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New NCI-N87-derived human gastric epithelial line after human telomerase catalytic subunit over-expression 被引量:1
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作者 Kathy Saraiva-Pava Nazanin Navabi +3 位作者 Emma C Skoog Sara K Lindén Mónica Oleastro Mónica Roxo-Rosa 《World Journal of Gastroenterology》 SCIE CAS 2015年第21期6526-6542,共17页
AIM:To establish a cellular model correctly mimicking the gastric epithelium to overcome the limitation in the study of Helicobacter pylori(H.pylori) infection.METHODS:Aiming to overcome this limitation,clones of the ... AIM:To establish a cellular model correctly mimicking the gastric epithelium to overcome the limitation in the study of Helicobacter pylori(H.pylori) infection.METHODS:Aiming to overcome this limitation,clones of the heterogenic cancer-derived NCI-N87 cell line were isolated,by stably-transducing it with the human telomerase reverse-transcriptase(h TERT) catalytic subunit gene.The clones were first characterized regarding their cell growth pattern and phenotype.For that we measured the clones' adherence properties,expression of cell-cell junctions' markers(ZO-1 and E-cadherin) and ability to generate a sustained transepithelial electrical resistance.The gastric properties of the clones,concerning expression of mucins,zymogens and glycan contents,were then evaluated by haematoxylin and eosin staining,Periodic acid Schiff(PAS) and PAS/Alcian Blue-staining,immunocytochemistry and Western blot.In addition,we assessed the usefulness of the h TERT-expressing gastric cell line for H.pylori research,by performing co-culture assays and measuring the IL-8 secretion,by ELISA,upon infection with two H.pylori strains differing in virulence.RESULTS:Compared with the parental cell line,themost promising NCI-hT ERT-derived clones(CL5 and CL6) were composed of cells with homogenous phenotype,presented higher relative telomerase activities,better adhesion properties,ability to be maintained in culture for longer periods after confluency,and were more efficient in PAS-reactive mucins secretion.Both clones were shown to produce high amounts of MUC1,MUC2 and MUC13.NCI-hT ERT-CL5 mucins were shown to be decorated with blood group H type 2(BG-H),Lewis-x(Lex),Ley and Lea and,in a less extent,with BG-A antigens,but the former two antigens were not detected in the NCI-h TERT-CL6.None of the clones exhibited detectable levels of MUC6 nor sialylated Lex and Lea glycans.Entailing good gastric properties,both NCIhT ERT-clones were found to produce pepsinogen-5 and human gastric lipase.The progenitor-like phenotype of NCI-hT ERT-CL6 cells was highlighted by large nuclei and by the apical vesicular-like distribution of mucin 5AC and Pg5,supporting the accumulation of mucus-secreting and zymogens-chief mature cells functions.CONCLUSION:These traits,in addition to resistance to microaerobic conditions and good responsiveness to H.pylori co-culture,in a strain virulence-dependent manner,make the NCI-hT ERT-CL6 a promising model for future in vitro studies. 展开更多
关键词 Helicobacter pylori infection Pathogenesis HUMAN gastric EPITHELIUM cellular model nci-n87cells
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转化生长因子β诱导肿瘤微环境改变促进胃癌NCI-N87细胞上皮间充质转化 被引量:4
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作者 徐群芳 谈文龙 赵锐 《国际药学研究杂志》 CAS CSCD 2014年第6期686-692,共7页
目的探讨微环境因子在转化生长因子β(TGF-β)诱导胃癌上皮-间充质转化(EMT)中的作用。方法建立了TGF-β诱导胃癌细胞发生EMT模型,利用实时定量PCR、免疫荧光染色技术检测了EMT相关指标的表达情况,采用Transwell迁移实验、侵袭实验、划... 目的探讨微环境因子在转化生长因子β(TGF-β)诱导胃癌上皮-间充质转化(EMT)中的作用。方法建立了TGF-β诱导胃癌细胞发生EMT模型,利用实时定量PCR、免疫荧光染色技术检测了EMT相关指标的表达情况,采用Transwell迁移实验、侵袭实验、划痕修复实验检测了胃癌细胞的转移能力;同时,利用实时定量PCR(RT-q PCR)和ELISA检测了TGF-β诱导刺激后胃癌微环境因子的改变,并通过免疫印迹检测了其下游信号分子的活性。结果 TGF-β能诱导胃癌细胞NCI-N87发生EMT改变,促进癌细胞迁移和侵袭。进一步研究发现,TGF-β能诱导表皮生长因子(EGF)和血管内皮生长因子(VEGF)表达上调,Dickkopf-1(DKK1)和分泌型卷曲受体蛋白1(SFRP1)表达降低,进而分别诱导PI3K/AKT和Wnt/β-连环蛋白(catenin)通路的激活。结论 TGF-β通过诱导胃癌微环境因子的改变促进胃癌NCI-N87细胞发生EMT。 展开更多
关键词 转化生长因子Β 胃癌 nci-n87细胞 上皮-间充质转化 肿瘤微环境 transforming growth factor β
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靶向HER2的抑制胃癌细胞功能性单抗的制备和鉴定 被引量:1
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作者 孙立新 冉宇靓 +4 位作者 胡海 遇珑 周转 赵西路 杨治华 《中国肿瘤生物治疗杂志》 CAS CSCD 2008年第1期14-19,共6页
目的:制备可特异识别人表皮生长因子受体-2(human epidermal growth factor receptor-2,HER2)膜抗原的单克隆抗体,筛选出亲和力较高并对胃癌细胞有明显抑制作用的克隆。方法:以高表达HER2膜抗原的人胃癌细胞系NCI-N87免疫BABL/c小鼠,免... 目的:制备可特异识别人表皮生长因子受体-2(human epidermal growth factor receptor-2,HER2)膜抗原的单克隆抗体,筛选出亲和力较高并对胃癌细胞有明显抑制作用的克隆。方法:以高表达HER2膜抗原的人胃癌细胞系NCI-N87免疫BABL/c小鼠,免疫小鼠脾细胞与小鼠骨髓瘤细胞SP2/0融合,ELISA法筛选出HER2反应阳性克隆株,活细胞免疫荧光法检测获得膜阳性克隆株,使用抗体亚型鉴定试剂盒鉴定抗体亚型,MTT法检测抗体对NCI-N87细胞增殖的抑制,采用与群司珠单抗的夹心ELISA和竞争抑制ELISA鉴定单抗结合HER2抗原的表位,免疫组化、Westernblotting进一步检测抗HER2抗体在不同条件下与HER2抗原反应情况。结果:细胞融合产生1442个单个集落的杂交瘤,重组HER2抗原ELISA筛选出HER2反应阳性克隆79株,活细胞免疫荧光检测获得较强膜阳性克隆7株,并测定其亚型,其中命名为15C15的1株属IgG1κ类单抗,免疫竞争及结合实验显示15C15与群司珠人源化抗体识别不同的表位。细胞增殖筛选显示15C15能显著抑制人胃癌NCI-N87细胞的增殖,在80μg/ml时抑制率可达34.8%。免疫组化显示15C15能识别部分石蜡包埋的HER2抗原,Westernblotting显示15C15不能结合电泳条件下变性为线形结构的HER2抗原。结论:建立了高通量制备、筛选和鉴定靶向HER2抑制胃癌细胞生长的功能性单抗技术,获得1株可特异识别HER2抗原的明显抑制胃癌细胞增殖的IgG1类单抗15C15,具有人源化改造后用于治疗的应用潜力。 展开更多
关键词 胃癌 NCI N87细胞系 人表皮生长因子受体-2 单克隆抗体
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