Topical Application of Nano-sized Graphene Oxide Cream Ameliorates Acute Skin Inflammation in Mice.

Hyun Jung Park, Sung Won Lee, Tae-Cheol Kim, Yun Hoo Park, Keun Soo Kim, Luc Van Kaer, Suklyun Hong, Seokmann Hong
{"title":"Topical Application of Nano-sized Graphene Oxide Cream Ameliorates Acute Skin Inflammation in Mice.","authors":"Hyun Jung Park, Sung Won Lee, Tae-Cheol Kim, Yun Hoo Park, Keun Soo Kim, Luc Van Kaer, Suklyun Hong, Seokmann Hong","doi":"10.1016/j.jid.2024.08.041","DOIUrl":null,"url":null,"abstract":"<p><p>We have previously shown that nano-sized graphene oxide (NGO) displays anti-inflammatory activities against natural killer T (NKT) cell-mediated sepsis. To address whether NGO could be applied to treat acute skin inflammation we developed a conventional skin Cetaphil® cream containing NGO (NGO cream) for topical application to skin lesions and investigated its therapeutic efficacy by employing the tape-stripping-induced acute skin inflammation model. Topical application of NGO cream to the wounded area significantly reduced skin lesions compared with the control cream. Moreover, NGO cream treatment prevented the tape-stripping-elicited infiltration of and IL1β production by skin neutrophils and dendritic cells (DCs). Furthermore, such anti-inflammatory effects of NGO cream were attributed to decreased infiltration of IL12-producing DCs and IFNγ-producing cells (e.g., CD4<sup>+</sup> T, CD8<sup>+</sup> T, γδ T, NK, and NKT cells) into the skin. In addition, topical NGO cream administration enhanced the expression of suppressive molecules such as FR4 on skin regulatory T cells. Through RNA sequencing analysis, we found that the preventive effect of NGO cream on acute skin inflammation may be correlated with the activation of keratinocytes located in the epidermis. Our results support NGO cream as a therapeutic option to control acute skin inflammation.</p>","PeriodicalId":94239,"journal":{"name":"The Journal of investigative dermatology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of investigative dermatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.jid.2024.08.041","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

We have previously shown that nano-sized graphene oxide (NGO) displays anti-inflammatory activities against natural killer T (NKT) cell-mediated sepsis. To address whether NGO could be applied to treat acute skin inflammation we developed a conventional skin Cetaphil® cream containing NGO (NGO cream) for topical application to skin lesions and investigated its therapeutic efficacy by employing the tape-stripping-induced acute skin inflammation model. Topical application of NGO cream to the wounded area significantly reduced skin lesions compared with the control cream. Moreover, NGO cream treatment prevented the tape-stripping-elicited infiltration of and IL1β production by skin neutrophils and dendritic cells (DCs). Furthermore, such anti-inflammatory effects of NGO cream were attributed to decreased infiltration of IL12-producing DCs and IFNγ-producing cells (e.g., CD4+ T, CD8+ T, γδ T, NK, and NKT cells) into the skin. In addition, topical NGO cream administration enhanced the expression of suppressive molecules such as FR4 on skin regulatory T cells. Through RNA sequencing analysis, we found that the preventive effect of NGO cream on acute skin inflammation may be correlated with the activation of keratinocytes located in the epidermis. Our results support NGO cream as a therapeutic option to control acute skin inflammation.

局部使用纳米级氧化石墨烯霜可改善小鼠急性皮肤炎症。
我们曾研究表明,纳米氧化石墨烯(NGO)对自然杀伤T细胞(NKT)介导的败血症具有抗炎活性。为了解决非政府组织是否可用于治疗急性皮肤炎症的问题,我们开发了一种含有非政府组织的传统皮肤 Cetaphil® 乳霜(非政府组织乳霜),用于局部涂抹于皮肤损伤处,并通过使用胶带绷带诱导的急性皮肤炎症模型研究了其疗效。与对照药膏相比,在受伤部位局部涂抹非政府组织药膏能明显减轻皮损。此外,NGO 药膏还能阻止胶带撕裂引起的皮肤中性粒细胞和树突状细胞(DCs)的浸润和 IL1β 的产生。此外,NGO 软膏的抗炎作用还归因于产生 IL12 的 DC 和产生 IFNγ 的细胞(如 CD4+ T、CD8+ T、γδ T、NK 和 NKT 细胞)对皮肤的浸润减少。此外,局部使用非政府组织药膏可增强皮肤调节性 T 细胞上 FR4 等抑制性分子的表达。通过 RNA 测序分析,我们发现非政府组织乳膏对急性皮肤炎症的预防作用可能与表皮角质细胞的活化有关。我们的研究结果支持将非政府组织乳膏作为控制急性皮肤炎症的一种治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信