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三维荧光显微镜探测血卟啉单甲醚-组氨酸氯化物光动力治疗诱导的人口腔癌细胞细胞器结构改变。

Structural alterations in cell organelles induced by photodynamic treatment with chlorin p -histamine conjugate in human oral carcinoma cells probed by 3D fluorescence microscopy.

机构信息

Industrial Waste Utilization, Nano and Biomaterials, CSIR - Advanced Materials and Processes Research Institute (AMPRI), Bhopal, India.

Laser Biomedical Applications Division, Raja Ramanna Center for Advanced Technology Indore, Madhya Pradesh, India.

出版信息

Luminescence. 2023 Jul;38(7):1175-1184. doi: 10.1002/bio.4307. Epub 2022 Jun 28.

DOI:10.1002/bio.4307
PMID:35698308
Abstract

We have explored the intracellular cell organelle's structural alterations after photodynamic treatment with chlorin p -histamine conjugate (Cp -his) in human oral cancer cells. Herein, the cells were treated with Cp -his (10 μm) and counterstained with organelle-specific fluorescence probes to find the site of intracellular localization using confocal microscopy. For photodynamic therapy (PDT), the cells were exposed to ~30 kJ/m red light (660 ± 20 nm) to induce ~90% cytotoxicity. We used the three-dimensional (3D) image reconstruction approach to analyze the photodynamic damage to cell organelles. The result showed that Cp -his localized mainly in the endoplasmic reticulum (ER) and lysosomes but not in mitochondria and Golgi apparatus (GA). The 3D model revealed that in necrotic cells, PDT led to extensive fragmentation of ER and fragmentation and swelling of GA as well. Results suggest that the indirect damage to GA occurred due to loss of connection between ER and GA. Moreover, in damaged cells with no sign of necrosis, the perinuclear ER appeared condensed and surrounded by several small clumps at the peripheral region of the cell, and the GA was observed to form a single condensed structure. Since these structural changes were associated with apoptotic cell death, it is suggested that the necrotic and apoptotic death induced by PDT with Cp -his is determined by the severity of damage to ER and indirect damage to GA. The results suggest that the indirect damage to cell organelle apart from the sites of photosensitizer localization and the severity of damage at the organelle level contribute significantly to the mode of cell death in PDT.

摘要

我们研究了光敏剂氯卟啉组胺缀合物(Cp-his)对人口腔癌细胞的光动力作用后细胞内细胞器的结构变化。在此,用 Cp-his(10μm)处理细胞并用细胞器特异性荧光探针复染,并用共聚焦显微镜找到细胞内定位的位置。对于光动力疗法(PDT),用~30kJ/m 的红光(660±20nm)照射细胞以诱导约 90%的细胞毒性。我们使用三维(3D)图像重建方法分析细胞细胞器的光动力损伤。结果表明,Cp-his 主要定位于内质网(ER)和溶酶体,但不在线粒体和高尔基体(GA)中。3D 模型显示,在坏死细胞中,PDT 导致 ER 广泛碎片化以及 GA 碎片化和肿胀。结果表明,由于 ER 和 GA 之间的连接丢失,间接导致 GA 损伤。此外,在没有坏死迹象的受损细胞中,核周 ER 出现浓缩,在细胞外周区域周围有几个小团块,GA 形成单个浓缩结构。由于这些结构变化与细胞凋亡死亡有关,因此,Cp-his 诱导的 PDT 导致的坏死和凋亡死亡取决于 ER 损伤的严重程度和对 GA 的间接损伤。结果表明,除了光敏剂定位部位和细胞器水平损伤的严重程度之外,对细胞细胞器的间接损伤对 PDT 中的细胞死亡方式有重要贡献。

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