丹皮酚通过抑制肥大细胞Src激酶磷酸化来减轻p物质诱导的荨麻疹

IF 3.7 4区 医学 Q2 CELL BIOLOGY Cellular immunology Pub Date : 2023-07-01 DOI:10.1016/j.cellimm.2023.104728
Yuanyuan Ding , Baowen Dang , Yonghui Zhang , Shiting Hu , Yuejin Wang , Chenrui Zhao , Tao Zhang , Zijun Gao
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引用次数: 1

摘要

背景慢性荨麻疹的治疗具有挑战性,急需有效的治疗药物。目的研究丹皮酚靶向肥大细胞的作用机制及其对慢性荨麻疹的治疗作用。研究设计:我们建立了体内慢性荨麻疹模型和体外肥大细胞模型,研究了丹皮酚治疗慢性荨麻疹的作用及其在肥大细胞中的作用机制。方法采用PCA和全身性过敏模型评价丹皮酚的抗过敏作用。研究了丹皮酚对荨麻疹模型的治疗作用。使用酶免疫测定试剂盒测量细胞因子和趋化因子的释放。进行蛋白质印迹分析以研究Src、PI3K和PLC的磷酸化。通过体外激酶测定研究了Lyn、PLC、PI3K和Src的激酶活性。结果在被动皮肤过敏反应模型中,丹皮酚能够减轻埃文氏蓝渗漏、血清组胺和趋化因子的释放。同时,丹皮酚抑制C57BL/6小鼠的血管舒张和肥大细胞脱颗粒。进一步研究发现,在P物质诱导的荨麻疹模型中,丹皮酚减轻了红斑和皮疹等症状,同时抑制了相关炎症因子的释放。对肥大细胞的体外验证实验发现,丹皮酚通过与Src激酶交联来抑制Src-PI3K/Lyn PLC NF-κB信号通路的激活。此外,LAD2细胞的钙内流、肥大细胞脱颗粒、细胞因子生成和趋化性降低。分子对接实验表明,丹皮酚是一种靶向Src激酶的特异性拮抗剂,可用于治疗荨麻疹等皮肤病。结论丹皮酚是一种中草药酚类化合物,可为开发治疗荨麻疹等皮肤病的新药提供候选药物。意义陈述在本研究中,我们主要研究了丹皮酚治疗慢性荨麻疹的作用及其在肥大细胞中的作用机制。有趣的是,丹皮酚被发现在肥大细胞中调节MRGPRX2触发的信号级联下游的Src激酶活性。因此,这种植物衍生的酚类化合物可能为治疗慢性荨麻疹提供一种治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Paeonol attenuates Substance P-induced urticaria by inhibiting Src kinase phosphorylation in mast cells

Background

Treatment of chronic urticaria is challenging, the discovery of effective therapeutic drugs is urgently in demand.

Purpose

To study the effect and mechanism of Paeonol targeting mast cells and its therapeutic effect on chronic urticaria.

Study design: We developed a chronic urticaria model in vivo and mast cell model in vitro examined the effect of Paeonol in the treatment of chronic urticaria and its mechanism of action in mast cells.

Method

The anti-anaphylactoid effect of Paeonol was evaluated in PCA and systemic anaphylaxis models. The treatment role of Paeonol was studied in urticaria model. The release of cytokines and chemokines was measured using enzyme immunoassay kits. Western blot analysis was conducted to investigate phosphorylation of Src, PI3K, and PLC. In vitro kinase assays were conducted to investigate the kinase activity of Lyn, PLC, PI3K and Src.

Results

In our study, Paeonol was able to attenuate evans blue leakage, serum histamine and chemokine release in a passive skin allergic reaction model. Simultaneously, Paeonol inhibited vasodilation and mast cell degranulation in C57BL/6 mice. Further research found that Paeonol alleviated symptoms such as erythema and rash in the Substance P-induced urticaria model, this is accompanied by inhibiting the release of related inflammatory factors. Validation experiments on mast cells in vitro found that Paeonol inhibited the activation of Src-PI3K/Lyn-PLC-NF-κB signaling pathway by crosslinking with Src kinase. Moreover, calcium influx, mast cell degranulation, cytokines generation and chemotaxis were reduced in LAD2 cells. Molecular docking experiments revealed that Paeonol is a specific antagonist targeting Src kinase in the treatment of skin diseases such as urticaria.

Conclusion

Paeonol, a herb-derived phenolic compound, can provide drug candidate for developing new drug in treatment of skin disease such as urticaria.

Significance statement

In this study, we primarily examined the effect of Paeonol in the treatment of chronic urticaria and its mechanism of action in mast cells. Interestingly, Paeonol was found to regulate Src kinase activity downstream of MRGPRX2 triggered signaling cascade in mast cells. Therefore, this plant-derived phenolic compound may provide a therapeutic option for the treatment of chronic urticaria.

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来源期刊
Cellular immunology
Cellular immunology 生物-免疫学
CiteScore
8.20
自引率
2.30%
发文量
102
审稿时长
30 days
期刊介绍: Cellular Immunology publishes original investigations concerned with the immunological activities of cells in experimental or clinical situations. The scope of the journal encompasses the broad area of in vitro and in vivo studies of cellular immune responses. Purely clinical descriptive studies are not considered. Research Areas include: • Antigen receptor sites • Autoimmunity • Delayed-type hypersensitivity or cellular immunity • Immunologic deficiency states and their reconstitution • Immunologic surveillance and tumor immunity • Immunomodulation • Immunotherapy • Lymphokines and cytokines • Nonantibody immunity • Parasite immunology • Resistance to intracellular microbial and viral infection • Thymus and lymphocyte immunobiology • Transplantation immunology • Tumor immunity.
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