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:林海华[1,2] 晏维[1] 田德安[1] 黄焕军[1] 夏羽佳[1] 周珍珍[1] 涂炜[1] 邓欢[1] 廖家智[1]
机构地区:[1]华中科技大学同济医学院附属同济医院消化内科,武汉430030 [2]深圳市盐田区人民医院内科,深圳518081
出 处:《华中科技大学学报(医学版)》2011年第5期529-532,536,共5页Acta Medicinae Universitatis Scientiae et Technologiae Huazhong
基 金:国家自然科学基金资助项目(No.30973497)
摘 要:目的初步探讨神经生长因子Netrin-1对人肝癌细胞HepG2抗失巢凋亡的作用及相关机制。方法采用脂质体转染的方法,将Netrin-1的真核表达质粒转染到肝癌细胞HepG2中,Western blot检测Netrin-1的表达;用软琼脂集落试验、悬浮培养模型及流式细胞检测的方法观察肝癌细胞HepG2抗失巢凋亡的特性。结果肝癌细胞HepG2在失巢状态下可以聚集成团生长,并与贴壁生长有相似的凋亡比例。与对照组细胞相比,稳定转染Netrin-1真核质粒的HepG2细胞在软琼脂中形成细胞集落的数量明显增加,在悬浮培养模型中形成细胞团的直径更大,在失粘附状态下的细胞凋亡比例明显降低;磷脂酰肌醇3-激酶(PI3K)通路的抑制剂LY294002能增加转染细胞在失粘附状态下的凋亡比例。结论肝癌细胞HepG2具有抗失巢凋亡的特性,Netrin-1可以增强HepG2细胞抗失巢凋亡的能力,其机制可能与PI3-K通路相关。Objective Anoikis,which is a special form of programmed cell death,plays an important role in cell development,tissue homeostasis,disease pathogenesis,and tumor metastasis.In this study,we use hepatocellular carcinoma HepG2 cells to investigate the effects of the nerve growth factor Netrin-1 on anoikis. Methods Netrin-1 was stably transfected into HepG2 cells.The Netrin-1 expression level was detected by Western blot.The apoptosis of HepG2 cells was assayed by soft agar colony model and suspension culture model. Results The HepG2 cells in suspension culture model had the similar apoptosis ratio with the cells in attached culture model.Netrin-1 could increase the number of HepG2 cell colonies in soft agar colony model,increase the diameters of HepG2 cell colonies and decrease the apoptosis ratio of HepG2 cells in suspension culture model.PI3K inhibitor LY294002 could antagonize the reduced HepG2 cell apoptosis induced by Netrin-1. Conclusion The HepG2 cell is anoikis resistant.Netrin-1 can enhance the ability of anoikis resistance of HepG2 cells,which may be associated with the activation of PI3K.
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:216.73.216.3