Tajiri H, Hayakawa A, Matsumoto Y, Yokoyama I, Yoshida S
Department of Internal Medicine, National Cancer Center Hospital East, Kashiwa, Chiba, Japan.
Cancer Lett. 1998 Jun 19;128(2):205-10. doi: 10.1016/s0304-3835(98)00066-4.
For photodynamic therapy (PDT), human squamous cell carcinoma cells (HSC-2) were treated with 3 microg/ml of photofrin 24 h prior to irradiating the cultures with the excimer dye laser at a dose of 2 J/cm2. Extensive DNA fragmentation was recognized within 2 h of PDT. The proportion of cells with DNA fragmentation on flow cytometric analysis was significantly increased to 44 and 78% at 1 and 2 h after PDT, respectively, compared to control groups. Confocal laser scanning microscopy revealed a slight change in the intracellular Ca2+ concentration occurring at 30 min after PDT and a subsequent marked increase in the Ca2+ concentration 1-2 h after PDT, but no change was observed in the cells exposed to laser irradiation alone and to photofrin alone and in the cells immediately after PDT. These findings suggest that an increase in the intracellular Ca2+ concentration may play an important role in the induction of PDT-induced apoptosis.
对于光动力疗法(PDT),在用人准分子染料激光以2 J/cm²的剂量照射培养物之前24小时,将人鳞状细胞癌细胞(HSC-2)用3微克/毫升的血卟啉衍生物进行处理。在光动力疗法后2小时内可识别出广泛的DNA片段化。与对照组相比,在光动力疗法后1小时和2小时,流式细胞术分析显示具有DNA片段化的细胞比例分别显著增加至44%和78%。共聚焦激光扫描显微镜显示,光动力疗法后30分钟细胞内Ca²⁺浓度有轻微变化,在光动力疗法后1 - 2小时Ca²⁺浓度随后显著增加,但在单独接受激光照射的细胞、单独接受血卟啉衍生物处理的细胞以及光动力疗法后即刻的细胞中未观察到变化。这些发现表明细胞内Ca²⁺浓度的增加可能在光动力疗法诱导的细胞凋亡中起重要作用。