金属硫蛋白-3介导的细胞内锌在完全的弗氏佐剂诱导的炎症性疼痛小鼠模型中介导抗氧化和抗炎反应。

IF 10.4 2区 生物学 Q1 CELL BIOLOGY Cell Death Discovery Pub Date : 2025-02-04 DOI:10.1038/s41420-025-02322-1
Ngoc Buu Tran, Sook-Jeong Lee
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引用次数: 0

摘要

慢性炎症性疼痛通常由外周组织损伤和持续炎症引起。这种疾病严重影响患者的身体和社会福祉。在MT3敲除小鼠后爪炎性疼痛模型中,我们研究了金属硫蛋白-3 (MT3)在调节完全弗氏佐剂(CFA)诱导的细胞内Zn2+活性中的作用。结果表明,增加细胞内Zn2+水平可以改善运动行为的缺陷,以及爪子、脾脏和胸腺的炎症。此外,在CFA诱导的MT3敲除小鼠中,细胞内Zn2+在调节氧化应激标志物(谷胱甘肽、超氧化物歧化酶、过氧化氢酶和丙二醛)和炎症细胞因子(如肿瘤坏死因子-α和白细胞介素-6)中起着至关重要的作用。这项研究强调了MT3在协调细胞内与Zn2+相互作用中的关键作用,这对免疫系统的保护功能至关重要。这些相互作用是维持体内金属离子稳态和调节各种生物分子合成的基础。
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Metallothionein-3-mediated intracellular zinc mediates antioxidant and anti-inflammatory responses in the complete Freund's adjuvant-induced inflammatory pain mouse model.

Chronic inflammatory pain is often caused by peripheral tissue damage and persistent inflammation. This disease substantially affects patients' physical and social well-being. We investigated the role of metallothionein-3 (MT3) in modulating complete Freund's adjuvant (CFA)-induced intracellular Zn2+ activity in an MT3 knockout mouse model of inflammatory pain in the hind paw. The results demonstrated that increasing intracellular Zn2+ levels ameliorate deficits in motor behavior, as well as inflammation in the paw, spleen, and thymus. Furthermore, intracellular Zn2+ was crucial in regulating oxidative stress markers (glutathione, superoxide dismutase, catalase, and malondialdehyde) and inflammatory cytokines, such as tumor necrosis factor-α and interleukin-6, in MT3 knockout mice induced with CFA. This study highlights the critical role of MT3 in coordinating the intracellular interaction with Zn2+, which is vital for the immune systems's protective functions. These interactions are fundamental for maintaining metal ion homeostasis and regulating the synthesis of various biomolecules in the body.

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来源期刊
Cell Death Discovery
Cell Death Discovery Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
8.30
自引率
1.40%
发文量
468
审稿时长
9 weeks
期刊介绍: Cell Death Discovery is a multidisciplinary, international, online-only, open access journal, dedicated to publishing research at the intersection of medicine with biochemistry, pharmacology, immunology, cell biology and cell death, provided it is scientifically sound. The unrestricted access to research findings in Cell Death Discovery will foster a dynamic and highly productive dialogue between basic scientists and clinicians, as well as researchers in industry with a focus on cancer, neurobiology and inflammation research. As an official journal of the Cell Death Differentiation Association (ADMC), Cell Death Discovery will build upon the success of Cell Death & Differentiation and Cell Death & Disease in publishing important peer-reviewed original research, timely reviews and editorial commentary. Cell Death Discovery is committed to increasing the reproducibility of research. To this end, in conjunction with its sister journals Cell Death & Differentiation and Cell Death & Disease, Cell Death Discovery provides a unique forum for scientists as well as clinicians and members of the pharmaceutical and biotechnical industry. It is committed to the rapid publication of high quality original papers that relate to these subjects, together with topical, usually solicited, reviews, editorial correspondence and occasional commentaries on controversial and scientifically informative issues.
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