Zackroff Robert V, Hufnagel Linda A
Massachusetts College of Pharmacy and Health Sciences, School of Arts and Sciences, 179 Longwood Avenue, Boston, MA 02115 USA.
J Eukaryot Microbiol. 2002 Nov-Dec;49(6):475-7. doi: 10.1111/j.1550-7408.2002.tb00231.x.
Both cytochalasin D and latrunculin B reversibly inhibited Tetrahymena phagocytosis at concentrations similar to those effective in mammalian systems, even though ciliate actins are known to be highly divergent from mammalian actins. Overnight exposure to relatively low (0.25 microM) concentrations of latrunculin B induced resistance in Tetrahymena to the inhibitory effects of that drug, as well as cross-resistance to cytochalasin D. However, much higher (> 30 microM) concentrations of cytochalasin D were required for induction of cross-resistance to latrunculin B. Anti-actin drug resistance in Tetrahymena may involve a general multidrug resistance mechanism and/or specific feedback regulation of F-actin assembly and stability.
尽管已知纤毛虫肌动蛋白与哺乳动物肌动蛋白高度不同,但细胞松弛素D和拉特肌动蛋白B在与哺乳动物系统中有效浓度相似的情况下,均可可逆地抑制四膜虫的吞噬作用。过夜暴露于相对较低(0.25微摩尔)浓度的拉特肌动蛋白B会诱导四膜虫对该药物的抑制作用产生抗性,以及对细胞松弛素D的交叉抗性。然而,诱导对拉特肌动蛋白B的交叉抗性则需要高得多(>30微摩尔)的细胞松弛素D浓度。四膜虫中的抗肌动蛋白药物抗性可能涉及一般的多药抗性机制和/或F-肌动蛋白组装与稳定性的特定反馈调节。