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苏云金芽孢杆菌δ-内毒素和蜂毒素对昆虫细胞腺苷酸环化酶的激活作用。毒性与环磷酸腺苷无关。

Activation of insect cell adenylate cyclase by Bacillus thuringiensis delta-endotoxins and melittin. Toxicity is independent of cyclic AMP.

作者信息

Knowles B H, Farndale R W

机构信息

Department of Biochemistry, University of Cambridge, U.K.

出版信息

Biochem J. 1988 Jul 1;253(1):235-41. doi: 10.1042/bj2530235.

Abstract

Insecticidal Bacillus thuringiensis (Bt) delta-endotoxins are cytolytic to a range of insect cell lines in vitro. Addition of Bt var. aizawai or var. israelensis toxins to Mamestra brassicae (cabbage moth) cells in vitro increased intracellular cyclic AMP, which was paralleled by activation of adenylate cyclase in isolated membranes. Var. kurstaki toxin, which does not lyse M. brassicae cells, had no effect on cyclic AMP concentrations in intact cells, but was able to stimulate adenylate cyclase in membrane preparations. In contrast, the bee-venom toxin melittin, which is also cytolytic, increased intracellular cyclic AMP in whole cells, but inhibited adenylate cyclase in isolated membranes. Octopamine and forskolin also increased cyclic AMP in cells, but were not cytolytic. When added to cells at concentrations exceeding their LC90 (concentration causing 90% cell death), melittin and var. israelensis toxins caused cell lysis without a concomitant increase in intracellular cyclic AMP. Taken together, these results suggest that activation of adenylate cyclase by cytolytic toxins is a secondary effect (related perhaps to interactions of these toxins with membrane lipids) and is neither necessary nor sufficient for cytolysis.

摘要

苏云金芽孢杆菌(Bt)的杀虫δ-内毒素在体外对一系列昆虫细胞系具有细胞溶解作用。在体外将Bt变种aizawai或变种israelensis毒素添加到甘蓝夜蛾细胞中会增加细胞内的环磷酸腺苷(cAMP),这与分离膜中腺苷酸环化酶的激活同时发生。不裂解甘蓝夜蛾细胞的变种kurstaki毒素对完整细胞中的cAMP浓度没有影响,但能够刺激膜制剂中的腺苷酸环化酶。相比之下,同样具有细胞溶解作用的蜂毒毒素蜂毒肽会增加全细胞内的cAMP,但会抑制分离膜中的腺苷酸环化酶。章鱼胺和福斯高林也会增加细胞中的cAMP,但没有细胞溶解作用。当以超过其LC90(导致90%细胞死亡的浓度)的浓度添加到细胞中时,蜂毒肽和变种israelensis毒素会导致细胞裂解,而细胞内的cAMP不会随之增加。综上所述,这些结果表明,细胞溶解毒素对腺苷酸环化酶的激活是一种次要效应(可能与这些毒素与膜脂的相互作用有关),对于细胞溶解既不是必需的也不是充分的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d969/1149280/5cb1efff9f2e/biochemj00228-0239-a.jpg

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