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鱼类辐射状胶质细胞在低氧应激下的线粒体弹性机制。

Mechanisms of mitochondrial resilience in teleostean radial glia under hypoxic stress.

机构信息

Huizhou University, Huizhou 510607, China.

Department of Physiological Sciences and Center for Environmental and Human Toxicology, University of Florida Genetics Institute, Interdisciplinary Program in Biomedical Sciences Neuroscience, College of Veterinary Medicine, University of Florida, Gainesville, FL 32611, USA.

出版信息

Comp Biochem Physiol C Toxicol Pharmacol. 2024 Nov;285:110001. doi: 10.1016/j.cbpc.2024.110001. Epub 2024 Aug 14.

DOI:10.1016/j.cbpc.2024.110001
PMID:39151815
Abstract

Radial glial cells (RGCs) are remarkable cells, essential for normal development of the vertebrate central nervous system. In teleost fishes, RGCs play a pivotal role in neurogenesis and regeneration of injured neurons and glia. RGCs also exhibit resilience to environmental stressors like hypoxia via metabolic adaptations. In this study, we assessed the physiology of RGCs following varying degrees of hypoxia, with an emphasis on reactive oxygen species (ROS) generation, mitochondrial membrane potential (MMP), mitophagy, and energy metabolism. Our findings demonstrated that hypoxia significantly elevated ROS production and induced MMP depolarization in RGCs. The mitochondrial disturbances were closely associated with increased mitophagy, based on the co-localization of mitochondria and lysosomes. Key mitophagy-related genes were also up-regulated, including those of the BNIP3/NIX mediated pathway as well as the FUNDC1 mediated pathway. Such responses suggest robust cellular mechanisms are initiated to counteract mitochondrial damage due to increasing hypoxia. A significant metabolic shift from oxidative phosphorylation to glycolysis was also observed in RGCs, which may underlie an adaptive response to sustain cellular function and viability following a reduction in oxygen availability. Furthermore, hypoxia inhibited the synthesis of mitochondrial complexes subunits in RGCs, potentially related to elevated HIF-2α expression with 3 % O. Taken together, RGCs appear to exhibit complex adaptive responses to hypoxic stress, characterized by metabolic reprogramming and the activation of mitophagy pathways to mitigate mitochondrial dysfunction.

摘要

放射状胶质细胞(RGCs)是一种卓越的细胞,对于脊椎动物中枢神经系统的正常发育至关重要。在硬骨鱼类中,RGCs 在神经元和神经胶质的神经发生和再生中起着关键作用。RGCs 还通过代谢适应对缺氧等环境胁迫表现出弹性。在这项研究中,我们评估了 RGCs 在不同程度缺氧后的生理学变化,重点关注活性氧(ROS)生成、线粒体膜电位(MMP)、线粒体自噬和能量代谢。我们的研究结果表明,缺氧显著增加了 RGCs 中的 ROS 生成并诱导了 MMP 去极化。线粒体紊乱与线粒体自噬的增加密切相关,这是基于线粒体和溶酶体的共定位。关键的线粒体自噬相关基因也被上调,包括 BNIP3/NIX 介导途径和 FUNDC1 介导途径的基因。这些反应表明,由于缺氧增加,细胞启动了强大的机制来对抗线粒体损伤。RGCs 中还观察到从氧化磷酸化到糖酵解的显著代谢转变,这可能是对氧气供应减少时维持细胞功能和存活的适应性反应。此外,缺氧抑制了 RGCs 中线粒体复合物亚基的合成,这可能与 3% O 时 HIF-2α 表达的升高有关。综上所述,RGCs 似乎对缺氧应激表现出复杂的适应性反应,其特征是代谢重编程和激活线粒体自噬途径以减轻线粒体功能障碍。

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