首页|二酰甘油通过诱导中性粒细胞胞外捕获网抑制牙龈上皮角化屏障

二酰甘油通过诱导中性粒细胞胞外捕获网抑制牙龈上皮角化屏障

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目的:探讨二酰甘油(DG)诱导中性粒细胞胞外捕获网(NETs)生成和潜在的调控机制,评估NETs对牙龈上皮角化屏障的影响.方法:从MTBLS4684 数据库中获取牙周炎和健康受试者的脂质组学数据,对其进行标准化处理,分析两组中DG的含量差异.使用DG处理人外周血多形核中性粒细胞(PMNs)后,通过Western blot检测瓜氨酸化组蛋白H3(CitH3)表达,Sytox green染色检测胞外核酸变化,免疫荧光检测CitH3 表达及分布的变化.使用蛋白激酶C(PKC)抑制剂预处理PMNs后,再加入DG 刺激,通过 Western blot、Sytox green 染色和免疫荧光检测 NETs 形成.提取 NETs 刺激人牙龈角质形成细胞(HGKs),采用实时荧光定量PCR和Western blot检测兜甲蛋白(LOR)和紧密连接蛋白 2(CLDN2)的表达变化.通过免疫组化检测健康和牙周炎组牙龈上皮中LOR和CLDN2 的表达,并使用Western blot检测牙龈上皮中NETs标志物CitH3 和髓过氧化物酶(MPO)蛋白表达.结果:牙周炎患者牙龈上皮中多种 DG 含量增高.DG 刺激 PMNs 后,CitH3 蛋白表达增加(P<0.01),核酸释放到细胞外,CitH3 荧光表达增强并向细胞外分布;使用PKC抑制剂后,上述过程被有效抑制.NETs刺激HGKs细胞后,角化标志物LOR和屏障标志物CLDN2 基因和蛋白表达降低(P<0.05).牙周炎患者牙龈上皮中LOR和CLDN2表达降低,CitH3 和MPO蛋白表达增加(P<0.05).结论:DG通过激活PMNs中的PKC促进NETs形成和累积,进而破坏牙龈上皮的角化和屏障功能.
Diacylglycerol suppresses gingival epithelial keratinization and barrier by inducing neutrophil extracellular traps formation
Objective:To investigate the formation and potential regulatory mechanisms of diacylglycerol(DG)-induced neutrophil extracellular traps(NETs),and to assess the effect of NETs on the gingival epithelial keratinization and barrier.Methods:Lipidomics data from periodontitis and healthy subjects were obtained from the MTBLS4684 database,normalized and analyzed for differences of DG content between the two groups.Human peripheral blood-derived polymorphonuclear neutrophils(PMNs)were treated with DG,followed by detection of citrullinated histone H3(CitH3)expression by Western blot,extracellular nucleic acid changes by Sytox green staining,and changes of CitH3 expression and distribution by immunofluorescence.After pretreatment of PMNs with protein kinase C(PKC)inhibitor and then stimulated with DG,NETs formation was detected by Western blot,Sytox green staining and immunofluores-cence.Human gingival keratinocytes(HGKs)were stimulated by extracted NETs,and changes in the expression of loricrin(LOR)and claudin-2(CLDN2)were examined by qRT-PCR and Western blot.The levels of LOR and CLDN2 expression in the gingival epi-thelium of the healthy and periodontitis groups were detected by immunohistochemistry,and the markers of NETs,CitH3 and myeloper-oxidase(MPO),in epithelium were assayed by Western blot.Results:Multiple DG was raised in the gingival epithelium of patients with periodontitis.After stimulation of PMNs by DG,CitH3 protein expression was enhanced(P<0.01),nucleic acids were released into the extracellular zone,and CitH3 fluorescence expression was elevated with its distribution to the extracellular region;the above processes were effectively blocked by the application of PKC inhibitor.After stimulation of HGKs by NETs,the expressions of LOR and CLDN2 were decreased at the transcriptional and protein levels(P<0.05).In the periodontitis group,the levels of LOR and CLDN2 were reduced,and the expressions of CitH3 and MPO were increased in the gingival epithelium(P<0.05).Conclusions:DG promotes the formation and accumulation of NETs by activating PKC in PMNs,which in turn exerts a destructive effect on keratinization and bar-rier of epithelium.

periodontitisneutrophil extracellular trapsdiacylglycerolprotein kinase Ckeratinization barrier

崔雅云、周敏、章燕

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同济大学附属口腔医院牙周科,同济大学口腔医学院,上海牙组织修复与再生工程技术研究中心,同济大学口腔医学研究所,上海 200072

牙周炎 中性粒细胞胞外捕获网 二酰甘油 蛋白激酶C 角化屏障

国家自然科学基金项目同济大学自主原创基础研究项目

8190101322120220619

2024

口腔生物医学
南京医科大学

口腔生物医学

CSTPCD
影响因子:0.423
ISSN:1674-8603
年,卷(期):2024.15(4)
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