Anti-Inflammatory Artificial Extracellular Vesicles with Notable Inhibition of Particulate Matter-Induced Skin Inflammation and Barrier Function Impairment

被引:7
作者
Park, Simon [1 ]
Lim, Jaesung [2 ]
Kim, Seulgi [1 ]
Jeon, Minha [1 ]
Baek, Hwira [1 ]
Park, Wooram [3 ]
Park, Juwon [4 ]
Kim, Se-Na [5 ,6 ]
Kang, Nae-Gyu [7 ]
Park, Chun Gwon [2 ,8 ]
Kim, Jin Woong [1 ]
机构
[1] Sungkyunkwan Univ, Sch Chem Engn, Suwon 16419, South Korea
[2] Sungkyunkwan Univ, SKKU Inst Convergence, Dept Intelligent Precis Healthcare Convergence, Suwon 16419, South Korea
[3] Sungkyunkwan Univ, Coll Biotechnol & Bioengn, Dept Integrat Biotechnol, Suwon 16419, South Korea
[4] Univ Hawaii Manoa, John A Burns Sch Med, Dept Trop Med Med Microbiol & Pharmacol, Honolulu, HI 96813 USA
[5] MediArk Inc, Res & Dev Ctr, Cheongju 28644, South Korea
[6] Chungbuk Natl Univ, Coll Biohlth Univ Syst, Dept Ind Cosmet Sci, Cheongju 28644, South Korea
[7] LG Household & Hlth Care, R&D Campus, Seoul 07795, South Korea
[8] Sungkyunkwan Univ, SKKU Inst Convergence, Dept Biomed Engn, Suwon 16419, South Korea
基金
新加坡国家研究基金会;
关键词
particulate matter; biosurfactant; extracellularvesicles; anti-inflammation; skin barrier function; AIR-POLLUTION; ACTIVATION; PROLIFERATION; PATHWAYS; EXOSOMES; PROMOTES; DELIVERY; DAMAGE;
D O I
10.1021/acsami.3c14377
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Particulate matter (PM) exposure disrupts the skin barrier, causing cutaneous inflammation that may eventually contribute to the development of various skin diseases. Herein, we introduce anti-inflammatory artificial extracellular vesicles (AEVs) fabricated through cell extrusion using the biosurfactant PEGylated mannosylerythritol lipid (P-MEL), hereafter named AEVP-MEL. The P-MEL has anti-inflammatory abilities with demonstrated efficacy in inhibiting the secretion of pro-inflammatory mediators. Mechanistically, AEVP-MEL enhanced anti-inflammatory response by inhibiting the mitogen-activated protein kinase (MAPK) pathway and decreasing the release of inflammatory mediators such as reactive oxygen species (ROS), cyclooxygenase-2 (COX-2), and pro-inflammatory cytokines in human keratinocytes. Moreover, AEVP-MEL promoted increased expression levels of skin barrier proteins (e.g., involucrin, IVL) and water-proteins (e.g., aquaporin 3, AQP3). In vivo studies revealed that repeated PM exposure to intact skin resulted in cutaneous inflammatory responses, including increased skin thickness (hyperkeratosis) and mast cell infiltration. Importantly, our data showed that the AEVP-MEL treatment significantly restored immune homeostasis in the skin affected by PM-induced inflammation and enhanced the intrinsic skin barrier function. This study highlights the potential of the AEVP-MEL in promoting skin health against PM exposure and its promising implications for the prevention and treatment of PM-related skin disorders.
引用
收藏
页码:59199 / 59208
页数:10
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