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Apoptosis by direct electric field (DEF) and nanosecond pulsed electric field (nsPEF) in tumor cells and tumor tissues

机译:通过直接电场(DEF)和纳秒脉冲电场(nsPEF)在肿瘤细胞和肿瘤组织中凋亡

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Pulsed electric field induces cell fusion, electroporation on biological cells. Electroporation them occurs with pulse durations in the order of 0.1-10 ms and electric fields of kV/cm, depending on the cell type and suspension media. Nanosecond pulsed electric fields(nsPEF) are normally with durations of about 1-300 ns with the electric field strength less than 300 kV/cm. The nsPEF is recognized to induce apoptosis in cells by affecting intracellular structures. Apoptosis is expressed in a series of natural enzymatic reactions for the natural elimination of unhealthy, genetically damaged, or otherwise aberrant cells that are not needed or not advantageous to the well-being of the organism. Its markers involve cell shrinkage, activation of intracellular caspase proteases, externalization of phosphatidylserine at the plasma membrane, and fragmentation of DNA. Direct electric fields(DEF) using direct current have been exploited recently to investigate its effects on tumor cells and tissues, but the mechanism of DEF has not been exhibited clearly other than by electroosmosis or pH changes. We show that DEF induces apoptosis in tumor cells cultured as indicated by cell shrinkage, DNA fragmentation and tumor suppression. The DEF effects depend upon current intensity, level of potential and expose time of cell to DEF We also exhibit that the inhibition of tumor growth(anti-tumor effects) correlates incident dose (electrical charge delivered) into tumor tissues in formula. Total electric charge will also be compared in the two cases of nsPEF and DEF approach.
机译:脉冲电场诱导细胞融合,并在生物细胞上进行电穿孔。根据细胞类型和悬浮介质,它们以0.1-10 ms的脉冲持续时间和kV / cm的电场发生电穿孔。纳秒脉冲电场(nsPEF)的持续时间通常为1-300 ns,电场强度小于300 kV / cm。 nsPEF被认为可通过影响细胞内结构来诱导细胞凋亡。凋亡在一系列天然酶反应中表达,用于天然消除不需要或不利于生物体健康的不健康,遗传受损或其他异常细胞。它的标志物包括细胞收缩,细胞内半胱天冬酶的活化,质膜上磷脂酰丝氨酸的外在化和DNA片段化。最近已经使用直流电来研究直流电对肿瘤细胞和组织的作用,但是除电渗透或pH改变外,还没有清楚地显示出其作用机理。我们显示DEF诱导培养的肿瘤细胞凋亡,如细胞收缩,DNA片段化和肿瘤抑制所示。 DEF的作用取决于电流强度,电位水平以及细胞暴露于DEF的时间。我们还显示,肿瘤生长的抑制(抗肿瘤作用)与配方中肿瘤组织的入射剂量(传递的电荷)相关。在nsPEF和DEF方法的两种情况下,还将对总电荷进行比较。

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