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本文引用的文献

1
Immunostimulatory activity of Y-shaped DNA nanostructures mediated through the activation of TLR9.Y 型 DNA 纳米结构通过激活 TLR9 介导的免疫刺激活性。
Biomed Pharmacother. 2019 Apr;112:108657. doi: 10.1016/j.biopha.2019.108657. Epub 2019 Feb 21.
2
New Cytokines in the Pathogenesis of Atopic Dermatitis-New Therapeutic Targets.特应性皮炎发病机制中的新型细胞因子——新的治疗靶点。
Int J Mol Sci. 2018 Oct 9;19(10):3086. doi: 10.3390/ijms19103086.
3
Anti-obesity potential of Glycyrrhiza uralensis and licochalcone A through induction of adipocyte browning.甘草和甘草查尔酮 A 通过诱导脂肪细胞棕色化发挥抗肥胖作用。
Biochem Biophys Res Commun. 2018 Sep 10;503(3):2117-2123. doi: 10.1016/j.bbrc.2018.07.168. Epub 2018 Aug 7.
4
Atopic dermatitis-like skin lesions are suppressed in fat-1 transgenic mice through the inhibition of inflammasomes.脂肪 1 转基因小鼠通过抑制炎症小体抑制特应性皮炎样皮肤损伤。
Exp Mol Med. 2018 Jun 13;50(6):1-9. doi: 10.1038/s12276-018-0104-3.
5
Toxicity of cosmetic preservatives on human ocular surface and adnexal cells.化妆品防腐剂对人眼表面和附属器细胞的毒性。
Exp Eye Res. 2018 May;170:188-197. doi: 10.1016/j.exer.2018.02.020. Epub 2018 Feb 24.
6
Potentiation of skin TSLP production by a cosmetic colorant leads to aggravation of dermatitis symptoms.化妆品着色剂增强皮肤 TSLP 的产生导致皮炎症状加重。
Chem Biol Interact. 2018 Mar 25;284:41-47. doi: 10.1016/j.cbi.2018.02.020. Epub 2018 Feb 17.
7
Secreted immunoregulatory proteins in the skin.皮肤中分泌的免疫调节蛋白。
J Dermatol Sci. 2018 Jan;89(1):3-10. doi: 10.1016/j.jdermsci.2017.10.008. Epub 2017 Oct 26.
8
Topical ROR Inverse Agonists Suppress Inflammation in Mouse Models of Atopic Dermatitis and Acute Irritant Dermatitis.局部ROR反向激动剂可抑制特应性皮炎和急性刺激性皮炎小鼠模型中的炎症反应。
J Invest Dermatol. 2017 Dec;137(12):2523-2531. doi: 10.1016/j.jid.2017.07.819. Epub 2017 Jul 31.
9
The T Cell Response to the Contact Sensitizer Paraphenylenediamine Is Characterized by a Polyclonal Diverse Repertoire of Antigen-Specific Receptors.T细胞对接触性致敏剂对苯二胺的反应以抗原特异性受体的多克隆多样化库为特征。
Front Immunol. 2017 Feb 16;8:162. doi: 10.3389/fimmu.2017.00162. eCollection 2017.
10
Para-phenylenediamine allergy: current perspectives on diagnosis and management.对苯二胺过敏:诊断与管理的当前观点
J Asthma Allergy. 2017 Jan 18;10:9-15. doi: 10.2147/JAA.S90265. eCollection 2017.

对苯二胺,一种氧化型染发剂成分,会增加胸腺基质淋巴细胞生成素和促炎细胞因子,从而引发急性皮炎。

-phenylenediamine, an oxidative hair dye ingredient, increases thymic stromal lymphopoietin and proinflammatory cytokines causing acute dermatitis.

作者信息

Lee Jae Kwon, Lee Hye Eun, Yang Gabsik, Kim Kyu-Bong, Kwack Seung Jun, Lee Joo Young

机构信息

BK21plus Team, College of Pharmacy, The Catholic University of Korea, Bucheon, 14662 Korea.

College of Pharmacy, Dankook University, Cheonan, Korea.

出版信息

Toxicol Res. 2020 Feb 21;36(4):329-336. doi: 10.1007/s43188-020-00041-6. eCollection 2020 Oct.

DOI:10.1007/s43188-020-00041-6
PMID:33005592
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7494699/
Abstract

Due to high consumption of cosmetics in modern society, people are always exposed to the risk of skin damage and complications. -phenylenediamine (P-PD), an ingredient of hair dye, has been reported to cause allergic contact dermatitis. However, the mechanism has not been well elucidated. Here, we identify that P-PD causes dermatitis by increasing thymic stromal lymphopoietin (TSLP) and inflammatory cytokines. Topical application of P-PD to mouse ear skin in consecutive 5 days resulted in dermatitis symptoms and increased ear thickness. TSLP production in skin was upregulated by P-PD treatment alone. In addition, P-PD-induced TSLP production was potentiated by MC903, which is an in vivo TSLP inducer. P-PD increased TSLP production in keratinocytes (KCMH-1 cells and phorbol 12-myristate 13-acetate-stimulated PAM212 cells). The production of proinflammatory cytokines such as IL-1β, IL-6, IFN-γ, and CCL2, was upregulated by P-PD treatment together with MC903. The results show that repeated exposure to P-PD causes acute contact dermatitis mediated by increasing the expression of TSLP and proinflammatory cytokines.

摘要

由于现代社会中化妆品的高消费量,人们总是面临皮肤损伤和并发症的风险。对苯二胺(P-PD)是染发剂的一种成分,据报道可引起过敏性接触性皮炎。然而,其机制尚未得到充分阐明。在此,我们确定P-PD通过增加胸腺基质淋巴细胞生成素(TSLP)和炎性细胞因子来引起皮炎。连续5天将P-PD局部应用于小鼠耳部皮肤会导致皮炎症状并增加耳厚度。单独的P-PD处理可上调皮肤中TSLP的产生。此外,MC903(一种体内TSLP诱导剂)可增强P-PD诱导的TSLP产生。P-PD增加了角质形成细胞(KCMH-1细胞和佛波醇12-肉豆蔻酸酯13-乙酸酯刺激的PAM212细胞)中TSLP的产生。P-PD与MC903共同处理可上调促炎细胞因子如IL-1β、IL-6、IFN-γ和CCL2的产生。结果表明,反复接触P-PD会通过增加TSLP和促炎细胞因子的表达介导急性接触性皮炎。