Suppr超能文献

Ca 依赖性和细胞膜电穿孔修复后的动力学。

Ca dependence and kinetics of cell membrane repair after electropermeabilization.

机构信息

Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA 23508, USA.

Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA 23508, USA; Institute for Digestive System Research, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania.

出版信息

Biochim Biophys Acta Biomembr. 2022 Feb 1;1864(2):183823. doi: 10.1016/j.bbamem.2021.183823. Epub 2021 Nov 25.

Abstract

Electroporation, in particular with nanosecond pulses, is an efficient technique to generate nanometer-size membrane lesions without the use of toxins or other chemicals. The restoration of the membrane integrity takes minutes and is only partially dependent on [Ca]. We explored the impact of Ca on the kinetics of membrane resealing by monitoring the entry of a YO-PRO-1 dye (YP) in BPAE and HEK cells. Ca was promptly removed or added after the electric pulse (EP) by a fast-step perfusion. YP entry increased sharply after the EP and gradually slowed down following either a single- or a double-exponential function. In BPAE cells permeabilized by a single 300- or 600-ns EP at 14 kV/cm in a Ca-free medium, perfusion with 2 mM of external Ca advanced the 90% resealing and reduced the dye uptake about twofold. Membrane restoration was accomplished by a combination of fast, Ca-independent resealing (τ = 13-15 s) and slow, Ca-dependent processes (τ ~70 s with Ca and ~ 110 s or more without it). These time constants did not change when the membrane damage was doubled by increasing EP duration from 300 to 600 ns. However, injury by microsecond-range EP (300 and 600 μs) took longer to recover even when the membrane initially was less damaged, presumably because of the larger size of pores made in the membrane. Full membrane recovery was not prevented by blocking both extra- and intracellular Ca (by loading cells with BAPTA or after Ca depletion from the reticulum), suggesting the recruitment of unknown Ca-independent repair mechanisms.

摘要

电穿孔,特别是纳秒脉冲电穿孔,是一种在不使用毒素或其他化学物质的情况下生成纳米级细胞膜损伤的有效技术。细胞膜完整性的恢复需要几分钟的时间,并且仅部分依赖于[Ca]。我们通过监测 YO-PRO-1 染料(YP)在 BPAE 和 HEK 细胞中的进入,探索了 Ca 对膜重封动力学的影响。在电脉冲(EP)后,通过快速分步灌流迅速去除或添加 Ca。YP 进入在 EP 后急剧增加,并遵循单指数或双指数函数逐渐减慢。在无 Ca 介质中,用 14 kV/cm 的单个 300 或 600 ns EP 使 BPAE 细胞穿孔时,用 2 mM 外部 Ca 进行灌流可加速 90%的重封,并将染料摄取减少约两倍。膜的恢复是通过快速的、Ca 独立的重封(τ=13-15 s)和缓慢的、Ca 依赖性的过程(有 Ca 时τ约为 70 s,无 Ca 时τ约为 110 s 或更长时间)的组合来实现的。当通过将 EP 持续时间从 300 增加到 600 ns 将膜损伤增加一倍时,这些时间常数没有改变。然而,由于在膜中形成的孔较大,微秒范围的 EP(300 和 600 μs)造成的损伤需要更长的时间才能恢复,即使膜最初受到的损伤较小。完全的膜恢复不会被阻止细胞内和细胞外 Ca(通过用 BAPTA 装载细胞或从网状结构中耗尽 Ca),这表明招募了未知的 Ca 独立修复机制。

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