[5-氨基乙酰丙酸介导的C6胶质瘤球体光动力疗法]。

Yuuta Kamoshima, Shunsuke Terasaka, Yoshinobu Iwasaki
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引用次数: 0

摘要

背景:5-氨基乙酰丙酸光动力疗法是目前治疗恶性胶质瘤的新方法之一。关于5- ala介导的PDT急性期细胞损伤的机制一直存在争议。本研究观察了C6球形模型5- ala介导的PDT的急性形态学和组织学后遗症,并探讨了急性期细胞损伤机制。方法:不同尺寸的C6球体在100 μ g/ml的5-ALA中孵育4 h,然后用不同总能量(635+/-5 nm, 5-100 mW/cm2,总光剂量2.5-50 J/cm2)的二极管激光器照射。为了研究形态学变化,在PDT前后测量了球体的直径。在PDT后的球体冷冻切片上进行苏木精-伊红和TUNEL检测作为组织学评估。用膜联蛋白V-FITC和碘化丙啶(PI)进行荧光显微镜检查以区分坏死和凋亡。采用单纯激光治疗、单纯ALA治疗和不治疗的对照组进行比较。结果:所有5- ala介导的PDT球体在PDT后立即直径增大。它们增加了浅层区的光透明度,表明细胞膜受到损伤。在2.5 ~ 50 J/cm2的总光剂量范围内,相同大小的球体膨胀率无显著差异。在总光剂量为25 J/cm2的PDT下,大球体比小球体扩张更小(PDT)。结论:本实验中PDT介导的5-ALA对球体模型实验胶质瘤的细胞损伤迅速且显著,PDT后出现急性坏死。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Photodynamic therapy mediated with 5-aminolevulinic acid for C6 glioma spheroids].

Background: The photodynamic therapy using 5-aminolevulinic acid is one of the new therapeutic modalities for malignant glioma yet. There has been a controversy as to the mechanism of cell damage in acute phase induced by 5-ALA-mediated PDT. In this study, acute morphological and histological sequelae of 5-ALA-mediated PDT in the C6 spheroid model were examined and the cell damage mechanism in acute phase was discussed.

Methods: Various sizes of C6 spheroids were incubated for 4 h in 100 microg/ml of 5-ALA and subsequent by irradiated with a diode laser at various total energies (635+/-5 nm, 5-100 mW/cm2, total light dose 2.5-50 J/cm2). For investigating morphological changes, the spheroid's diameter was measured just before and after PDT. Hematoxylin-eosin and TUNEL assays were performed on cryosections of the spheroids after PDT as a histological assessment. Fluorescence microscopic examination was performed using annexin V-FITC and propidium iodide (PI) to distinguish necrosis and apoptosis. Control groups with laser only, ALA only or no treatment were used in comparison.

Results: All spheroids with 5-ALA-mediated PDT enlarged in their diameters immediately after PDT. They increased light transparency in superficial zone, which indicated cell membrane damage. There were no significant differences in the expansion of spheroids of a same size among the total light doses at 2.5-50 J/cm2. Large spheroids were less expanded by PDT at total light dose 25 J/cm2 as compared with small ones (P<0.01). H.E. staining showed condensed nucleus and cytoplasm in the superficial layer. However, these cells were negative for TUNEL staining. The spheroid after 5-ALA-mediated PDT was apparently densely positive for PI staining. Double stains for PI and annexin V-FITC indicated that positive cells for annexin V-FITC were also positive for PI. Only annexin V-FITC-positive cells were scarcely demonstrated. These findings were not seen in any of control groups.

Conclusions: PDT-mediated 5-ALA for experimental glioma using spheroid model in the present in vitro study resulted in rapid and significant cells damage, which indicated acute necrosis just after PDT.

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