Suppr超能文献

纳秒级强脉冲对哺乳动物细胞的选择性细胞毒性

Selective cytotoxicity of intense nanosecond-duration electric pulses in mammalian cells.

作者信息

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

机构信息

Radio Frequency Radiation Branch, 711th Human Performance Wing, Air Force Research Laboratory, Brooks City-Base, San Antonio, TX, USA.

出版信息

Biochim Biophys Acta. 2010 Nov;1800(11):1210-9. doi: 10.1016/j.bbagen.2010.07.008. Epub 2010 Aug 3.

Abstract

BACKGROUND

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.

METHODS

Effects in Jurkat and U937 cells were characterized by survival assays, DNA electrophoresis and flow cytometry.

RESULTS

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.

CONCLUSIONS

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.

GENERAL SIGNIFICANCE

Nanosecond EP can selectively target certain cells in medical applications like tumor ablation.

摘要

背景

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)。

方法

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。

结果

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。

结论

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。

一般意义

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验