Ferroptosis: A New Pathway in the Interaction between Gut Microbiota and Multiple Sclerosis.

IF 3.1 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in bioscience (Landmark edition) Pub Date : 2025-01-06 DOI:10.31083/FBL26265
Junjie Jian, Jun Wei
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Abstract

Multiple sclerosis (MS) is a chronic autoimmune disorder marked by neuroinflammation, demyelination, and neuronal damage. Recent advancements highlight a novel interaction between iron-dependent cell death, known as ferroptosis, and gut microbiota, which may significantly influences the pathophysiology of MS. Ferroptosis, driven by lipid peroxidation and tightly linked to iron metabolism, is a pivotal contributor to the oxidative stress observed in MS. Concurrently, the gut microbiota, known to affect systemic immunity and neurological health, emerges as an important regulator of iron homeostasis and inflammatory responses, thereby influencing ferroptotic pathways. This review investigates how gut microbiota dysbiosis and ferroptosis impact MS, emphasizing their potential as therapeutic targets. Through an integrated examination of mechanistic pathways and clinical evidence, we discuss how targeting these interactions could lead to novel interventions that not only modulate disease progression but also offer personalized treatment strategies based on gut microbiota profiling. This synthesis aims at deepening insights into the microbial contributions to ferroptosis and their implications in MS, setting the stage for future research and therapeutic exploration.

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上睑下垂:肠道菌群与多发性硬化相互作用的新途径。
多发性硬化症(MS)是一种以神经炎症、脱髓鞘和神经元损伤为特征的慢性自身免疫性疾病。最近的进展强调了铁依赖性细胞死亡(称为铁下垂)和肠道微生物群之间的一种新的相互作用,这可能显著影响ms的病理生理。铁下垂由脂质过氧化驱动,与铁代谢密切相关,是ms中观察到的氧化应激的关键因素。作为铁稳态和炎症反应的重要调节因子,从而影响铁的凋亡途径。本文综述了肠道菌群失调和铁下垂如何影响MS,强调了它们作为治疗靶点的潜力。通过对机制途径和临床证据的综合研究,我们讨论了如何靶向这些相互作用可以导致新的干预措施,不仅可以调节疾病进展,还可以提供基于肠道微生物群分析的个性化治疗策略。这项综合研究旨在深入了解微生物对铁下垂的贡献及其在MS中的意义,为未来的研究和治疗探索奠定基础。
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