Amniotic fluid-derived extracellular vesicles: characterization and therapeutic efficacy in an experimental model of bronchopulmonary dysplasia

Amniotic fluid-derived extracellular vesicles: characterization and therapeutic efficacy in an experimental model of bronchopulmonary dysplasia
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DOI:
10.1016/j.jcyt.2021.07.011
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发表时间:
2021-11-17
期刊:
影响因子:
4.5
通讯作者:
Mitrani, Maria Ines
Mitrani, Maria Ines
中科院分区:
医学3区
文献类型:
--
作者:
Bellio, Michael A.;Young, Karen C.;Mitrani, Maria Ines

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背景目的:细胞外囊泡(EVs)作为一种新的治疗方法正在被测试。然而,电动汽车的最佳来源目前正在调查中。羊水(AF)是ev的天然来源,可以很容易地获得用于再生医学,但AF- ev的表征尚未得到充分的探索。方法:本文作者证明AF是ev的丰富来源,并鉴定了microRNA和蛋白质组学货物。生物信息学分析揭示了多种途径靶点,包括免疫调节、抗炎和自由基清除网络。作者进一步证明了EV产品作为支气管肺发育不良(BPD)的新型预防药物的治疗潜力。结果:在实验性BPD模型中,气管内注射af - ev可保护肺泡发育,减轻血管重塑和肺动脉高压,降低肺促炎细胞因子表达,减少巨噬细胞浸润。结论:作者的研究结果表明,AF是一种可行的电动汽车生物液,AF-电动汽车对肺部疾病(如BPD)具有很强的治疗潜力,值得进一步开发,将这种新型电动汽车产品转化为临床产品。(c) 2021年国际细胞与基因治疗学会。Elsevier Inc.出版。版权所有。
Background aims: Extracellular vesicles (EVs) are being tested for their use as novel therapeutics. However, the optimal source of EVs is currently under investigation. Amniotic fluid (AF) is a natural source of EVs that can be easily obtained for use in regenerative medicine, yet AF-EV characterization has not been fully explored. Methods: Here the authors demonstrate AF as a rich source of EVs and identify the microRNA and proteomic cargo. Bioinformatics analysis of this cargo revealed multiple pathway targets, including immunomodulatory, anti-inflammatory and free radical scavenging networks. The authors further demonstrated the therapeutic potential of this EV product as a novel preventative agent for bronchopulmonary dysplasia (BPD). Results: Intra-tracheal administration of AF-EVs preserved alveolar development, attenuated vascular remodeling and pulmonary hypertension, decreased lung pro-inflammatory cytokine expression and reduced macrophage infiltration in an experimental BPD model. Conclusions: The authors' results suggest that AF is a viable biological fluid for EV harvest and that AF-EVs have strong therapeutic potential for pulmonary diseases, such as BPD, warranting further development to transition this novel EV product into the clinic. (c) 2021 International Society for Cell & Gene Therapy. Published by Elsevier Inc. All rights reserved.