Suppr超能文献

Fas介导的细胞凋亡参与了利用缺失E1/E3的腺病毒载体对基因转导肝细胞的清除过程。

Fas-mediated apoptosis is involved in the elimination of gene-transduced hepatocytes with E1/E3-deleted adenoviral vectors.

作者信息

Okuyama T, Li X K, Funeshima N, Fujino M, Sasaki K, Kita Y, Kosuga M, Takahashi M, Saito H, Suzuki S, Yamada M

机构信息

Department of Genetics, National Children's Medical Research Center, Tokyo, Japan.

出版信息

J Gastroenterol Hepatol. 1998 Sep;13 Suppl:S113-8.

PMID:9792044
Abstract

Gene-transduced hepatocytes with E1/E3-deleted adenoviral vectors are eliminated immediately and the expression of transduced genes disappears rapidly following the vector administration. In this report, we analysed the involvement of apoptotic cell death in the elimination of hepatocytes infected with adenoviral vectors. An E1/E3-deleted adenoviral vector expressing Escherichia coli beta-galactosidase (LacZ) was injected via the portal vein into congenitally Fas-deficient mice (lpr), Fas ligand-deficient mice (gld) and their control mice, MRL and C3H. 5-Bromo-4-chloro-3-indolyl-beta-D-galactoside (X-gal) staining of the liver specimens showed that 80-100% of hepatocytes were LacZ positive at 7 days after virus administration, suggesting that most of the hepatocytes received the injected adenoviral vectors. In normal mice, the number of LacZ-positive cells decreased dramatically at 14 and 21 days after transduction and few positive cells were observed at day 28. Beta-galactosidase activity, quantified by the O-nitrophenyl-beta-D-galactopyranoside assay, gave comparable results to X-gal staining. At days 14 or 21, many apoptotic hepatocytes and apoptotic infiltrating cells were detected with the terminal deoxyribonucleotidyl transferase-mediated dUTP-digoxigenin nick end-labelling (TUNEL) in situ apoptosis detection method. This observation suggested that the apoptotic process was associated with the elimination of adenovirus-infected hepatocytes. To test the involvement of the Fas-Fas ligand interaction in this apoptotic process, the period of transgene expression was measured in lpr and gld mice, which had received the same amount of AxCALacZ. X-Gal histochemical analysis detected many LacZ-positive cells in lpr or gld mice liver even at 21 or 28 days after AxCALacZ injection. There were significant differences in the reduction rates of beta-galactosidase activity of liver homogenates between lpr and MRL, or gld and C3H mice. Based on these observations, we conclude that the Fas-mediated apoptotic process is involved in the elimination of hepatocytes infected with E1/E3-deleted adenoviral vectors.

摘要

携带E1/E3缺失腺病毒载体的基因转导肝细胞在载体给药后会立即被清除,转导基因的表达也会迅速消失。在本报告中,我们分析了凋亡性细胞死亡在清除感染腺病毒载体的肝细胞过程中的作用。将表达大肠杆菌β-半乳糖苷酶(LacZ)的E1/E3缺失腺病毒载体经门静脉注射到先天性Fas缺陷小鼠(lpr)、Fas配体缺陷小鼠(gld)及其对照小鼠MRL和C3H中。肝脏标本的5-溴-4-氯-3-吲哚基-β-D-半乳糖苷(X-gal)染色显示,在病毒给药后7天,80%-100%的肝细胞LacZ呈阳性,这表明大多数肝细胞接受了注射的腺病毒载体。在正常小鼠中,转导后14天和21天,LacZ阳性细胞数量急剧减少,在第28天时几乎观察不到阳性细胞。通过邻硝基苯-β-D-半乳糖苷检测法定量的β-半乳糖苷酶活性,得到了与X-gal染色相当的结果。在第14天或21天,采用末端脱氧核苷酸转移酶介导的dUTP-地高辛缺口末端标记(TUNEL)原位凋亡检测方法,检测到许多凋亡的肝细胞和凋亡浸润细胞。这一观察结果表明,凋亡过程与腺病毒感染肝细胞的清除有关。为了测试Fas-Fas配体相互作用在这一凋亡过程中的作用,在接受相同剂量AxCALacZ的lpr和gld小鼠中测量了转基因表达的持续时间。X-Gal组织化学分析在AxCALacZ注射后21天或28天,在lpr或gld小鼠肝脏中仍检测到许多LacZ阳性细胞。lpr与MRL,或gld与C3H小鼠肝脏匀浆中β-半乳糖苷酶活性的降低率存在显著差异。基于这些观察结果,我们得出结论,Fas介导的凋亡过程参与了清除感染E1/E3缺失腺病毒载体的肝细胞。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验