Mozhenok T, Belyaeva T, Bulychev A, Kuznetsova I, Leontieva E, Faddejeva M
Institute of Cytology, Russian Academy of Sciences, St Petersburg, Russia.
Cell Biol Int. 1998;22(6):465-72. doi: 10.1006/cbir.1998.0281.
Effects of biologically active compounds bilirubin (BR), farmorubicin (FR), and chelerythrine (CR) on phagosome-lysome (P-L) fusion in mouse peritoneal macrophages were studied using fluorescent dye acridine orange as lysosomal labelling and yeast cells as target. It was found that all three compounds tested enhanced P-L fusion. To investigate mechanisms of these effects, changes in fluidity of rat liver lysosomal membranes under influence of BR, FR and CR were studied by measuring fluorescence intensity, lifetime, and polarization of DPH or TMA-DPH incorporated in isolated rat liver lysosomes. In order to characterize the cytoskeleton changes under the action of these biologically active compounds F-actin content in peritoneal macrophages of mice was determined. Our results demonstrate that BR action induces a decrease in DPH and TMA-DPH polarization, FR increases DPH and TMA-DPH polarization, and CR causes only an increase in TMA-DPH polarization in lysosomal membranes. All three compounds tested increase F-actin content in peritoneal macrophages. Thus, the effect of BR on P-L fusion is connected with increasing fluidity of lysosomal membranes and the cytoskeleton changes. The enhancement of P-L fusion under the action of FR and CR can most likely be explained by changes of the cytoskeleton state.
以荧光染料吖啶橙作为溶酶体标记物,酵母细胞作为靶标,研究了生物活性化合物胆红素(BR)、法莫柔比星(FR)和白屈菜红碱(CR)对小鼠腹腔巨噬细胞吞噬体 - 溶酶体(P - L)融合的影响。结果发现,所测试的这三种化合物均增强了P - L融合。为了研究这些作用的机制,通过测量掺入分离的大鼠肝溶酶体中的DPH或TMA - DPH的荧光强度、寿命和偏振度,研究了BR、FR和CR对大鼠肝溶酶体膜流动性的影响。为了表征这些生物活性化合物作用下的细胞骨架变化,测定了小鼠腹腔巨噬细胞中的F - 肌动蛋白含量。我们的结果表明,BR的作用导致溶酶体膜中DPH和TMA - DPH偏振度降低,FR增加DPH和TMA - DPH偏振度,而CR仅导致溶酶体膜中TMA - DPH偏振度增加。所测试的这三种化合物均增加了腹腔巨噬细胞中的F - 肌动蛋白含量。因此,BR对P - L融合的影响与溶酶体膜流动性增加和细胞骨架变化有关。FR和CR作用下P - L融合的增强很可能可以用细胞骨架状态的变化来解释。