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Fine structure of carcinosarcoma cells and peritoneal macrophages activated by photodynamic therapy during their interaction in vivo

机译:在体内相互作用期间光动力治疗激活癌细胞细胞和腹膜巨噬细胞的细结构

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The interaction of the photodynamic therapy activated macrophages (PDT-AM0) of the host and rat Walker-256 carcinosarcoma target cells (ascitic form) was investigated. The periotoneal macrophages were sensitized with different concentrations of Photofrin II (0.1 to 12 $mu@g/2.5 multiplied by 10$+6$/ cells) and irradiated with He-Ne laser (632.8 nm; 10 mW) at different dose fluences varying between 1.5 and 15 kJ/m$+2$/. The degree of macrophage activation by PDT was estimated by means of the following parameters: (1) in vitro assay of cytotoxic and cytostatic activities and (2) observation at the electron microscopy. The results obtained indicate the following: (1) the highest rate of cytotoxic activity against Walker-256 (39.7%) and K562 (21.6%) cells was found in Photofrin II sensitized with 0.8 mg and exposure to He-Ne laser irradiation (3.0 kJ/m$+2$/): (2) the cytostatic activity of PDT-AM0 was higher against murine Walker-256 (54.7%) and lower on human K562 (28.1%) cells, in comparison with normal macrophages (NM0); (3) during interaction of PDT-AM0 in peritoneal cavity, the tumor cells were accompanied by strong changes in nuclear and cytoplasmic fine structure. Summing up, in photobioactivated macrophages by PDT some functional activities (cytotoxic, cytostatic and phagocytosis) were enhanced and induced ultrastructural changes in Walker-256 ascites carcinosarcoma cells by their interaction 'in vivo.'
机译:研究了光动力治疗活化巨噬细胞(PDT-AM0)的相互作用,对宿主和大鼠步行者-256癌靶细胞(腹水形式)进行了研究。蠕动巨噬细胞用不同浓度的Photofrin II(0.1至12 $ Mu@g / 2.5乘以10 $ + 6 $ /细胞),并在不同剂量流量不同的He-Ne激光(632.8nm; 10 mw)辐照1.5至15 kJ / m $ + 2 $ /。通过以下参数估计PDT的巨噬细胞活化程度:(1)在电子显微镜下的细胞毒性和细胞毒性活性的体外测定和(2)观察。得到的结果表明以下:(1)在光氯丁II中发现对步行者-256(39.7%)和K562(21.6%)细胞的最高细胞毒性活性速率在用0.8mg和He-Ne激光照射(3.0)中敏化KJ / M $ + 2 $ /):(2)与正常巨噬细胞(NM0)相比,PDT-AM0的细胞抑制活性较高,鼠窜梭-256(54.7%),低于人K562(28.1%)细胞。 ; (3)在PDT-AM0在腹膜腔中的相互作用过程中,肿瘤细胞伴有核和细胞质细结构的强烈变化。总结,在PDT的PDT中,一些功能性活性(细胞毒性,细胞毒性和吞噬作用)被提高,并通过它们的相互作用“在体内”的腹水 - 256腹水癌细胞的超微结构变化。

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