Vectorology and Anticancer Therapies, UMR 8203, CNRS, Univ. Paris-Sud, Gustave Roussy, Université Paris-Saclay, 94 805, Villejuif, France.
Department of Information Engineering, Electronics and Telecommunication (DIET), University of Rome "La Sapienza", Rome, 00184, Italy.
Sci Rep. 2017 Oct 12;7(1):13079. doi: 10.1038/s41598-017-12960-w.
Microsecond pulsed electric fields (μsPEF) permeabilize the plasma membrane (PM) and are widely used in research, medicine and biotechnology. For internal membranes permeabilization, nanosecond pulsed electric fields (nsPEF) are applied but this technology is complex to use. Here we report that the endoplasmic reticulum (ER) membrane can also be electropermeabilized by one 100 µs pulse without affecting the cell viability. Indeed, using Ca as a permeabilization marker, we observed cytosolic Ca peaks in two different cell types after one 100 µs pulse in a medium without Ca. Thapsigargin abolished these Ca peaks demonstrating that the calcium is released from the ER. Moreover, IP3R and RyR inhibitors did not modify these peaks showing that they are due to the electropermeabilization of the ER membrane and not to ER Ca channels activation. Finally, the comparison of the two cell types suggests that the PM and the ER permeabilization thresholds are affected by the sizes of the cell and the ER. In conclusion, this study demonstrates that µsPEF, which are easier to control than nsPEF, can permeabilize internal membranes. Besides, μsPEF interaction with either the PM or ER, can be an efficient tool to modulate the cytosolic calcium concentration and study Ca roles in cell physiology.
微秒脉冲电场(μsPEF)可使质膜(PM)穿孔,广泛应用于研究、医学和生物技术领域。为了使内膜穿孔,通常采用纳秒脉冲电场(nsPEF),但该技术使用起来较为复杂。本研究报告称,内质网(ER)膜也可以通过施加一个 100μs 的脉冲而发生电穿孔,而不会影响细胞活力。实际上,我们使用 Ca 作为通透性标记物,在不含 Ca 的培养基中施加一个 100μs 的脉冲后,在两种不同的细胞类型中观察到胞质 Ca 峰。他莫昔芬(thapsigargin)消除了这些 Ca 峰,表明 Ca 是从 ER 中释放出来的。此外,IP3R 和 RyR 抑制剂并未改变这些峰,表明它们是由于 ER 膜的电穿孔而不是 ER Ca 通道的激活所致。最后,两种细胞类型的比较表明,PM 和 ER 的通透性阈值受细胞和 ER 大小的影响。总之,本研究表明,与 nsPEF 相比,更容易控制的 μsPEF 可以使内膜穿孔。此外,μsPEF 与 PM 或 ER 的相互作用,可以成为调节胞质 Ca 浓度的有效工具,并研究 Ca 在细胞生理学中的作用。