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Mechanisms in photodynamic therapy: photosensitizers and cellular localization on K562 cells

机译:光动力疗法的机制:在K562细胞上的光敏剂和细胞定位

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This paper proposes to explore the pattern of lymphoblastic cell line K562 cells death, the effects on their cell cycle induced by 5,10,15,20-tetra-p-sulphonato-phenyl-porphyrin-based photodynamic therapy (TS4PP-PDT). Flow cytometry combined with Annexin V-FITC/PI labeling was used to detect the pattern of K562 cells' death induced by TS4PP-PDT. These effects frequently lead to induction of apoptosis by the mitochondrial pathway involving caspases. The transmission electron microscope (TEM) and confocal laser scanning microscopy (CLSM) were used to detect the localization and time-biodistribution of sensitizers in the cells. After 1 h of TS4PP administration, the sensitizer shows a non-uniform distribution, following that after 4h of administration, the sensitizer to be localized in some cellular targets and an increased fluorescence intensity is being detected. After 8 h and 24 h post-administration, the sensitizer is released from the cells and the light-irradiation (He-Ne laser, &lgr;=632.8 nm) could start. Immediately after irradiation, many typical apoptotic bodies were seen in the cells treated. Most of the cells treated were necrotic at 24 hours following irradiation.
机译:本文提出探讨淋巴细胞系K562细胞死亡的模式,对其细胞周期的影响由5,10,15,20-四硫化苯基 - 苯基 - 卟啉基光动力疗法(TS4PP-PDT)诱导。流式细胞术与膜蛋白V-FITC / PI标记相结合,用于检测TS4PP-PDT诱导的K562细胞死亡的模式。这些效果经常导致涉及胱天蛋白酶的线粒体途径诱导细胞凋亡。透射电子显微镜(TEM)和共聚焦激光扫描显微镜(CLSM)用于检测细胞中敏化剂的定位和时间 - 生物分布。在TS4PP给药1小时后,敏化剂显示出不均匀的分布,之后施用后4小时,敏感剂被检测到一些细胞靶标和增加的荧光强度。在施用后8小时和24小时后,敏感剂从细胞中释放,光辐射(He-Ne激光,&Lgr; = 632.8nm)。在照射后立即,在治疗细胞中看到许多典型的凋亡体。在照射后24小时治疗的大多数细胞是坏死。

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