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牙周炎中上调的铁蛋白通过转铁蛋白受体通过 ERK/P38 MAPK 途径促进人牙周韧带细胞中炎症细胞因子的表达。

Up-regulated ferritin in periodontitis promotes inflammatory cytokine expression in human periodontal ligament cells through transferrin receptor via ERK/P38 MAPK pathways.

机构信息

Department of Periodontology, Peking University School and Hospital of Stomatology, 22 Zhongguancun South Avenue, Haidian District, Beijing 100081, P.R. China.

National Clinical Research Center for Oral Diseases, Peking University School and Hospital of Stomatology, 22 Zhongguancun South Avenue, Haidian District, Beijing 100081, P.R. China.

出版信息

Clin Sci (Lond). 2019 Jan 11;133(1):135-148. doi: 10.1042/CS20180679. Print 2019 Jan 15.

Abstract

OBJECTIVE

Ferritin, an iron-binding protein, is ubiquitous and highly conserved; it plays a crucial role in inflammation, which is the main symptom of periodontitis. Full-length cDNA library analyses have demonstrated abundant expression of ferritin in human periodontal ligament. The aims of the present study were to explore how ferritin is regulated by local inflammation, and to investigate its functions and mechanisms of action in the process of periodontitis.

METHODS

Human gingival tissues were collected from periodontitis patients and healthy individuals. Experimental periodontitis was induced by ligature of second molars in mice. The expression of ferritin light polypeptide (FTL) and ferritin heavy polypeptide (FTH) were assessed by immunohistochemistry. Meanwhile, after stimulating human periodontal ligament cells (HPDLCs) with -lipopolysaccharide (LPS), interleukin (IL)-6, and tumor necrosis factor-α (TNF-α), the expression of FTH and FTL were measured. Then, IL-6 and IL-8 were measured after incubation with different concentrations of apoferritin (iron-free ferritin) and several intracellular signaling pathway inhibitors, or after knockdown of the transferrin receptor.

RESULTS

Both FTH and FTL were substantially higher in inflamed periodontal tissues than in healthy tissues. The location of the elevated expression correlated well with the extent of inflammatory infiltration. Moreover, expression of FTH and FTL were enhanced after stimulation with -LPS, IL-6, TNF-α. Apoferritin induced the production of IL-6 and IL-8 in a dose-dependent manner partly through binding to the transferrin receptor and activating ERK/P38 signaling pathways in HPDLCs.

CONCLUSIONS

Ferritin is up-regulated by inflammation and exhibits cytokine-like activity in HPDLCs inducing a signaling cascade that promotes expression of pro-inflammatory cytokines associated with periodontitis.

摘要

目的

铁蛋白是一种含铁的结合蛋白,它广泛存在且高度保守,在炎症中起着关键作用,而炎症是牙周炎的主要症状。全长 cDNA 文库分析表明,铁蛋白在人牙周韧带中大量表达。本研究旨在探讨铁蛋白如何受局部炎症调控,并研究其在牙周炎过程中的功能和作用机制。

方法

收集牙周炎患者和健康个体的人牙龈组织。通过结扎第二磨牙在小鼠中诱导实验性牙周炎。通过免疫组织化学评估铁蛋白轻链(FTL)和铁蛋白重链(FTH)的表达。同时,用脂多糖(LPS)、白细胞介素(IL)-6 和肿瘤坏死因子-α(TNF-α)刺激人牙周膜细胞(HPDLCs)后,测量 FTH 和 FTL 的表达。然后,在孵育不同浓度的脱铁蛋白(无铁铁蛋白)和几种细胞内信号通路抑制剂,或转铁蛋白受体敲低后,测量 IL-6 和 IL-8。

结果

在炎症性牙周组织中,FTH 和 FTL 的表达均明显高于健康组织。表达升高的位置与炎症浸润的程度密切相关。此外,刺激β-LPS、IL-6、TNF-α后,FTH 和 FTL 的表达增强。脱铁蛋白以剂量依赖的方式诱导 IL-6 和 IL-8 的产生,部分通过与转铁蛋白受体结合并激活 HPDLCs 中的 ERK/P38 信号通路。

结论

铁蛋白受炎症上调,并在 HPDLCs 中表现出细胞因子样活性,诱导信号级联反应,促进与牙周炎相关的促炎细胞因子的表达。

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