Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, KU Leuven-University of Leuven, 3000 Leuven, Belgium.
Int J Mol Sci. 2019 Jul 26;20(15):3673. doi: 10.3390/ijms20153673.
Hydrogen peroxide (HO), a non-radical reactive oxygen species generated during many (patho)physiological conditions, is currently universally recognized as an important mediator of redox-regulated processes. Depending on its spatiotemporal accumulation profile, this molecule may act as a signaling messenger or cause oxidative damage. The focus of this review is to comprehensively evaluate the evidence that peroxisomes, organelles best known for their role in cellular lipid metabolism, also serve as hubs in the HO signaling network. We first briefly introduce the basic concepts of how HO can drive cellular signaling events. Next, we outline the peroxisomal enzyme systems involved in HO metabolism in mammals and reflect on how this oxidant can permeate across the organellar membrane. In addition, we provide an up-to-date overview of molecular targets and biological processes that can be affected by changes in peroxisomal HO metabolism. Where possible, emphasis is placed on the molecular mechanisms and factors involved. From the data presented, it is clear that there are still numerous gaps in our knowledge. Therefore, gaining more insight into how peroxisomes are integrated in the cellular HO signaling network is of key importance to unravel the precise role of peroxisomal HO production and scavenging in normal and pathological conditions.
过氧化氢(HO)是在许多(病理)生理条件下产生的非自由基活性氧物质,目前被普遍认为是氧化还原调节过程的重要介质。根据其时空积累情况,该分子可以作为信号信使发挥作用,也可能导致氧化损伤。本综述的重点是全面评估证据,证明过氧化物酶体,即已知在细胞脂质代谢中起作用的细胞器,也作为 HO 信号网络的枢纽。我们首先简要介绍 HO 如何驱动细胞信号事件的基本概念。接下来,我们概述了哺乳动物中参与 HO 代谢的过氧化物酶体酶系统,并思考这种氧化剂如何穿过细胞器膜。此外,我们还提供了最新的关于分子靶标和生物学过程的概述,这些过程可以受到过氧化物酶体 HO 代谢变化的影响。在可能的情况下,重点放在所涉及的分子机制和因素上。从呈现的数据来看,我们的知识显然仍然存在许多空白。因此,深入了解过氧化物体如何整合到细胞 HO 信号网络中对于揭示过氧化物体 HO 产生和清除在正常和病理条件下的精确作用至关重要。