Lan Q, Gerenday A, Fallon A M
Department of Entomology, University of Minnesota, St. Paul 55108.
In Vitro Cell Dev Biol Anim. 1993 Oct;29A(10):813-8. doi: 10.1007/BF02634349.
To provide a framework for biochemical investigation of ecdysteroid action in Aedes albopictus mosquito cells, we examined the effect of 20-hydroxyecdysone on cell growth and morphology, synthesis of inducible proteins (EIPs), and expression of a transfected gene regulated by a synthetic ecdysteroid response element. When cells were cultured in the continuous presence of 10(-6) M 20-hydroxyecdysone, the rate of growth decreased and subtle changes in cell morphology were observed. In both Aedes aegypti and A. albopictus cells, synthesis of a small number of radiolabeled proteins, which appeared as minor bands on sodium dodecyl sulfate-polyacrylamide gels, was induced by treatment with 20-hydroxyecdysone. On two-dimensional polyacrylamide gels, 11 EIPs, ranging in size from approximately 22 to 52 kDa, were identified in A. albopictus C7-10 cells. Ten inducible proteins were localized in the cytoplasmic fraction; EIP28 and EIP31 were detected in both cytoplasmic and nuclear extracts, and EIP29 was detected only in the nucleus, at a very low level. None of these proteins corresponded to small heat shock proteins, whose genes are 20-hydroxyecdysone-inducible in some Drosophila cell lines. The juvenile hormone analog, methoprene, induced expression of a 25 kDa protein in C7-10 cells. Although 20-hydroxyecdysone sustained the synthesis of this methoprene-inducible protein, synthesis did not occur in the presence of 20-hydroxyecdysone alone. In transfected A. albopictus cells, expression of a recombinant DNA construct containing two tandem synthetic ecdysteroid regulatory elements based on a D. melanogaster small heat shock protein gene was modestly induced by 20-hydroxyecdysone.
为了提供一个在白纹伊蚊细胞中进行蜕皮甾酮作用生化研究的框架,我们检测了20-羟基蜕皮酮对细胞生长和形态、诱导蛋白(EIPs)合成以及由合成蜕皮甾酮反应元件调控的转染基因表达的影响。当细胞在10(-6) M 20-羟基蜕皮酮持续存在的情况下培养时,生长速率下降,并且观察到细胞形态有细微变化。在埃及伊蚊和白纹伊蚊细胞中,用20-羟基蜕皮酮处理可诱导合成少量放射性标记蛋白,这些蛋白在十二烷基硫酸钠-聚丙烯酰胺凝胶上呈现为次要条带。在二维聚丙烯酰胺凝胶上,在白纹伊蚊C7-10细胞中鉴定出11种EIPs,大小约为22至52 kDa。10种诱导蛋白定位于细胞质部分;EIP28和EIP31在细胞质和核提取物中均被检测到,而EIP29仅在细胞核中以非常低的水平被检测到。这些蛋白均与小热休克蛋白不对应,小热休克蛋白的基因在一些果蝇细胞系中是20-羟基蜕皮酮可诱导的。保幼激素类似物烯虫酯在C7-10细胞中诱导了一种25 kDa蛋白的表达。虽然20-羟基蜕皮酮维持了这种烯虫酯诱导蛋白的合成,但单独存在20-羟基蜕皮酮时不会发生合成。在转染的白纹伊蚊细胞中,基于黑腹果蝇小热休克蛋白基因的含有两个串联合成蜕皮甾酮调控元件的重组DNA构建体的表达受到20-羟基蜕皮酮的适度诱导。