Addition of G418 and other aminoglycoside antibiotics to mammalian cells results in the release of GPI-anchored proteins

被引:12
作者
Kung, M [1 ]
Stadelmann, B [1 ]
Brodbeck, U [1 ]
Butikofer, P [1 ]
机构
[1] UNIV BERN,INST BIOCHEM & MOL BIOL,CH-3012 BERN,SWITZERLAND
关键词
G418 (geneticin); alkaline phosphatase; glycosylphosphatidylinositol; transfection; COS-1; cell; human erythrocyte;
D O I
10.1016/S0014-5793(97)00452-3
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
Resistance to the neomycin analogue G418 forms the basis of a dominant marker selection system for mammalian cells transfected with the bacterial neomycin gene. We found that COS-1 cells stably transfected with the neomycin resistance gene had a greater than 50% reduction in cell-associated glycosylphosphatidylinositol (GPI)-anchored alkaline phosphatase (AP). A similarly reduced amount of AP was also observed in wild-type COS-1 cells incubated in the presence of G418 or other aminoglycoside antibiotics. The AP was released from cells into the culture supernatant in its GPI-anchored form, Our data suggest that the G418-induced reduction of AP involves a vesiculation process of COS-1 cells. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:333 / 338
页数:6
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