[x射线和奎宁(Atebrin)或氯喹(Resochin)单独或联合对单层培养的哈丁-帕西黑色素瘤细胞影响的超微结构研究]。

Strahlentherapie Pub Date : 1985-11-01
R Pfab, D O Schachtschabel, H F Kern
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引用次数: 0

摘要

在指数生长阶段,以4gy或8gy的x射线剂量照射哈丁-帕西黑色素瘤(HPM 73细胞)的单层细胞,4天后未见任何超微结构变化,而8 Gy照射的细胞则出现轻微损伤,如线粒体和液泡肿胀。电镜显示,单独添加亚致死量(6 × 10(-6) M)的奎宁(阿特布林)或氯喹(雷索钦)不会导致显著的细胞修饰。用8 Gy预照射后,用6 × 10(-6) M的阿特布林(atbrin)或6 × 10(-6) M的氯喹(Resochin)孵育4天,黑色素瘤细胞出现严重损伤。细胞质中液泡和分离结构增加。线粒体增多肿胀,细胞表面微绒毛减少。然而,微管和微丝似乎更明显。在此处理下,黑色素浓度升高。细胞核体积增大,似乎没有染色质。细胞对阿特布林(atbrin)和氯喹(Resochin)的这些反应可以用已知的这些物质对DNA合成的抑制作用来解释,特别是在DNA修复过程中。微管-微丝系统的变化可能与细胞内消化过程的增加有关,这些过程与辐射损伤结构的分解代谢有关。
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[Ultrastructural studies of the effect of x-rays and quinacrine (Atebrin) or chloroquine (Resochin)--alone or in combination--on Harding-Passey melanoma cells in monolayer culture].

Monolayer cells of a Harding-Passey melanoma (HPM 73 cells) which were irradiated during the phase of exponential growth with an X-ray dose of 4 Gy of 8 Gy did not show any ultrastructural changes four days after 4 Gy, whereas cells irradiated with 8 Gy showed slight damages such as swollen mitochondria and vacuoles. As shown by the electron microscope, a sole addition of a sublethal quantity (6 X 10(-6) M) of quinacrine (Atebrin) or chloroquine (Resochin) did not lead to significant cell modifications. Those melanoma cells with were pre-irradiated with 8 Gy and then incubated during four days with 6 X 10(-6) M of quinacrine (Atebrin) or 6 X 10(-6) M of chloroquine (Resochin) showed severe damages. There was an increased rate of vacuoles and segregational structures in cytoplasm. The mitochondria were increased and swollen and the cellular surfaces had less microvilli. However, microtubules and microfilaments seemed more distinct. The melanin concentration increased under this treatment. The cell nuclei were increased in volume and seemed to be rather void of chromatin. These reactions of cells on quinacrine (Atebrin) and chloroquine (Resochin) are explained by the known inhibition effect exerted by these substances on DNA synthesis, especially as far as the processes of DNA reparation are concerned. The changes of the microtubule-microfilament system could be due to a correlation with the increase of digestive intracellular processes connected with the catabolism of radiation-damaged structures.

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