Espinosa-Diez Cristina, Miguel Verónica, Mennerich Daniela, Kietzmann Thomas, Sánchez-Pérez Patricia, Cadenas Susana, Lamas Santiago
Department of Cell Biology and Immunology, Centro de Biología Molecular "Severo Ochoa" (CSIC-UAM), Nicolás Cabrera 1, 28049 Madrid, Spain.
Faculty of Biochemistry and Molecular Medicine, Biocenter Oulu, Aapistie 7, University of Oulu, FI-90230 Oulu, Finland.
Redox Biol. 2015 Dec;6:183-197. doi: 10.1016/j.redox.2015.07.008. Epub 2015 Jul 21.
Redox biological reactions are now accepted to bear the Janus faceted feature of promoting both physiological signaling responses and pathophysiological cues. Endogenous antioxidant molecules participate in both scenarios. This review focuses on the role of crucial cellular nucleophiles, such as glutathione, and their capacity to interact with oxidants and to establish networks with other critical enzymes such as peroxiredoxins. We discuss the importance of the Nrf2-Keap1 pathway as an example of a transcriptional antioxidant response and we summarize transcriptional routes related to redox activation. As examples of pathophysiological cellular and tissular settings where antioxidant responses are major players we highlight endoplasmic reticulum stress and ischemia reperfusion. Topologically confined redox-mediated post-translational modifications of thiols are considered important molecular mechanisms mediating many antioxidant responses, whereas redox-sensitive microRNAs have emerged as key players in the posttranscriptional regulation of redox-mediated gene expression. Understanding such mechanisms may provide the basis for antioxidant-based therapeutic interventions in redox-related diseases.
氧化还原生物反应现在被认为具有促进生理信号反应和病理生理线索的两面性特征。内源性抗氧化分子参与了这两种情况。本综述重点关注关键细胞亲核试剂(如谷胱甘肽)的作用,以及它们与氧化剂相互作用并与其他关键酶(如过氧化物酶)建立网络的能力。我们讨论了Nrf2-Keap1途径作为转录抗氧化反应示例的重要性,并总结了与氧化还原激活相关的转录途径。作为抗氧化反应起主要作用的病理生理细胞和组织环境的例子,我们重点介绍了内质网应激和缺血再灌注。拓扑受限的氧化还原介导的硫醇翻译后修饰被认为是介导许多抗氧化反应的重要分子机制,而氧化还原敏感的微小RNA已成为氧化还原介导的基因表达转录后调控的关键参与者。了解这些机制可能为氧化还原相关疾病的抗氧化治疗干预提供基础。