Kamoshima Yuuta, Terasaka Shunsuke, Kuroda Satoshi, Iwasaki Yoshinobu
Department of Neurosurgery, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Neurol Res. 2011 Sep;33(7):739-46. doi: 10.1179/1743132810Y.0000000001.
Photodynamic therapy (PDT) using 5-aminolevulinic acid (5-ALA) is a new therapeutic modality for malignant glioma. This study is designed to evaluate acute morphological and histological changes of glioma cells after 5-ALA mediated PDT using fluorescence microscopy and three-dimensional spheroid models.
Monolayer cultures and spheroids (small and large sizes) of C6 (rat glioma cell line) and U251MG (human glioma cell line) cells were co-incubated for 4 hours with 5-ALA (100 μg/ml) and irradiated using a diode laser (635±5 nm, 5-100 mW/cm(2), and total light dose 2.5-50 J/cm(2)). Growth kinetics of the spheroids were followed for 7 days after PDT and morphological changes were assessed by phase contrast microscopy. In addition to hematoxylin and eosin and the terminal deoxynucleotidyl transferase-mediated dUTP-FITC nick end-labeling, various fluorescent dyes including calcein AM, ethidium homodimer-1 (EthD-1), annexin V-FITC, propidium iodide and Hoechst 33342, were used to clarify the mechanism of cell death after PDT.
Although PDT spheroids of both cell lines showed growth inhibition during the first few days, resumption of spheroid growth on day 3 after irradiation was observed in most spheroids. Hematoxylin and eosin staining showed cells with condensed chromatin within the superficial layer of the PDT spheroids. In the PDT groups, monolayer cells in the irradiated area were negative for calcein AM and clearly positive for EthD-1. In C6 PDT spheroids, the outer layer of the spheroid was negative for calcein AM and positive for EthD-1. In monolayer cells, cells in the irradiation area in PDT groups were positive for propidium iodide and negative for Hoechst 33342.
Light and fluorescence microscopic findings suggested necrotic cell death as an anti-tumor effect in the acute phase after PDT. These findings were observed in both C6 and U251MG monolayer culture cells and spheroids. Although various total light doses resulted in significant differences in the growth rate of spheroids after PDT, resumption of spheroid growth occurred in most spheroids.
使用5-氨基酮戊酸(5-ALA)的光动力疗法(PDT)是恶性胶质瘤的一种新治疗方式。本研究旨在利用荧光显微镜和三维球体模型评估5-ALA介导的PDT后胶质瘤细胞的急性形态学和组织学变化。
将C6(大鼠胶质瘤细胞系)和U251MG(人胶质瘤细胞系)细胞的单层培养物和球体(大小不同)与5-ALA(100μg/ml)共孵育4小时,然后用二极管激光照射(635±5nm,5-100mW/cm²,总光剂量2.5-50J/cm²)。PDT后跟踪球体的生长动力学7天,并通过相差显微镜评估形态学变化。除苏木精和伊红以及末端脱氧核苷酸转移酶介导的dUTP-FITC缺口末端标记外,还使用包括钙黄绿素AM、碘化乙啶同型二聚体-1(EthD-1)、膜联蛋白V-FITC、碘化丙啶和Hoechst 33342在内的各种荧光染料来阐明PDT后细胞死亡的机制。
尽管两种细胞系的PDT球体在最初几天都显示出生长抑制,但在大多数球体中观察到照射后第3天球体生长恢复。苏木精和伊红染色显示PDT球体表层内有染色质浓缩的细胞。在PDT组中,照射区域的单层细胞钙黄绿素AM呈阴性,EthD-1呈明显阳性。在C6 PDT球体中,球体外层钙黄绿素AM呈阴性,EthD-1呈阳性。在单层细胞中,PDT组照射区域的细胞碘化丙啶呈阳性,Hoechst 33342呈阴性。
光镜和荧光显微镜检查结果表明,坏死性细胞死亡是PDT急性期的抗肿瘤效应。在C6和U251MG单层培养细胞及球体中均观察到这些结果。尽管不同的总光剂量导致PDT后球体生长速率存在显著差异,但大多数球体仍恢复了生长。