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

机译:光动力疗法在体内相互作用过程中激活的癌肉瘤细胞和腹膜巨噬细胞的精细结构

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Abstract: 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.' !32
机译:摘要:研究了宿主的光动力疗法激活的巨噬细胞(PDT-AM0)与大鼠Walker-256癌肉瘤靶细胞(腹水形式)的相互作用。腹膜巨噬细胞用不同浓度的Photofrin II(0.1到12 $mu@g/2.5乘以10 $ + 6 $ /细胞)敏化,并以He-Ne激光(632.8 nm; 10 mW)在不同剂量注量下辐照。 1.5至15 kJ / m $ + 2 $ /。通过以下参数估算PDT对巨噬细胞的激活程度:(1)体外测定细胞毒性和抑制细胞生长的活性,以及​​(2)在电子显微镜下观察。获得的结果表明:(1)在以0.8 mg敏化并暴露于He-Ne激光照射(3.0)的Photofrin II中,发现对Walker-256(39.7%)和K562(21.6%)细胞的细胞毒活性最高。 kJ / m $ + 2 $ /):(2)与正常巨噬细胞(NM0)相比,PDT-AM0对鼠Walker-256的抑制细胞活性较高(54.7%),对人K562细胞的抑制细胞活性较低(28.1%)。 ; (3)PDT-AM0在腹腔中的相互作用过程中,肿瘤细胞伴随着核和细胞质精细结构的强烈变化。综上所述,PDT在光活化巨噬细胞中的某些功能活性(细胞毒性,抑制细胞生长和吞噬作用)得到增强,并通过“体内”相互作用在Walker-256腹水癌肉瘤细胞中诱导超微结构改变。 !32

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