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纳秒电脉冲会影响质膜上的一种植物特异性驱动蛋白。

Nanosecond electric pulses affect a plant-specific kinesin at the plasma membrane.

机构信息

Botanical Institute, Karlsruhe Institute of Technology, Kaiserstr. 2, 76128, Karlsruhe, Germany,

出版信息

J Membr Biol. 2013 Dec;246(12):927-38. doi: 10.1007/s00232-013-9594-z. Epub 2013 Sep 24.

Abstract

Electric pulses with high field strength and durations in the nanosecond range (nsPEFs) are of considerable interest for biotechnological and medical applications. However, their actual cellular site of action is still under debate--due to their extremely short rise times, nsPEFs are thought to act mainly in the cell interior rather than at the plasma membrane. On the other hand, nsPEFs can induce membrane permeability. We have revisited this issue using plant cells as a model. By mapping the cellular responses to nsPEFs of different field strength and duration in the tobacco BY-2 cell line, we could define a treatment that does not impinge on short-term viability, such that the physiological responses to the treatment can be followed. We observe, for these conditions, a mild disintegration of the cytoskeleton, impaired membrane localization of the PIN1 auxin-efflux transporter and a delayed premitotic nuclear positioning followed by a transient mitotic arrest. To address the target site of nsPEFs, we made use of the plant-specific KCH kinesin, which can assume two different states with different localization (either near the nucleus or at the cell membrane) driving different cellular functions. We show that nsPEFs reduce cell expansion in nontransformed cells but promote expansion in a line overexpressing KCH. Since cell elongation and cell widening are linked to the KCH localized at the cell membrane, the inverted response in the KCH overexpressor provides evidence for a direct action of nsPEFs, also at the cell membrane.

摘要

高强度、纳秒级持续时间的电脉冲(nsPEFs)在生物技术和医学应用中引起了极大的兴趣。然而,由于其极短的上升时间,nsPEFs 被认为主要作用于细胞内部而不是质膜,因此其实际的细胞作用部位仍存在争议。另一方面,nsPEFs 可以诱导细胞膜通透性。我们使用植物细胞作为模型重新研究了这个问题。通过绘制烟草 BY-2 细胞系中不同场强和持续时间的 nsPEFs 的细胞反应图谱,我们可以定义一种不会影响短期存活率的处理方法,以便可以跟踪处理的生理反应。对于这些条件,我们观察到细胞骨架轻微解体、PIN1 生长素外排转运蛋白的膜定位受损以及核前期定位延迟,随后短暂的有丝分裂停滞。为了解决 nsPEFs 的作用靶点问题,我们利用了植物特异性的 KCH 驱动蛋白,它可以呈现两种不同的状态,具有不同的定位(靠近核或在质膜),从而驱动不同的细胞功能。我们表明,nsPEFs 会减少非转化细胞的细胞扩张,但会促进 KCH 过表达系的扩张。由于细胞伸长和细胞变宽与位于质膜上的 KCH 有关,KCH 过表达体中的反转反应为 nsPEFs 也在质膜上的直接作用提供了证据。

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