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Changes in Protein Expression of U937 and Jurkat Cells Exposed to Nanosecond Pulsed Electric Fields

机译:U937蛋白表达的变化和暴露于纳秒脉冲电场的Jurkat细胞

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Application of nanosecond pulsed electric fields (nsPEF) to various biological cell lines has been to shown to cause many diverse effects, including poration of the plasma membrane, depolarization of the mitochondrial membrane, blebbing, apoptosis, and intracellular calcium bursts. The underlying mechanism(s) responsible for these diverse responses are poorly understood. Of specific interest in this paper are the long-term effects of nsPEF on cellular processes, including the regulation of genes and production of proteins. Previous studies have reported transient activation of select signaling pathways involving mitogen-activated protein kinases (MAPKs), protein phosphorylation and downstream gene expression following nsPEF application. We hypothesize that nsPEF represents a unique stimulus that could be used to externally modulate cellular processes. To validate our hypothesis, we performed a series of cuvette-based exposures at 10 and 600ns pulse widths using a custom Blumlien line pulser system. We measured acute changes in the plasma membrane structure using flow cytometry by tracking phosphatidylserine externalization via FITC-Annexin V labeling and poration via propidium iodide uptake. We then compared these results to viability of the cells at 24 hours post exposure using MTT assay and changes in the MAPK family of proteins at 8 hours post-exposure using Luminex assay. By comparing exposures at 10 and 600ns duration, we found that most MAPK family-protein expression increased in Jurkat and U937 cell lines following exposure and compared well with drops in viability and changes in plasma membrane asymmetry. What proved interesting is that some MAPK family proteins (e.g. p53, STAT1), were expressed in one cell line, but not the other. This difference may point to an underlying mechanism for observed difference in cellular sensitivity to nsPEFinduced stresses.
机译:纳秒脉冲电场(NPEF)在各种生物细胞系中的应用已经显示出造成许多不同的效果,包括质膜的血浆,线粒体膜的去极化,肺泡,细胞凋亡和细胞内钙爆发。负责这些多种反应的潜在机制尚不清楚。本文的具体兴趣是NPEF对细胞过程的长期影响,包括调节基因和蛋白质的产生。先前的研究报告了涉及丝裂原激活蛋白激酶(MAPK),蛋白质磷酸化和下游基因表达后的选择信号通路的瞬时激活。我们假设NSPEF表示可以用于外部调制蜂窝过程的独特刺激。为了验证我们的假设,我们在10和600NS脉冲宽度下执行了一系列基于比色皿的曝光,使用自定义Blumlien线脉冲系统。通过通过碘化丙啶丙烷丙烷丙烷的磷脂酰综合体,通过流式细胞术测量了使用流式细胞术的急性变化。然后,将这些结果与通过MTT测定的24小时在暴露后24小时的曝光后24小时的可存活率和使用LuminX测定后8小时的Mapk系列蛋白质的变化。通过比较10和600ns持续时间的曝光,我们发现大多数MAPK家族蛋白表达在接触后的Jurkat和U937细胞系中增加,并在活力下的液滴和血浆膜不对称的变化进行比较。有趣的是一些Mapk家族蛋白(例如p53,stat1),在一种细胞系中表达,但不是另一个细胞系列。这种差异可以指向观察到对Nspefinduced应力的细胞敏感性差异的潜在机制。

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