Exploring the Therapeutic Potential of Extracellular Vesicles Anchored to the Sea Cucumber Extracellular Matrix for Treating Atopic Dermatitis.

IF 8.1 Q1 ENGINEERING, BIOMEDICAL
Biomaterials research Pub Date : 2025-02-21 eCollection Date: 2025-01-01 DOI:10.34133/bmr.0154
Sung-Han Jo, Seon-Hwa Kim, Su Chin Heo, Hongsik Cho, Iman Janghorban Esfahani, Sang-Hyug Park
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Abstract

Extracellular vesicles (EVs) are crucial for intercellular communication and affect various physiological and pathological processes. Although terrestrial EVs have been extensively studied, marine-derived EVs have yet to be explored. This study investigated the therapeutic potential of sea cucumbers, known for their regenerative and immune abilities. Sea cucumber extracellular matrix (ECM)-anchored EVs (SEVs) were isolated and characterized using physical and electrophoretic analyses. Morphological assessments have shown that SEVs have shape and size distributions similar to mammalian EVs. Internal cargo analysis revealed the encapsulation of diverse proteins and genetic molecules. In anti-inflammatory tests with a lipopolysaccharide (LPS)-induced macrophage model, the results have shown that SEVs can alleviate inflammation factors regarding inducible nitric oxide synthase (iNOS) protein and immune-related mRNA expression. Microarray analysis was conducted to elucidate SEV's pharmacological efficacy and anti-inflammatory mechanisms, showing that SEVs inhibit the nucleotide-binding oligomerization domain (NOD)-like receptor (NLR) signaling pathway. An in vivo study using a mouse model of atopic dermatitis (AD) induced by 2,4-dinitrochlorobenzene (DNCB) involved subcutaneous SEV administration, followed by severity scoring and histological analyses. Therapeutic efficacy analysis indicated improvements in the AD mouse models, including reduced skin thickness and mast cell numbers. These findings indicate their potential for treating AD. This study highlights the potential clinical applications of marine-derived EVs and offers important implications for future research and therapeutic developments.

探讨海参细胞外基质细胞外囊泡治疗特应性皮炎的潜力。
细胞外囊泡(EVs)在细胞间通讯中起着至关重要的作用,影响着各种生理和病理过程。尽管陆地电动汽车已被广泛研究,但海洋电动汽车尚未得到探索。这项研究调查了海参的治疗潜力,以其再生和免疫能力而闻名。对海参细胞外基质(ECM)锚定ev (sev)进行了分离,并采用物理和电泳分析对其进行了表征。形态学评估表明,sev的形状和大小分布与哺乳动物EVs相似。内部货物分析揭示了多种蛋白质和遗传分子的封装。在脂多糖(LPS)诱导的巨噬细胞模型的抗炎试验中,结果表明sev可以减轻诱导型一氧化氮合酶(iNOS)蛋白和免疫相关mRNA表达的炎症因子。通过芯片分析阐明SEV的药理功效和抗炎机制,发现SEV可抑制核苷酸结合寡聚域(NOD)样受体(NLR)信号通路。2,4-二硝基氯苯(DNCB)诱导的特应性皮炎(AD)小鼠模型的体内研究涉及皮下注射SEV,随后进行严重程度评分和组织学分析。治疗效果分析表明,AD小鼠模型得到改善,包括皮肤厚度和肥大细胞数量减少。这些发现表明了它们治疗阿尔茨海默病的潜力。该研究强调了海洋源性电动汽车的潜在临床应用,并为未来的研究和治疗发展提供了重要意义。
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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