥 王超[1] 李涛[1] 王晶哲 蔺博涵 王子璇 孙晓春[1] 陈华标 LIU Ziyao;HUANG Yue;WANG Chao;LI Tao;WANG Jingzhe;LIN Bohan;WANG Zixuan;SUN Xiaochun;CHEN Huabiao(School of Medicine,Jiangsu University,Zhenjiang Jiangsu 212013;Laboratory of Marshall International Diagnosis and Treatment Center for Digestive Tract Diseases,Shanghai Dongfang Hospital,Shanghai 200120,China;Vaccine&Immunotherapy Center,Massachusetts General Hospital,Harvard Medical School,Boston Massachusetts 02114,USA)
机构地区:[1]江苏大学医学院,江苏镇江212013 [2]上海市东方医院马歇尔消化道疾病国际诊疗中心实验室,上海200120 [3]哈佛医学院麻省总医院疫苗和免疫治疗中心,马萨诸塞州波士顿02114
出 处:《江苏大学学报(医学版)》2022年第1期44-49,共6页Journal of Jiangsu University:Medicine Edition
基 金:江苏大学科研项目(8421280005)。
摘 要:目的:构建尼古丁诱导的小鼠生精细胞体外损伤模型,探讨小鼠骨髓间质干细胞来源的胞外囊泡(mouse bone marrow mesenchymal stem cell-derived extracellular vesicles,mBMMSCs-EVs)对于小鼠GC-1生精细胞损伤的修复作用。方法:采用不同浓度尼古丁(0、8、16、32μg/mL)处理GC-1生精细胞24、48、72 h,通过MTT实验筛选尼古丁诱导GC-1生精细胞损伤的最适浓度和时间;将GC-1生精细胞分为对照组、尼古丁组、尼古丁+胞外囊泡组;通过MTT实验、Transwell实验和流式细胞术凋亡实验观察mBMMSCs-EVs干预前后受损生精细胞GC-1生物学特性的变化。结果:MTT实验结果表明,32μg/mL尼古丁作用GC-1生精细胞24 h时,细胞增殖能力明显降低(P<0.05),mBMMSCs-EVs作用于尼古丁预处理后,细胞增殖能力明显增高(P<0.05);与对照组相比,尼古丁组GC-1生精细胞迁移能力明显降低,细胞凋亡能力明显升高(P均<0.01),与尼古丁组相比,尼古丁+胞外囊泡组生精细胞增殖和迁移能力明显升高,细胞凋亡能力明显下降(P<0.01或<0.05)。结论:mBMMSCs-EVs可以逆转尼古丁引发的GC-1生精细胞增殖、迁移能力的损伤以及细胞凋亡。Objective:To construct an in vitro model of nicotine-induced injury of mouse spermatogenic cells and to explore the repairing effect of mouse bone marrow mesenchymal stem cell-derived extracellular vesicles(mBMMSCs-EVs)on the nicotine-induced damage of spermatogenic cells GC-1.Methods:Different concentrations(0,8,16,32μg/mL)of nicotine were used to treat spermatogenic cell GC-1 for 24,48,72 h,respectively;and the optimal concentration of nicotine and time of treatment to induce damage on GC-1 cells were screened by MTT assay.The spermatogenic cells GC-1 were divided into control group,nicotine group and nicotine+extracellular vesicle group.MTT,Transwell and apoptosis experiments were used to evaluate the changes in the biological characteristics of damaged GC-1 cell before and after the intervention of mBMMSCs-EVs.Results:The results of MTT assay showed that the proliferation of GC-1 was significantly decreased when the concentration of nicotine was 32μg/mL for 24 h(P<0.05),mBMMSCs-EVS increased cell proliferation after treatment with nicotine(P<0.05);compared with the control group,GC-1 cells in nicotine group showed significantly reduced migration and increased apoptosis(P<0.01);compared with the nicotine group,nicotine+extracellular vesicle group showed significantly increased cell proliferation and migration,and decreased the apoptotic ability(P<0.05 or<0.01).Conclusion:mBMMSCs-EVs may repair the damage of nicotine on the proliferation and migration of spermatogenic cells and inhibited nicotine-induced apoptosis of spermatogenic cells.
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