由于自噬通量受损,细胞外基质机械信号(dys)调节代谢氧化还原稳态。

IF 4.4 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Heloísa Gerardo, Tânia Lourenço, Júlio Torres, Manuela Ferreira, Célia Aveleira, Susana Simões, Lino Ferreira, Cláudia Cavadas, Paulo J Oliveira, José Teixeira, Mário Grãos
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引用次数: 0

摘要

背景:细胞外基质(ECM)硬度越来越被认为是细胞行为的关键调节因子,控制着细胞增殖、分化和代谢等过程。神经退行性疾病的特征是线粒体功能障碍、氧化应激、自噬受损和脑组织的进行性软化,但在这种情况下,机械线索如何影响细胞代谢的研究仍然很少。材料和方法:在本研究中,我们评估了脑适应性软ECM对人神经母细胞瘤(SH-SY5Y)和小鼠海马(HT22)细胞系以及小鼠原代神经元线粒体生物能量学、氧化还原平衡和自噬能力的长期影响。结果:我们观察到,长时间暴露于软ECM并不影响神经元细胞的增殖能力,但会导致线粒体生物能量功能障碍、氧化还原失衡和自噬通量中断。这些发现在人类和小鼠的神经细胞中都得到了一致的验证。我们的数据表明,长期暴露于软ECM的细胞最大自噬能力下降,可能是由于自噬体形成和降解的不平衡,正如氯喹诱导的自噬通量抑制后LC3 II水平下降所证明的那样。这种自噬损伤与细胞氧化应激增加相结合,进一步表明代谢改变。结论:这些发现强调了ECM硬度在调节神经元细胞代谢中的关键作用,并表明长时间暴露于软ECM可能模拟神经退行性疾病病理的关键方面,从而增强了体外模型的生理相关性。这项研究强调了进一步研究ECM机制作为神经退行性疾病进展的一个促进因素和作为治疗策略的潜在靶点的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extracellular matrix mechanical cues (dys)regulate metabolic redox homeostasis due to impaired autophagic flux.

Background: Extracellular matrix (ECM) stiffness is increasingly recognized as a critical regulator of cellular behaviour, governing processes such as proliferation, differentiation, and metabolism. Neurodegenerative diseases are characterized by mitochondrial dysfunction, oxidative stress, impaired autophagy, and progressive softening of the brain tissue, yet research into how mechanical cues influence cellular metabolism in this context remains scarce.

Materials and methods: In this study, we evaluated the long-term effects of brain-compliant, soft ECM on mitochondrial bioenergetics, redox balance, and autophagic capacity in human neuroblastoma (SH-SY5Y) and mouse hippocampal (HT22) cell lines, as well as primary mouse neurons.

Results: We observed that prolonged exposure to soft ECM does not impact cell proliferative capacity of neuronal cells but results in mitochondrial bioenergetic dysfunction, redox imbalance, and disrupted autophagic flux. These findings were consistently validated across both human and mouse neuronal cells. Our data indicate a decreased maximal autophagic capacity in cells exposed to long-term soft ECM, potentially due to an imbalance in autophagosome formation and degradation, as demonstrated by decreased LC3 II levels following chloroquine-induced autophagic flux inhibition. This impairment in autophagy was coupled with increased cellular oxidative stress, further indicating metabolic alterations.

Conclusions: These findings emphasize the critical role of ECM stiffness in regulating neuronal cell metabolism and suggest that prolonged exposure to soft ECM may mimic key aspects of neurodegenerative disease pathology, thereby enhancing the physiological relevance of in vitro models. This study underscores the necessity for further research into ECM mechanics as a contributing factor in neurodegenerative disease progression and as a potential target for therapeutic strategies.

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来源期刊
CiteScore
9.50
自引率
3.60%
发文量
192
审稿时长
1 months
期刊介绍: EJCI considers any original contribution from the most sophisticated basic molecular sciences to applied clinical and translational research and evidence-based medicine across a broad range of subspecialties. The EJCI publishes reports of high-quality research that pertain to the genetic, molecular, cellular, or physiological basis of human biology and disease, as well as research that addresses prevalence, diagnosis, course, treatment, and prevention of disease. We are primarily interested in studies directly pertinent to humans, but submission of robust in vitro and animal work is also encouraged. Interdisciplinary work and research using innovative methods and combinations of laboratory, clinical, and epidemiological methodologies and techniques is of great interest to the journal. Several categories of manuscripts (for detailed description see below) are considered: editorials, original articles (also including randomized clinical trials, systematic reviews and meta-analyses), reviews (narrative reviews), opinion articles (including debates, perspectives and commentaries); and letters to the Editor.
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