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纳秒级脉冲电场(nsPEF)对哺乳动物细胞进行的持久质膜通透化处理。

Long-lasting plasma membrane permeabilization in mammalian cells by nanosecond pulsed electric field (nsPEF).

作者信息

Pakhomov Andrei G, Kolb Juergen F, White Jody A, Joshi Ravindra P, Xiao Shu, Schoenbach Karl H

机构信息

Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, Virginia, USA.

出版信息

Bioelectromagnetics. 2007 Dec;28(8):655-63. doi: 10.1002/bem.20354.

Abstract

The barrier function of plasma membrane in nsPEF-exposed mammalian cells was examined using whole-cell patch-clamp techniques. A specialized setup for nsPEF exposure of individual cells in culture was developed and characterized for artifact-free compatibility with the patch-clamp method. For the first time, our study provides experimental evidence that even a single 60-ns pulse at 12 kV/cm can cause a profound and long-lasting (minutes) reduction of the cell membrane resistance (R(m)), accompanied by the loss of the membrane potential. R(m) measured in GH3, PC-12, and Jurkat cells (but not in HeLa cells) in 80-120 s after nsPEF exposure was decreased about threefold, and its gradual recovery could take 15 min. Multiple pulses enhanced permeabilization, for example, R(m) in GH3 cells fell about 10-fold after a train of five pulses. Within studied limits, permeabilization did not depend on the presence of Ca(2+), Mg(2+), K(+), Cs(+), Cd(2+), EGTA, tetraethylammonium, or 4-aminopyridine in the pipette or bath solutions. Our results supported theoretical model predictions of plasma membrane poration by nsPEF. However, the extended decrease in R(m), assumed to be related to the life span of the pores, and different nsPEF sensitivity of individual cell lines have yet to be explained. The phenomenon of long-lived membrane permeabilization provides new insights on the nature of nsPEF-opened conductance pores and on molecular mechanisms that underlie nsPEF bioeffects.

摘要

使用全细胞膜片钳技术检测了经纳秒级脉冲电场(nsPEF)处理的哺乳动物细胞中质膜的屏障功能。开发了一种用于在培养物中对单个细胞进行nsPEF处理的专门装置,并对其进行了表征,以确保与膜片钳方法兼容且无伪迹。我们的研究首次提供了实验证据,即即使在12 kV/cm下施加单个60 ns脉冲也可导致细胞膜电阻(R(m))显著且持久(数分钟)降低,并伴随着膜电位的丧失。在nsPEF处理后80 - 120 s内,在GH3、PC - 12和Jurkat细胞(但不在HeLa细胞中)中测得的R(m)降低了约三倍,其逐渐恢复可能需要15分钟。多个脉冲增强了通透性,例如,在一串五个脉冲后,GH3细胞中的R(m)下降了约10倍。在所研究的范围内,通透性不依赖于移液管或浴液中Ca(2+)、Mg(2+)、K(+)、Cs(+)、Cd(2+)、乙二醇双四乙酸(EGTA)、四乙铵或4 - 氨基吡啶的存在。我们的结果支持了nsPEF使质膜形成孔道的理论模型预测。然而,R(m)的持续降低(假定与孔道的寿命有关)以及不同细胞系对nsPEF的不同敏感性仍有待解释。长期膜通透性的现象为nsPEF打开的导电孔道的性质以及nsPEF生物效应的分子机制提供了新的见解。

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