Barkan R S, Alekseev V Iu
Tsitologiia. 1993;35(4):73-80.
The influence of cytochalasin B (CB) on the epidermal growth factor (EGF) intracellular degradation and release of low-molecular products of degradation into the culture medium were investigated using two cell lines, A431 and 3T3. Investigated parameters were registered 3.0-4.5 h after the beginning of 125I-EGF endocytosis at 37 degrees C. With A431 cells it was shown that actin cytoskeleton disorganization significantly reduced the rate of 125I-EGF final degradation: a high amount of 125I-EGF, still retained cell-associated, and a reduced amount of low-molecular degradation products were released into the medium in experiments with CB addition. That is in agreement with our previous results (Barkan et al., 1988), revealing a long-term accumulation of EGF-rhodamine fluorescence in a juxtanuclear area of A431 cells after CB treatment. Nevertheless when similar experiments were performed on Swiss 3T3 cells, previously used as a model for demonstrating the inhibitory effect of CB on DNA synthesis stimulation by EGF (Barkan, Nikol'skiĭ, 1986), we could not find such a distinct influence of CB on the process of degradation of internalised 125I-EGF.
利用A431和3T3两种细胞系,研究了细胞松弛素B(CB)对表皮生长因子(EGF)细胞内降解以及低分子降解产物释放到培养基中的影响。在37℃开始125I-EGF内吞作用3.0 - 4.5小时后记录研究参数。对于A431细胞,结果显示肌动蛋白细胞骨架紊乱显著降低了125I-EGF最终降解速率:在添加CB的实验中,大量仍与细胞相关的125I-EGF以及释放到培养基中的低分子降解产物数量减少。这与我们之前的结果(Barkan等人,1988年)一致,该结果表明CB处理后A431细胞近核区域中EGF-罗丹明荧光长期积累。然而,当对瑞士3T3细胞进行类似实验时(之前该细胞系被用作证明CB对EGF刺激DNA合成的抑制作用的模型,Barkan,Nikol'skiĭ,1986年),我们未发现CB对内化的125I-EGF降解过程有如此明显的影响。