Ibey Bennett L, Pakhomov Andrei G, Gregory Betsy W, Khorokhorina Vera A, Roth Caleb C, Rassokhin Mikhail A, Bernhard Joshua A, Wilmink Gerald J, Pakhomova Olga N
Radio Frequency Radiation Branch, 711th Human Performance Wing, Air Force Research Laboratory, Brooks City-Base, San Antonio, TX, USA.
Biochim Biophys Acta. 2010 Nov;1800(11):1210-9. doi: 10.1016/j.bbagen.2010.07.008. Epub 2010 Aug 3.
Nanosecond electric pulses (EP) disrupt cell membrane and organelles and cause cell death in a manner different from the conventional irreversible electroporation. We explored the cytotoxic effect of 10-ns EP (quantitation, mechanisms, efficiency, and specificity) in comparison with 300-ns, 1.8- and 9-μs EP.
Effects in Jurkat and U937 cells were characterized by survival assays, DNA electrophoresis and flow cytometry.
10-ns EP caused apoptotic or necrotic death within 2-20 h. Survival (S, %) followed the absorbed dose (D, J/g) as: S=alphaD((-K)), where coefficients K and alpha determined the slope and the "shoulder" of the survival curve. K was similar in all groups, whereas alpha was cell type- and pulse duration-dependent. Long pulses caused immediate propidium uptake and phosphatidylserine (PS) externalization, whereas 10-ns pulses caused PS externalization only.
1.8- and 9-μs EP cause cell death efficiently and indiscriminately (LD₅₀ 1-3 J/g in both cell lines); 10-ns EP are less efficient, but very selective (LD₅₀ 50-80 J/g for Jurkat and 400-500 J/g for U937); 300-ns EP show intermediate effects. Shorter EP open propidium-impermeable, small membrane pores ("nanopores"), triggering different cell death mechanisms.
Nanosecond EP can selectively target certain cells in medical applications like tumor ablation.
纳秒级电脉冲(EP)会破坏细胞膜和细胞器,并以一种不同于传统不可逆电穿孔的方式导致细胞死亡。我们比较了10纳秒EP与300纳秒、1.8微秒和9微秒EP的细胞毒性作用(定量、机制、效率和特异性)。
通过存活测定、DNA电泳和流式细胞术来表征对Jurkat和U937细胞的影响。
10纳秒EP在2至20小时内导致凋亡或坏死性死亡。存活率(S,%)与吸收剂量(D,J/g)的关系为:S = αD^(-K),其中系数K和α决定了存活曲线的斜率和“肩部”。所有组的K值相似,而α值则取决于细胞类型和脉冲持续时间。长脉冲会立即导致碘化丙啶摄取和磷脂酰丝氨酸(PS)外化,而10纳秒脉冲仅导致PS外化。
1.8微秒和9微秒EP能高效且无差别地导致细胞死亡(两种细胞系的半数致死剂量均为1 - 3 J/g);10纳秒EP效率较低,但具有高度选择性(Jurkat细胞的半数致死剂量为50 - 80 J/g,U937细胞为400 - 500 J/g);300纳秒EP表现出中等效应。较短的EP会打开对碘化丙啶不可渗透的小膜孔(“纳米孔”),触发不同的细胞死亡机制。
在肿瘤消融等医学应用中,纳秒级EP可以选择性地靶向某些细胞。