Modifications of DAMPs levels in extracellular environment induced by aminolevulinic acid-based photodynamic therapy of esophageal cancer cells.

Beata Čunderlíková, Kristína Klučková, Pavel Babál, Peter Mlkvý, Tibor Teplický
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Abstract

Purpose: Immunogenic cell death plays an important role in anticancer treatment because it combines cell death with appearance of damage associated molecular patterns that have the potential to activate anticancer immunity. Effects of damage associated molecular patterns induced by aminolevulinic acid-based photodynamic therapy were studied mainly on dendritic cells. They have not been deeply studied on macrophages that constitute the essential component of the tumor microenvironment. The aim of this study was to analyze features of esophageal cancer cell death in relation to release capacity of damage associated molecular pattern species, and to test the effect of related extracellular environmental alterations on macrophages.

Material and methods: Esophageal Kyse 450 carcinoma cells were subjected to aminolevulinic acid-based photodynamic therapy at different concentrations of aminolevulinic acid. Resting, IFN/LPS and IL-4 macrophage subtypes were prepared from monocytic THP-1 cell line. Cell death features and macrophage modifications were analyzed by fluorescence-based live cell imaging. ATP and HMGB1 levels in cell culture media were determined by ELISA assays. The presence of lipid peroxidation products in culture media was assessed by spectrophotometric detection of thiobarbituric acid reactive substances.

Results: Aminolevulinic acid-based photodynamic therapy induced various death pathways in Kyse 450 cells that included features of apoptosis, necrosis and ferroptosis. ATP amounts in extracellular environment of treated Kyse 450 cells increased with increasing aminolevulinic acid concentration. Levels of HMGB1, detectable by ELISA assay in culture media, were decreased after the treatment. Aminolevulinic acid-based photodynamic therapy induced lipid peroxidation of cellular structures and increased levels of extracellular lipid peroxidation products. Incubation of resting and IL-4 macrophages in conditioned medium from Kyse 450 cells treated by aminolevulinic acid-based photodynamic therapy induced morphological changes in macrophages, however, comparable alterations were induced also by conditioned medium from untreated cancer cells.

Conclusion: Aminolevulinic acid-based photodynamic therapy leads to alterations in local extracellular levels of damage associated molecular patterns, however, comprehensive studies are needed to find whether they can be responsible for macrophage phenotype modifications.

基于氨基乙酰乙酸的食管癌光动力疗法诱导的细胞外环境中 DAMPs 水平的改变
目的:免疫性细胞死亡在抗癌治疗中发挥着重要作用,因为它将细胞死亡与损伤相关分子模式的出现结合在一起,而损伤相关分子模式有可能激活抗癌免疫。基于氨基乙酰丙酸的光动力疗法诱导的损伤相关分子模式的影响主要是针对树突状细胞进行研究的。而对构成肿瘤微环境重要组成部分的巨噬细胞的研究还不够深入。本研究旨在分析食管癌细胞死亡与损伤相关分子模式物种释放能力有关的特征,并检测相关细胞外环境改变对巨噬细胞的影响:食管 Kyse 450 癌细胞在不同浓度的氨基乙酰丙酸作用下接受氨基乙酰丙酸光动力治疗。用单核细胞 THP-1 细胞系制备静息巨噬细胞、IFN/LPS 巨噬细胞和 IL-4 巨噬细胞亚型。通过荧光活细胞成像分析了细胞死亡特征和巨噬细胞修饰。细胞培养基中的 ATP 和 HMGB1 水平通过酶联免疫吸附试验测定。通过分光光度法检测硫代巴比妥酸活性物质,评估培养基中脂质过氧化产物的存在:结果:基于氨基乙酰丙酸的光动力疗法诱导了 Kyse 450 细胞的多种死亡途径,包括细胞凋亡、坏死和铁沉着。经处理的 Kyse 450 细胞胞外环境中的 ATP 量随着氨基乙酰丙酸浓度的增加而增加。通过酶联免疫吸附试验检测培养基中的 HMGB1 水平,处理后的 HMGB1 水平有所下降。基于氨基乙酰丙酸的光动力疗法诱导了细胞结构的脂质过氧化,并增加了细胞外脂质过氧化产物的水平。将静息巨噬细胞和 IL-4 巨噬细胞置于经氨基乙酰乙酸光动力疗法处理的 Kyse 450 细胞的条件培养基中培养,可诱导巨噬细胞发生形态学变化,但未经处理的癌细胞的条件培养基也会诱导类似的变化:结论:基于氨基乙酰丙酸的光动力疗法会导致局部细胞外损伤相关分子模式水平的改变,但它们是否会导致巨噬细胞表型的改变,还需要进行全面的研究。
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