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ETM study of electroporation influence on cell morphology in human malignant melanoma and human primary gingival fibroblast cells

机译:ETM研究电穿孔对人恶性黑色素瘤和人原发性牙龈成纤维细胞的细胞形态的影响

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Objective:To estimate electroporation (EP) influence on malignant and normal cells.Methods:Two cell lines including human malignant melanoma (Me-45) and normal human gingival fibroblast (HGFs) were used. EP parameters were the following:250,1000,1750,2500 V/cm;50 μs by5 impulses for every case. The viability of cells after EP was estimated byMTT assay. The ultrastructural analysis was observed by transmission electron microscope (ZeissEM900). Results:In the current study we observed the intracellular effect followingEP on Me-45 and HGF cells. At the conditions applied, we did not observe any significant damage of mitochondrial activity in both cell lines treated byEP. Conversely, we showed thatEP in some conditions can stimulate cells to proliferation. Some changes induced byEP were only visible in electron microscopy. In fibroblast cells we observed significant changes in lower parameters ofEP (250 and1000 V/cm). After applying higher electric field intensities (2500 V/cm) we detected many vacuoles, myelin-like bodies and swallowed endoplasmic reticulum. In melanoma cells such strong pathological modifications afterEP were not observed, in comparison with control cells. The ultrastructure of both treated cell lines was changed according to the applied parameters ofEP.Conclusions:We can claim thatEP conditions are cell line dependent. In terms of the intracellular morphology, human fibroblasts are more sensitive to electric field as compared with melanoma cells. Optimal conditions should be determined for each cell line. Summarizing our study, we can conclude thatEP is not an invasive method for human normal and malignant cells. This technique can be safely applied in chemotherapy for delivering drugs into tumor cells.
机译:目的:评估电穿孔(EP)对恶性和正常细胞的影响。方法:使用两种细胞系,包括人恶性黑色素瘤(Me-45)和正常人牙龈成纤维细胞(HGF)。 EP参数如下:250,1000,1750,2500 V / cm;每种情况下5次脉冲50μs。通过MTT分析评估EP后细胞的存活力。通过透射电子显微镜(ZeissEM900)观察超微结构分析。结果:在目前的研究中,我们观察到EP后对Me-45和HGF细胞的细胞内作用。在所应用的条件下,我们在用EP处理的两种细胞系中均未观察到线粒体活性的任何显着损害。相反,我们表明EP在某些条件下可以刺激细胞增殖。 EP诱发的某些变化仅在电子显微镜下可见。在成纤维细胞中,我们观察到较低的EP参数(250和1000 V / cm)发生了显着变化。在施加更高的电场强度(2500 V / cm)后,我们检测到许多液泡,髓鞘样体和吞咽的内质网。与对照细胞相比,在黑色素瘤细胞中未观察到EP后如此强烈的病理改变。根据EP的应用参数改变了两种处理过的细胞系的超微结构。结论:我们可以认为EP的条件与细胞系有关。就细胞内形态而言,与黑色素瘤细胞相比,人类成纤维细胞对电场更敏感。应该为每个细胞系确定最佳条件。总结我们的研究,我们可以得出结论,EP不是对人类正常和恶性细胞的侵入性方法。该技术可以安全地用于化学疗法中,以将药物输送到肿瘤细胞中。

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    Department of Medical Biochemistry, Medical University, Chalubinskiego 10 St., 50-368 Wroclaw, Poland;

    Department of General Zoology, Zoological Institute, University of Wroclaw, Sienkiewicza 21 St., 50-335 Wroclaw, Poland;

    Department of Medical Biochemistry, Medical University, Chalubinskiego 10 St., 50-368 Wroclaw, Poland;

    Department of Medical Biochemistry, Medical University, Chalubinskiego 10 St., 50-368 Wroclaw, Poland;

    Department of Medical Biochemistry, Medical University, Chalubinskiego 10 St., 50-368 Wroclaw, Poland;

    Institute of Biomedical Engineering and Instrumentation, Wroclaw University of Technology, ul. Wybrzeze Wyspianskiego 27, 50-370 Wroclaw, Poland;

    Department of Medical Biochemistry, Medical University, Chalubinskiego 10 St., 50-368 Wroclaw, Poland;

    Department of Medical Biochemistry, Medical University, Chalubinskiego 10 St., 50-368 Wroclaw, Poland;

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  • 入库时间 2022-08-19 03:58:34
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