Institute of Biochemistry and Department of Biology, Carleton University, Ottawa, Ontario, Canada.
BioMEMS Resource Center & Center for Engineering in Medicine and Surgery, Massachusetts General Hospital & Harvard Medical School, Charlestown, Massachusetts, USA.
Cell Biochem Funct. 2021 Jul;39(5):623-635. doi: 10.1002/cbf.3627. Epub 2021 Feb 24.
Mammalian hibernators undergo major behavioural, physiological and biochemical changes to survive hypothermia, ischaemia-reperfusion and finite fuel reserves during days or weeks of continuous torpor. During hibernation, the 13-lined ground squirrel (Ictidomys tridecemlineatus) undergoes a global suppression of energetically expensive processes such as transcription and translation, while selectively upregulating certain genes/proteins to mitigate torpor-related damage. Antioxidant defenses are critical for preventing damage caused by reactive oxygen species (ROS) during torpor and arousal, and Nrf2 is a critical regulator of these antioxidant genes. This study analysed the relative protein expression levels of Nrf2, KEAP1, small Mafs (MafF, MafK and MafG) and catalase and the regulation of Nrf2 transcription factors by post-translational modifications (PTMs) and protein-protein interactions with a negative regulator (KEAP1) during hibernation. It was found that a significant increase in MafK during late torpor predicated an increase in relative Nrf2 and catalase levels seen in arousal. Additionally, Nrf2-KEAP1 protein-protein interactions and Nrf2 PTMs, including serine phosphorylation and lysine acetylation, were responsive to cycles of torpor-arousal with peak responses occurring during arousal. These peaks seen during arousal correspond to a surge in oxygen consumption, which causes increased ROS production. Thus, these regulatory mechanisms could be important during hibernation because they provide mechanisms for mitigating the deleterious effects of oxidative stress by modifying Nrf2 expression and function in an energetically inexpensive manner.
哺乳动物冬眠动物为了在持续数天或数周的低温、缺血再灌注和有限的燃料储备期间生存,会经历重大的行为、生理和生化变化。在冬眠期间,十三线地松鼠(Ictidomys tridecemlineatus)经历了转录和翻译等能量消耗昂贵过程的全面抑制,同时选择性地上调某些基因/蛋白质以减轻与冬眠相关的损伤。抗氧化防御对于防止活性氧(ROS)在冬眠和觉醒期间引起的损伤至关重要,而 Nrf2 是这些抗氧化基因的关键调节剂。本研究分析了 Nrf2、KEAP1、小 Mafs(MafF、MafK 和 MafG)和过氧化氢酶的相对蛋白表达水平,以及 Nrf2 转录因子的翻译后修饰(PTMs)和与负调节剂(KEAP1)的蛋白-蛋白相互作用在冬眠期间的调节。研究发现,晚期冬眠期间 MafK 的显著增加预示着觉醒时 Nrf2 和过氧化氢酶水平的相对增加。此外,Nrf2-KEAP1 蛋白-蛋白相互作用和 Nrf2 PTMs,包括丝氨酸磷酸化和赖氨酸乙酰化,对冬眠-觉醒循环有反应,峰值出现在觉醒时。在觉醒时观察到的这些峰值与氧消耗的激增相对应,这会导致 ROS 产生增加。因此,这些调节机制在冬眠期间可能很重要,因为它们通过以能量廉价的方式修饰 Nrf2 表达和功能,为减轻氧化应激的有害影响提供了机制。