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植物细胞外活性氧如何到达其细胞内靶标。

How Extracellular Reactive Oxygen Species Reach Their Intracellular Targets in Plants.

机构信息

Research Institute of Basic Sciences, Seoul National University, Seoul 08826, Korea.

School of Biological Sciences, Seoul National University, Seoul 08826, Korea.

出版信息

Mol Cells. 2023 Jun 30;46(6):329-336. doi: 10.14348/molcells.2023.2158. Epub 2023 Feb 17.

Abstract

Reactive oxygen species (ROS) serve as secondary messengers that regulate various developmental and signal transduction processes, with ROS primarily generated by NADPH OXIDASEs (referred to as RESPIRATORY BURST OXIDASE HOMOLOGs [RBOHs] in plants). However, the types and locations of ROS produced by RBOHs are different from those expected to mediate intracellular signaling. RBOHs produce O rather than HO which is relatively long-lived and able to diffuse through membranes, and this production occurs outside the cell instead of in the cytoplasm, where signaling cascades occur. A widely accepted model explaining this discrepancy proposes that RBOH-produced extracellular O is converted to HO by superoxide dismutase and then imported by aquaporins to reach its cytoplasmic targets. However, this model does not explain how the specificity of ROS targeting is ensured while minimizing unnecessary damage during the bulk translocation of extracellular ROS (eROS). An increasing number of studies have provided clues about eROS action mechanisms, revealing various mechanisms for eROS perception in the apoplast, crosstalk between eROS and reactive nitrogen species, and the contribution of intracellular organelles to cytoplasmic ROS bursts. In this review, we summarize these recent advances, highlight the mechanisms underlying eROS action, and provide an overview of the routes by which eROS-induced changes reach the intracellular space.

摘要

活性氧 (ROS) 作为第二信使,调节各种发育和信号转导过程,ROS 主要由 NADPH 氧化酶 (在植物中称为呼吸爆发氧化酶同源物 [RBOH]) 产生。然而,RBOH 产生的 ROS 的类型和位置与预期介导细胞内信号转导的 ROS 不同。RBOH 产生的不是 HO,而是相对寿命较长且能够通过膜扩散的 O,这种产生发生在细胞外,而不是发生信号级联的细胞质中。一个被广泛接受的模型解释了这种差异,该模型提出,RBOH 产生的细胞外 O 通过超氧化物歧化酶转化为 HO,然后通过水通道蛋白导入以达到其细胞质靶标。然而,该模型无法解释如何在批量转运细胞外 ROS (eROS) 的过程中最小化不必要的损伤的同时确保 ROS 靶向的特异性。越来越多的研究提供了关于 eROS 作用机制的线索,揭示了质外体中 eROS 感知的各种机制、eROS 与活性氮物种之间的串扰以及细胞内细胞器对细胞质 ROS 爆发的贡献。在这篇综述中,我们总结了这些最新进展,强调了 eROS 作用的机制,并概述了 eROS 诱导的变化到达细胞内空间的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3329/10258463/dbb30c9aded4/molce-46-6-329-f1.jpg

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