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免疫组织化学检测苔藓样糠疹中瞬时受体电位 melastatin 2、谷胱甘肽过氧化物酶 4 和 spexin 的免疫反应性。

Immunohistochemical examination of immunoreactivity of transient receptor potential melastatin 2, glutathione peroxidase 4 and spexin in lichen planus.

机构信息

Department of Dermatology, Firat University Hospital, Elazig, Turkey.

Department of Dermatology. TR23119, Firat University Faculty of Medicine, Elazig, Turkey.

出版信息

Arch Dermatol Res. 2024 Oct 14;316(10):675. doi: 10.1007/s00403-024-03417-y.

DOI:10.1007/s00403-024-03417-y
PMID:39400728
Abstract

BACKROUND

In this study, we aimed to investigate the potential contributions to the disease by examining the immunoreactivities of SPX in LP-affected skin tissue using immunohistochemical methods, in light of its recent prominence as a molecule related to diabetes mellitus, along with apoptosis and ferroptosis mediated by GPX4 and TRPM2 channels facilitating oxidative stress-induced cell death.

OBJECTIVE

This research explored the immunohistochemical expressions of TRPM2, GPX4, and SPX in Lichen Planus (LP) patients compared to healthy individuals.

MATERIALS AND METHODS

Forty skin samples were collected, split equally between LP patients and healthy controls, excluding those with other conditions. Samples underwent immunohistochemical staining for TRPM2, SPX, and GPX4, using secondary antibodies and chromogens AEC or DAB. Histoscores were calculated based on staining diffusiveness and severity. Statistical analyses were performed with SPSS 22.0, using t-tests and ANOVA, with significance set at p < 0.05.

RESULTS

There were no demographic differences between groups (p > 0.05). LP patients showed significantly lower TRPM2 and GPX4 histoscores and higher SPX histoscores compared to controls (TRPM2 and GPX4: p < 0.001, SPX: p < 0.001). Gender and age did not affect histoscores significantly.

CONCLUSIONS

Findings suggest TRPM2, GPX4, and SPX play roles in LP pathogenesis, indicating a need for further molecular studies to clarify their involvement. This contributes to understanding LP beyond the traditional apoptosis perspective.

摘要

背景

在这项研究中,我们旨在通过使用免疫组织化学方法检查 LP 影响皮肤组织中 SPX 的免疫反应性,来研究其作为与糖尿病相关的分子的潜在贡献,同时还研究了 GPX4 和 TRPM2 通道介导的细胞凋亡和铁死亡,以促进氧化应激诱导的细胞死亡。

目的

本研究探讨了与健康个体相比,TRPM2、GPX4 和 SPX 在扁平苔藓(LP)患者中的免疫组织化学表达。

材料和方法

收集了 40 个皮肤样本,平均分为 LP 患者和健康对照组,排除了其他疾病的患者。对样本进行了 TRPM2、SPX 和 GPX4 的免疫组织化学染色,使用了二级抗体和 AEC 或 DAB 显色剂。根据染色扩散度和严重程度计算了组织评分。使用 SPSS 22.0 进行了统计分析,采用了 t 检验和 ANOVA,显著性水平设为 p<0.05。

结果

两组之间在人口统计学方面没有差异(p>0.05)。与对照组相比,LP 患者的 TRPM2 和 GPX4 组织评分显著降低,而 SPX 组织评分显著升高(TRPM2 和 GPX4:p<0.001,SPX:p<0.001)。性别和年龄对组织评分没有显著影响。

结论

研究结果表明,TRPM2、GPX4 和 SPX 在 LP 发病机制中发挥作用,表明需要进一步进行分子研究以阐明其参与的情况。这有助于超越传统的细胞凋亡视角来理解 LP。

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本文引用的文献

1
Ferroptosis: Mechanism and connections with cutaneous diseases.铁死亡:机制及其与皮肤疾病的关联
Front Cell Dev Biol. 2023 Jan 4;10:1079548. doi: 10.3389/fcell.2022.1079548. eCollection 2022.
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Mechanisms and inhibitors of ferroptosis in psoriasis.银屑病中铁死亡的机制与抑制剂
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Inhibition of keratinocyte ferroptosis suppresses psoriatic inflammation.抑制角质形成细胞铁死亡可抑制银屑病炎症。
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30-Day spexin treatment of mice with diet-induced obesity (DIO) and type 2 diabetes (T2DM) increases insulin sensitivity, improves liver functions and metabolic status.30 天的 spexin 治疗可增加饮食诱导肥胖(DIO)和 2 型糖尿病(T2DM)小鼠的胰岛素敏感性,改善肝功能和代谢状态。
Mol Cell Endocrinol. 2021 Oct 1;536:111420. doi: 10.1016/j.mce.2021.111420. Epub 2021 Aug 9.
5
Two Decades of Evolution of Our Understanding of the Transient Receptor Potential Melastatin 2 (TRPM2) Cation Channel.二十年来我们对瞬时受体电位褪黑素2(TRPM2)阳离子通道认识的演变
Life (Basel). 2021 Apr 27;11(5):397. doi: 10.3390/life11050397.
6
Effect of spexin on renal dysfunction in experimentally obese rats: potential mitigating mechanisms via galanin receptor-2.瘦素对实验性肥胖大鼠肾功能障碍的影响:通过甘丙肽受体-2发挥潜在的缓解作用。
Arch Physiol Biochem. 2023 Dec;129(4):933-942. doi: 10.1080/13813455.2021.1887265. Epub 2021 Feb 25.
7
The relationship between lichen planus and metabolic syndrome.扁平苔藓与代谢综合征的关系。
J Cosmet Dermatol. 2021 Aug;20(8):2635-2639. doi: 10.1111/jocd.13905. Epub 2020 Dec 28.
8
TRPM2 channel-mediated cell death: An important mechanism linking oxidative stress-inducing pathological factors to associated pathological conditions.TRPM2 通道介导的细胞死亡:将诱导氧化应激的病理因素与相关病理状况联系起来的重要机制。
Redox Biol. 2020 Oct;37:101755. doi: 10.1016/j.redox.2020.101755. Epub 2020 Oct 16.
9
Increased Serum Level and High Tissue Immunoexpression of Interleukin 17 in Cutaneous Lichen Planus: A Novel Therapeutic Target for Recalcitrant Cases?血清白细胞介素 17 水平升高及其在扁平苔藓组织中的高免疫表达:一种治疗难治性病例的新靶点?
Dis Markers. 2020 Jul 24;2020:6521274. doi: 10.1155/2020/6521274. eCollection 2020.
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Lichen Planus and Metabolic Syndrome: Is There a Relation?扁平苔藓与代谢综合征:存在关联吗?
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