Cold resistance of mammalian hibernators ∼ a matter of ferroptosis?

Masamitsu Sone, Y. Yamaguchi
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Abstract

Most mammals adapt thermal physiology around 37°C and large deviations from their range, as observed in severe hypothermia and hyperthermia, resulting in organ dysfunction and individual death. A prominent exception is mammalian hibernation. Mammalian hibernators resist the long-term duration of severe low body temperature that is lethal to non-hibernators, including humans and mice. This cold resistance is supported, at least in part, by intrinsic cellular properties, since primary or immortalized cells from several hibernator species can survive longer than those from non-hibernators when cultured at cold temperatures. Recent studies have suggested that cold-induced cell death fulfills the hallmarks of ferroptosis, a type of necrotic cell death that accompanies extensive lipid peroxidation by iron-ion-mediated reactions. In this review, we summarize the current knowledge of cold resistance of mammalian hibernators at the cellular and molecular levels to organ and systemic levels and discuss key pathways that confer cold resistance in mammals.
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哺乳动物冬眠者的耐寒性∼与铁变态反应有关?
大多数哺乳动物的热生理学适应温度在 37°C 左右,严重偏离其范围会导致器官功能障碍和个体死亡,如严重低温症和高热症。哺乳动物的冬眠是一个突出的例外。哺乳动物冬眠能抵御长期的严重低体温,而这种低体温对非冬眠者(包括人类和小鼠)来说是致命的。这种耐寒性至少部分是由细胞的内在特性支持的,因为在低温条件下培养来自几种冬眠动物的原代细胞或永生细胞时,它们的存活时间比非冬眠动物的细胞更长。最近的研究表明,低温诱导的细胞死亡符合铁变态反应的特征,铁变态反应是一种坏死性细胞死亡,伴随着铁离子介导的广泛脂质过氧化反应。在这篇综述中,我们总结了目前从细胞和分子水平到器官和系统水平对哺乳动物冬眠者耐寒性的认识,并讨论了赋予哺乳动物耐寒性的关键途径。
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