White Jody A, Blackmore Peter F, Schoenbach Karl H, Beebe Stephen J
Biomedical Sciences Program, Old Dominion University and Eastern Virginia Medical School, Norfolk, Virginia, USA.
J Biol Chem. 2004 May 28;279(22):22964-72. doi: 10.1074/jbc.M311135200. Epub 2004 Mar 16.
Nanosecond pulsed electric fields (nsPEFs) are hypothesized to affect intracellular structures in living cells providing a new means to modulate cell signal transduction mechanisms. The effects of nsPEFs on the release of internal calcium and activation of calcium influx in HL-60 cells were investigated by using real time fluorescent microscopy with Fluo-3 and fluorometry with Fura-2. nsPEFs induced an increase in intracellular calcium levels that was seen in all cells. With pulses of 60 ns duration and electric fields between 4 and 15 kV/cm, intracellular calcium increased 200-700 nM, respectively, above basal levels (approximately 100 nM), while the uptake of propidium iodide was absent. This suggests that increases in intracellular calcium were not because of plasma membrane electroporation. nsPEF and the purinergic agonist UTP induced calcium mobilization in the presence and absence of extracellular calcium with similar kinetics and appeared to target the same inositol 1,4,5-trisphosphate- and thapsigargin-sensitive calcium pools in the endoplasmic reticulum. For cells exposed to either nsPEF or UTP in the absence of extracellular calcium, there was an electric field-dependent or UTP dose-dependent increase in capacitative calcium entry when calcium was added to the extracellular media. These findings suggest that nsPEFs, like ligand-mediated responses, release calcium from similar internal calcium pools and thus activate plasma membrane calcium influx channels or capacitative calcium entry.
纳秒级脉冲电场(nsPEFs)被认为会影响活细胞的细胞内结构,从而提供一种调节细胞信号转导机制的新方法。通过使用Fluo-3实时荧光显微镜和Fura-2荧光测定法,研究了nsPEFs对HL-60细胞内钙释放和钙内流激活的影响。nsPEFs诱导所有细胞内钙水平升高。在脉冲持续时间为60纳秒且电场强度在4至15 kV/cm之间时,细胞内钙分别比基础水平(约100 nM)升高200 - 700 nM,同时不存在碘化丙啶摄取。这表明细胞内钙的增加并非由于质膜电穿孔。nsPEF和嘌呤能激动剂UTP在有无细胞外钙的情况下均以相似的动力学诱导钙动员,并且似乎靶向内质网中相同的1,4,5 - 三磷酸肌醇和毒胡萝卜素敏感的钙池。对于在无细胞外钙的情况下暴露于nsPEF或UTP的细胞,当向细胞外培养基中添加钙时,存在电场依赖性或UTP剂量依赖性的钙池性钙内流增加。这些发现表明,nsPEFs与配体介导的反应一样,从相似的细胞内钙池中释放钙,从而激活质膜钙内流通道或钙池性钙内流。