Increased susceptibility to apoptosis of human hepatocarcinoma cells transfected with antisense N-acetylglucosaminyltransferase V cDNA

被引:27
|
作者
Guo, HB [1 ]
Liu, F [1 ]
Chen, HL [1 ]
机构
[1] Shanghai Med Univ, Dept Biochem, Minist Hlth, Key Lab Glycoconjugate Res, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
human hepatocarcinoma cell line; apoptosis; N-acetylglucosaminyltransferase V (GnT-V); antisense; all-trans-retinoic acid;
D O I
10.1006/bbrc.1999.1303
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The antisense cDNA of N-acetylglucosaminyltransferase V (GnT-V, EC 2.4.1.155) was constructed as pcDNA3/GnT-V-AS plasmid and transfected into 7721 cells, a human hepatocarcinoma cell line. The transfection was confirmed with Northern blot. By using HPLC and HRP-lectin staining, it was found that the cells transfected with pcDNA3/GnT-V-AS (GnT-V-AS/7721) expressed less GnT-V activity and beta-1,6-GlcNAc branching in the cell glycoproteins compared with the cells mock-transfected with the vector pcDNA3 (pcDNA3/7721). The growth rate of GnT-V-AS/7721 was decreased in serum-containing medium, while the cell death was accelerated in serum-free medium. The GnT-V-AS/7721 cells were more susceptible to the apoptosis induced by ATRA than the mock-transfected cells. This was evidenced by the obvious appearance of a hypoploid sub-G, fraction in the DNA histogram using FCM analysis, the more condensed new moon-type nuclei under morphological observation, and the more intensive TUNEL reaction for assaying the fragmented DNA. At the same time as GnT-V down-regulation by GnT-V-AS, an increase of another N-aceylglusaminyltransferase, GnT-III (EC 2.4.1.144), was observed, and the biological significance of this finding was discussed, (C) 1999 Academic Press.
引用
收藏
页码:509 / 517
页数:9
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