Potent and selective partial ecdysone agonist activity of chromafenozide in Sf9 cells

被引:23
作者
Toya, T
Fukasawa, H
Masui, A
Endo, Y
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[2] Nippon Kayaku Co Ltd, Res & Dev Labs, Ageo, Saitama 3620064, Japan
关键词
chromafenozide; ANS-118; insect hormone; ecdysone; ponasterone A; luciferase; agonist; assay; Sf; 9; cells; Kc cells;
D O I
10.1006/bbrc.2002.6771
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
Chromafenozide (ANS-118) is a non-steroidal ecdysone mimic and its insecticidal effect is highly specific to lepidoptera. In order to evaluate the transcription-inducing activity via nuclear ecdysone receptor (EcR) and the mode of action of chromafenozide, ecdysone-responsive reporter gene assay systems were developed in Sf9 and Kc cells. Ponasterone A, a full EcR agonist, induced reporter transcription in a dose-dependent manner in both Sf9 and Kc cells. In contrast, chromafenozide activated reporter transcription with comparable potency to ponasterone A only in Sf9 cells, although its maximum activity was 4-fold lower than that of ponasterone A. When chromafenozide was applied together with ponasterone A to Sf9 cells, it antagonized ponasterone A at nanomolar concentrations. These results suggest that chromafenozide is a potent partial EcR agonist specific to lepidoptera; it appears to bind lepidopteran EcR with comparable affinity to ponasterone A, but may activate the EcR in a different manner. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:1087 / 1091
页数:5
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