用荧光测定法评估核糖酸、叶绿素铜、三氯氧磷和可溶性吲哚啉对培养中的 A549 细胞生长特性的影响

Q4 Medicine
L. Romodin, E. Yashkina, A.A. Moskovskij
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引用次数: 0

摘要

目前,细胞培养是生物研究中最常用的实验模型系统。然而,要正确规划使用这一模型系统的研究,必须考虑到许多方面。因此,要想正确评估辐射防护药物对细胞的影响,首先必须研究这些物质对培养细胞特性的影响。而使用平板阅读器工作的主要特性是细胞粘附在平板底部的能力和细胞增殖速度。这项工作致力于研究人类核糖酸(肌苷)、叶绿素铜、trolox 和吲哚啉,以及以 A549 细胞系--人类肺腺癌--为基础的培养物中细胞的生长特性。核黄素、叶绿素和铜绿素是很有前途的化合物,可以研究它们的辐射防护特性。吲哚啉是一种经典的辐射防护剂。这一过程使用了含有酒石酸的水溶性形式,使吲哚啉溶于水。实验包括将 A549 细胞在浓度为 2 mM 的核糖甙(肌苷)、叶绿素铜、Trolox 或酒石酸溶液中,或在 2 mM 酒石酸和 1.9 mM 吲哚啉的混合物中培养 24 小时,然后根据 Hoechst-33342 染料的荧光,评估与未添加这些物质培养的细胞相比,样品中的细胞含量。另一项叶绿素实验是将叶绿素附着在片剂底部的细胞培养 2.5 小时,浓度范围为 50-500 μM,然后评估片剂中剩余细胞的含量。据统计,与对照组相比,所有研究物质都能明显降低样品中的细胞含量。叶绿素样本中的细胞含量下降幅度最大,而核糖核苷酸样本中的细胞含量下降幅度最小。将已粘附的细胞放入浓度为 50-500 μM 的叶绿素溶液中培养的结果表明,这种物质对 A549 系细胞的粘附性有剂量依赖性的抑制作用。同时,与对照样品相比,浓度为 50 μM 的叶绿素在统计意义上显著降低了清洗片剂孔后样品中的细胞含量。从统计学角度看,含有吲哚啉和酒石酸混合物的样品中细胞含量的减少比单独在酒石酸溶液中培养所造成的细胞含量的减少要明显得多。也就是说,公认的抗辐射剂吲哚林对 A549 细胞株的生长特性有明显的抑制作用。根据所获得的信息,我们可以得出这样的结论:在计划今后对本研究中的物质进行细胞培养模型研究时,有必要考虑到它们会抑制细胞培养的生长这一事实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fluorimetric Evaluation of the Effect of Riboxin, Copper Chlorophyllin, Trolox and the Soluble form of Indralin on the Growth Properties of A549 Cells in Culture
Currently, cell cultures are most often used as an experimental model system in biological research. However, to correctly plan studies using this model system, many aspects must be taken into account. Thus, to be able to correctly assess the effect of radioprotective drugs on cells, it is first necessary to study the effect of these substances on the properties of cells in culture. And the main property for work using plate readers is the ability of cells to adhere to the bottom of the plate and the rate of cell proliferation. This work is devoted to the study of human riboxin (inosine), copper chlorophyllin, trolox and indralin, the growth properties of cells in a culture based on the A549 cell line - human lung adenocarcinoma. Riboxin, chlorophyllin and trolox are promising compounds that make it possible to study their radioprotective properties. Indralin is a reference classic radioprotector. This process used a water-soluble form containing tartaric acid to allow indralin to dissolve in water. The experiment consisted of incubating A549 cells for 24 hours in a solution of riboxin (inosine), copper chlorophyllin, Trolox or tartaric acid at a concentration of 2 mM or in a mixture of 2 mM tartaric acid and 1.9 mM indralin, followed by assessment of the cell content in the samples compared to cells incubated without the addition of these substances, based on the fluorescence of the Hoechst-33342 dye. An additional experiment with chlorophyllin consisted in incubating cells with chlorophyllin already attached to the bottom of the tablet in the concentration range of 50–500 μM for 2.5 hours, followed by an assessment of the content of the remaining cells in the tablet. All studied substances statistically significantly reduced the cell content in the samples compared to the control. The greatest decrease in cell content was observed in the sample with chlorophyllin, and the least – with riboxin. As a result of additional experience in incubating already attached cells in chlorophyllin solution with concentrations of 50–500 μM, it was shown that this substance dose-dependently inhibits the adhesive properties of cells of the A549 line. At the same time, chlorophyllin already at a concentration of 50 μM statistically significantly reduced the cell content in the sample after washing the wells of the tablet compared with the control sample. The decrease in cell content in the sample containing a mixture of indralin and tartaric acid was statistically significantly more pronounced than that caused by incubation in a solution of tartaric acid alone. That is, the recognized radioprotector indralin demonstrated a pronounced inhibition of the growth properties of the A549 cell line. Based on the information obtained, we can conclude that when planning future studies of the substances studied in this work on a cell culture model, it is necessary to take into account the fact that they inhibit the growth of the cell culture.
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来源期刊
Medical Radiology and Radiation Safety
Medical Radiology and Radiation Safety Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
0.40
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