二极管808 nm GaAlAs低功率激光对人肝癌细胞体外增殖的抑制作用及其可能机制

Yi-Hsiang Liu, Chiung-Chi Cheng, Chin-Chin Ho, Ren-Jeng Pei, Karen Ying Lee, Kun-Tu Yeh, You Chan, Yih-Shyong Lai
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引用次数: 0

摘要

低功率激光照射在医学领域得到了广泛的应用。从基础研究来看,LPLI可以促进DNA合成,提高人体细胞的增殖率。但关于LPLI对人类肝脏或肝癌细胞影响的数据很少。细胞骨架在细胞功能中起着重要作用,因此涉及许多人类肝脏疾病的发病机制,包括恶性肿瘤。在我们之前的研究中,我们发现人肝细胞中细胞角蛋白分子的稳定性与秋水仙碱影响的完整微管网络有关。在本研究中,我们将探讨LPLI对人肝癌细胞系HepG2和J-5细胞增殖的影响。此外,我们还分析了在LPLI作用下细胞角蛋白和synemin(中间丝相关蛋白之一)的稳定性,以评估LPLI影响人肝癌细胞增殖的可能机制。实验中,HepG2和J-5细胞在24孔板中培养24小时。用130 mW二极管808 nm GaAlAs连续波激光器在不同时间间隔照射后,计数细胞数。Western blot和免疫荧光染色检测PCNA、细胞角蛋白和synemin的表达和分布。通过细胞计数和PCNA表达测定细胞增殖情况。研究了细胞角蛋白和联蛋白的组织和表达,以确定LPLI对细胞骨架稳定性的影响。结果显示,LPLI可抑制HepG2和J-5细胞的增殖,使细胞数量减少,PCNA表达减少。HepG2和J-5分别在90秒和120秒的曝光时间(能量密度分别为5.85 J/cm2和7.8 J/cm2)下达到最大效果。HepG2和J-5细胞在该剂量下细胞数量减少率分别为72%和66%。此外,激光照射使这些细胞的中间丝结构紊乱。中间丝相关蛋白synemin的表达也减少。本研究有两个重要发现:(1)二极管808 nm GaAlAs连续波激光对人肝癌细胞系HepG2和J-5的增殖有抑制作用。(2)其抑制机制可能与激光照射导致synemin表达下调和细胞角蛋白组织改变有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of diode 808 nm GaAlAs low-power laser irradiation on inhibition of the proliferation of human hepatoma cells in vitro and their possible mechanism.

Low-power laser irradiation (LPLI) has come into a wide range of use in medical field. Considering basic research, LPLI can enhance DNA synthesis and increases proliferation rate of human cells. But only a few data about the effects of LPLI on human liver or hepatoma cells are available. The cytoskeleton plays important roles in cell function and therefore is implicated in the pathogenesis of many human liver diseases, including malignant tumors. In our previous study, we found the stability of cytokeratin molecules in human hepatocytes was related to the intact microtubule network that was influenced by colchicine. In this study, we are going to search the effect of LPLI on proliferation of human hepatoma cell line HepG2 and J-5 cells. In addition, the stability of cytokeratin and synemin (one of the intermediate filament-associated proteins) were analyzed under the action of LPLI to evaluate the possible mechanism of LPLI effects on proliferation of human hepatoma cells. In experiment, HepG2 and J-5 cells were cultured in 24-well plate for 24 hours. After irradiation by 130 mW diode 808 nm GaAlAs continue wave laser in different time intervals, the cell numbers were counted. Western blot and immunofluorescent staining examined the expression and distribution of PCNA, cytokeratin and synemin. The cell number counting and PCNA expression were evaluated to determine the proliferation. The organization and expression of cytokeratin and synemin were studied to identify the stability of cytoskeleton affected by LPLI. The results revealed that proliferation of HepG2 and J-5 cells was inhibited by LPLI since the cell number and PCNA expression was reduced. Maximal effect was achieved with 90 and 120 seconds of exposure time (of energy density 5.85 J/cm2 and 7.8 J/cm2, respectively) for HepG2 and J-5, respectively. The decreased ratio of cell number by this dose of irradiation was 72% and 66% in HepG2 and J-5 cells, respectively. Besides that, the architecture of intermediate filaments in these cells was disorganized by laser irradiation. The expression of intermediate filament-associated protein, synemin, was also reduced. Two significant findings are raised in this study: (1) Diode 808 nm GaAlAs continuous wave laser has an inhibitory effect on the proliferation of human hepatoma cells line HepG2 and J-5. (2) The mechanism of inhibition might be due to down-regulation of synemin expression and alteration of cytokeratin organization that was caused by laser irradiation.

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