检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:吴灏 吴欣帆 梁宇强[1] 蓝昭杨 赖玲芝 WU Hao;WU Xing-fan;LIANG Yu-qiang;LAN Zhao-yang;LAI Ling-zhi(Maoming People’s Hospital Emergency ICU,Maoming 525000,China;Maoming People’s Hospital Department of Stomatology,Maoming 525000,China)
机构地区:[1]茂名市人民医院急诊ICU,广东茂名525000 [2]茂名市人民医院口腔科,广东茂名525000
出 处:《广东医科大学学报》2024年第4期390-394,共5页Journal of Guangdong Medical University
基 金:茂名市科技计划项目(2022125)。
摘 要:目的探讨落新妇苷在体外促进血管生成过程中的影响。方法将体外培养的人脐静脉内皮细胞(HUVECs)中分别加入不同浓度(0、1、10、20、40μmol/L)的落新妇苷,通过MTT检测HUVECs的增殖能力;划痕实验检测细胞迁移能力;基质胶小管形成实验检测细胞管腔形成能力;Western blot检测血管内皮生长因子A(VEGFA)、血管内皮生长因子受体2(VEGFR-2)及血管性血友病因子(VWF)的蛋白表达情况。结果将不同浓度落新妇苷处理HUVECs 6、12和24 h后,细胞的增殖数目与对照组相比差异无统计学意义(P>0.05),而落新妇苷作用细胞48 h后,40μmol/L组细胞的增殖数与各组相比差异均有统计学意义(P<0.01或0.001)。划痕实验显示10μmol/L组6、12和24 h有大量的细胞向中间的划痕区域迁移,细胞分布广泛,较对照组显著增多(P<0.01);24 h时,10μmol/L组划痕愈合面明显多于1、20μmol/L组(P<0.01)。与对照组比较,10μmol/L组形成的管腔样结构最多,各浓度落新妇苷处理组形成的节点数、主节段长度及网格数均显著增加(P<0.05)。落新妇苷能显著增加VEGFA、VEGFR-2和VWF的蛋白表达,1、10μmol/L组较对照组明显增高(P<0.01)。结论落新妇苷可促进HUVECs细胞迁移及管腔形成。Objective The aim of this study is to investigate the effect of astilbin on angiogenesis in vitro.Methods Different concentrations(0,1,10,20,40μmol/L)of astilbin were added into HUVECs cultured in vitro,and the proliferation ability of HUVECs was detected by using MTT.The ability of cell migration was detected by scratch test,and the ability of cell lumen formation was determined by using matrix glue tubule formation test.The expression of angiogenesis-related factors(VEGFA,VEGFR-2,and VWF)was detected by using Western blot.Results There was no significant difference in the number of HUVECs in astilbin treatment with different concentrations compared with the control group(P>0.05),while the number of cells in the 40μmol/L group was statistically different from that of the control group after 48 h(P<0.01 or 0.001).The Scratch test showed that a large number of cells migrated to the middle scratch area in the 10μmol/L group at 6,12 and 24 h,with a wide distribution of cells,significantly increasing compared to the control group,and the difference was statistically significant(P<0.01).The migration of HUVECs in the 10μmol/L group was significantly increased compared to the 1μmol/L group and the 20μmol/L group at 24 h(P<0.05).Compared with the control group,the most lumen-like structures were formed in the 10μmol/L group,and the number of nodes,main segment length and mesh number were significantly increased in the astilbin treatment groups at all concentrations(P<0.05).Astilbin could significantly increase the expression of angiogenic factors VEGFA,VEGFR-2 and VWF,which were significantly higher in 1 and 10μmol/L groups than in the control group(P<0.01).Conclusion Astilbin can promote the migration and angiogenesis of HUVECs cells.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.7