{"title":"线粒体是预处理的记忆。","authors":"Sarah Zerimech, Hung Nguyen, Selva Baltan","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Preconditioning is such a paradigm that a stimulus below the threshold of causing harm makes the brain stronger and resilient to subsequent injury. Preconditioning affords a vigorous tolerance to the brain against neurodegeneration. Numerous efforts have tried to identify the molecular targets involved in preconditioning-induced protective responses and interestingly many of those diverse mechanisms posit mitochondria as a master regulator of preconditioning. Therefore, in this review, we will critically discuss recent and emerging evidence for the involvement of mitochondria within the preconditioning paradigm. We will introduce the crucial targets and signaling cascades by which mitochondria exert preconditioning with a focus on white matter mitochondria and whether and how mechanisms for preconditioning differ in neurons and glial cells. In this aspect, we will evaluate the role of mitochondrial shaping proteins to establish structure-function interdependence for fusion-fission balance, motility, ATP production, Ca<sup>+2</sup>, and ROS scavenging. We will also discuss how aging impacts mitochondria and the consequences of mitochondrial aging on preconditioning mechanisms. We will concentrate on the regulation of mitochondrial DNA content and quantification specifically for its value as a biomarker to monitor disease conditions. The identification of these mitochondrial preconditioning mechanisms can be translated to potential pharmacological interventions to increase intrinsic resilience of the brain to injury and to develop novel approaches to neurodegenerative diseases. Moreover, mitochondria dynamics can be used as a memory or biomarker of preconditioning.</p>","PeriodicalId":72686,"journal":{"name":"Conditioning medicine","volume":" ","pages":"151-160"},"PeriodicalIF":0.0000,"publicationDate":"2021-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484407/pdf/nihms-1787747.pdf","citationCount":"0","resultStr":"{\"title\":\"Mitochondria as the memory of preconditioning.\",\"authors\":\"Sarah Zerimech, Hung Nguyen, Selva Baltan\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Preconditioning is such a paradigm that a stimulus below the threshold of causing harm makes the brain stronger and resilient to subsequent injury. Preconditioning affords a vigorous tolerance to the brain against neurodegeneration. Numerous efforts have tried to identify the molecular targets involved in preconditioning-induced protective responses and interestingly many of those diverse mechanisms posit mitochondria as a master regulator of preconditioning. Therefore, in this review, we will critically discuss recent and emerging evidence for the involvement of mitochondria within the preconditioning paradigm. We will introduce the crucial targets and signaling cascades by which mitochondria exert preconditioning with a focus on white matter mitochondria and whether and how mechanisms for preconditioning differ in neurons and glial cells. In this aspect, we will evaluate the role of mitochondrial shaping proteins to establish structure-function interdependence for fusion-fission balance, motility, ATP production, Ca<sup>+2</sup>, and ROS scavenging. We will also discuss how aging impacts mitochondria and the consequences of mitochondrial aging on preconditioning mechanisms. We will concentrate on the regulation of mitochondrial DNA content and quantification specifically for its value as a biomarker to monitor disease conditions. The identification of these mitochondrial preconditioning mechanisms can be translated to potential pharmacological interventions to increase intrinsic resilience of the brain to injury and to develop novel approaches to neurodegenerative diseases. 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引用次数: 0
摘要
预处理是这样一种模式,即低于造成伤害阈值的刺激会使大脑变得更强大,并对随后的伤害具有复原力。预处理能使大脑对神经变性产生强大的耐受力。许多人都试图找出参与预处理诱导的保护性反应的分子靶点,有趣的是,其中许多不同的机制都认为线粒体是预处理的主调节器。因此,在本综述中,我们将批判性地讨论线粒体参与预处理模式的最新证据。我们将以白质线粒体为重点,介绍线粒体发挥预处理作用的关键靶点和信号级联,以及神经元和神经胶质细胞的预处理机制是否不同以及如何不同。在这方面,我们将评估线粒体塑形蛋白的作用,以建立融合-裂变平衡、运动、ATP 生成、Ca+2 和 ROS 清除的结构-功能相互依存关系。我们还将讨论衰老如何影响线粒体以及线粒体衰老对预处理机制的影响。我们将专注于线粒体 DNA 含量的调节和量化,特别是其作为监测疾病状况的生物标志物的价值。对这些线粒体预处理机制的鉴定可转化为潜在的药物干预措施,以提高大脑对损伤的内在恢复能力,并开发出治疗神经退行性疾病的新方法。此外,线粒体动力学可用作预处理的记忆或生物标记。
Preconditioning is such a paradigm that a stimulus below the threshold of causing harm makes the brain stronger and resilient to subsequent injury. Preconditioning affords a vigorous tolerance to the brain against neurodegeneration. Numerous efforts have tried to identify the molecular targets involved in preconditioning-induced protective responses and interestingly many of those diverse mechanisms posit mitochondria as a master regulator of preconditioning. Therefore, in this review, we will critically discuss recent and emerging evidence for the involvement of mitochondria within the preconditioning paradigm. We will introduce the crucial targets and signaling cascades by which mitochondria exert preconditioning with a focus on white matter mitochondria and whether and how mechanisms for preconditioning differ in neurons and glial cells. In this aspect, we will evaluate the role of mitochondrial shaping proteins to establish structure-function interdependence for fusion-fission balance, motility, ATP production, Ca+2, and ROS scavenging. We will also discuss how aging impacts mitochondria and the consequences of mitochondrial aging on preconditioning mechanisms. We will concentrate on the regulation of mitochondrial DNA content and quantification specifically for its value as a biomarker to monitor disease conditions. The identification of these mitochondrial preconditioning mechanisms can be translated to potential pharmacological interventions to increase intrinsic resilience of the brain to injury and to develop novel approaches to neurodegenerative diseases. Moreover, mitochondria dynamics can be used as a memory or biomarker of preconditioning.