散发性肌萎缩性侧索硬化症相关运动神经元死亡中可溶性铁积累、氧化应激和胶质谷氨酸释放的意义。

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY
Neuropathology Pub Date : 2025-03-10 DOI:10.1111/neup.13033
Noriyuki Shibata, Ikuko Kataoka, Yukinori Okamura, Kumiko Murakami, Yoichiro Kato, Tomoko Yamamoto, Kenta Masui
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引用次数: 0

摘要

散发性肌萎缩性侧索硬化症(ALS)的氧化应激已被证明是通过从患者尸检中获得的大脑和脊髓运动神经元系统中核酸、脂质、糖和蛋白质的氧化修饰产物的积累。我们最近证实在散发性ALS脊髓的活化小胶质细胞中存在可溶性铁积累。这一发现可能表明,铁介导的芬顿反应最有可能是导致与该疾病相关的氧化应激的原因。散发性ALS的兴奋性氨基酸神经毒性假说是基于患者脑脊液中谷氨酸和天冬氨酸浓度的增加而提出的。最初,细胞外兴奋性氨基酸水平的增加被认为反映了上运动神经元轴突末端的过度释放。然而,受损的上运动神经元是否在疾病晚期仍能继续释放谷氨酸是一个问题。为了解决这个问题,我们假设神经胶质细胞可能是谷氨酸释放源。我们对尸体解剖的人脊髓进行免疫组化分析发现,铁蛋白、hepcidin、铁转运蛋白、乌头酶1、肿瘤坏死因子-α (TNF-α)、TNF-α转换酶(TACE)和谷氨酰胺酶c (GAC)主要在小胶质细胞中表达,胱氨酸/谷氨酸反转运蛋白(xCT)主要在星形胶质细胞中表达。接下来我们进行了细胞培养实验。可溶性铁处理的培养小胶质细胞分别通过乌头酶1和TACE过量释放谷氨酸和TNF-α。TNF-α处理的培养小胶质细胞通过GAC过度释放谷氨酸。hepcidin处理的培养小胶质细胞,其表达被TNF-α上调,显示铁转运蛋白的表达下调。培养的星形胶质细胞经过氧化氢处理过释放谷氨酸。这些观察结果在体内和体外提供了证据,证明小胶质细胞和星形胶质细胞分别是散发性ALS中可溶性铁过载和氧化应激的谷氨酸供应者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Implications for soluble iron accumulation, oxidative stress, and glial glutamate release in motor neuron death associated with sporadic amyotrophic lateral sclerosis.

Oxidative stress in sporadic amyotrophic lateral sclerosis (ALS) has been evidenced by accumulation of oxidatively modified products of nucleic acids, lipids, sugars, and proteins in the motor neuron system of brains and spinal cords obtained at autopsy from the patients. We recently demonstrated soluble iron accumulation in activated microglia of sporadic ALS spinal cords. This finding could indicate that iron-mediated Fenton reaction is most likely to be responsible for oxidative stress associated with this disease. The excitatory amino acid neurotoxicity hypothesis for sporadic ALS has been proposed based on increased glutamate and aspartate concentrations in cerebrospinal fluid from the patients. Initially, the increase in extracellular excitatory amino acid levels was considered to reflect excessive release from the axon terminal of upper motor neurons. However, it is a question of whether the damaged upper motor neurons continue releasing glutamate even in advanced stage of this disease. To address this issue, we hypothesized that glial cells might be a glutamate release source. Our immunohistochemical analysis on autopsied human spinal cords revealed that ferritin, hepcidin, ferroportin, aconitase 1, tumor necrosis factor-α (TNF-α), TNF-α-converting enzyme (TACE), and glutaminase-C (GAC) were expressed mainly in microglia and that cystine/glutamate antiporter (xCT) was expressed mainly in astrocytes. We next performed cell culture experiments. Cultured microglia treated with soluble iron over-released glutamate and TNF-α via aconitase 1 and TACE, respectively. Cultured microglia treated with TNF-α over-released glutamate via GAC. Cultured microglia treated with hepcidin, of which expression is known to be upregulated by TNF-α, showed downregulated expression of ferroportin. Cultured astrocytes treated with hydrogen peroxide over-released glutamate via xCT. These observations provide in vivo and in vitro evidence that microglia and astrocytes are glutamate suppliers in response to soluble iron overload and oxidative stress, respectively, in sporadic ALS.

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来源期刊
Neuropathology
Neuropathology 医学-病理学
CiteScore
4.10
自引率
4.30%
发文量
105
审稿时长
6-12 weeks
期刊介绍: Neuropathology is an international journal sponsored by the Japanese Society of Neuropathology and publishes peer-reviewed original papers dealing with all aspects of human and experimental neuropathology and related fields of research. The Journal aims to promote the international exchange of results and encourages authors from all countries to submit papers in the following categories: Original Articles, Case Reports, Short Communications, Occasional Reviews, Editorials and Letters to the Editor. All articles are peer-reviewed by at least two researchers expert in the field of the submitted paper.
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