Lack of gradual regulation of tetracycline-controlled gene expression by the tetracyclin-repressor VP16 transactivator (tTA) in cultured cells

被引:8
作者
Hop, C
deWaard, V
vanMourik, JA
Pannekoek, H
机构
[1] UNIV AMSTERDAM,ACAD MED CTR,DEPT BIOCHEM,NL-1105 AZ AMSTERDAM,NETHERLANDS
[2] NETHERLANDS RED CROSS,BLOOD TRANSFUS SERV,CENT LAB,DEPT BLOOD COAGULAT,AMSTERDAM,NETHERLANDS
关键词
tetracycline; transactivator tTA; von Willebrand factor; MDCK-II cell; VONWILLEBRAND-FACTOR; MAMMALIAN-CELLS; TRANSGENIC MICE;
D O I
10.1016/S0014-5793(97)00179-8
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
Von Willebrand factor (vWF) is an essential multimeric protein for adhesion of platelets to an injured vessel wall. Endothelial cells secrete vWF by either a constitutive or a regulated pathway. It is unknown whether the secretory partitioning of vWF is dependent on the level of VWF synthesis. We employed the widely applied tetracycline-controlled transactivator system (tTA) to study the regulation of vWF mRNA synthesis in stably transfected Madin Darby kidney (MDCK-II) cells in a quantitative manner. Immunofluorescence staining with anti-vWF antibodies revealed that increasing the concentration of tetracycline resulted in a decreased number of MDCK-II cells that synthesize vWF. Apparently, tTA-regulated gene expression in an individual cell functions as an 'on/off' system rather than regulating the level of gene expression in a dose-response manner, as reported previously. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:167 / 171
页数:5
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