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源自脐带间充质干细胞的挤出纳米囊泡无致瘤潜力。

Extruded nanovesicles derived from umbilical cord mesenchymal stem cells exhibit No tumorigenic potential.

作者信息

Wang Fei, Li Lanya, Deng Junyao, Mo Shushan, Ai Jiacong, Xiao Yingxian, Li Qishan, Ding Dandan, Zhang Yixin, Zhou Dongfang, Li Zhenhua

机构信息

The Tenth Affiliated Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, 523059, China.

Guangdong Provincial Key Laboratory of Cardiac Function and Microcirculation, Guangzhou, 510515, China.

出版信息

Bioact Mater. 2025 Jul 3;52:866-876. doi: 10.1016/j.bioactmat.2025.06.056. eCollection 2025 Oct.

Abstract

Mesenchymal stem cells (MSCs) and MSC-derived extracellular vesicles (MSC EVs) have gained significant attention in biomedical and therapeutic applications. Nevertheless, their translation in clinical practice remains limited due to the lack of scalable manufacturing techniques and the prevailing safety concerns. Cell-derived extruded nanovesicles (eNVs) with high production efficiency are regarded as promising substitutes of EVs. However, like MSC EVs, their potential for tumorigenicity has yet to be exhaustively investigated. In this work, we investigated the tumorigenicity of umbilical cord mesenchymal stem cell-derived eNVs (UMSC eNVs). A549 cancer cell-derived eNVs (A549 eNVs) with potential tumorigenicity were also prepared for comparative analysis. Our characterization findings revealed that, although UMSC eNVs and A549 eNVs exhibited similar morphologies, they differed in their molecular composition. Subsequent animal experiments demonstrated the low tumorigenicity risk of UMSC eNVs in inducing tumor pathogenesis and development. Furthermore, microRNAs (miRNAs) profiling analyses suggested that the reduced tumorigenicity of UMSC eNVs might be due to the downregulation of hsa-miR-21-5p_R+1 and hsa-miR-192-5p, and upregulation of hsa-miR-143-3p and hsa-miR-146a-5p compared to A549 eNVs. The present study provided direct experimental confirmation and underlying miRNA profiling evidence of the biosafety of UMSC eNVs in terms of tumorigenicity, which will promote the future advancement and translation of UMSC eNVs.

摘要

间充质干细胞(MSCs)和源自MSCs的细胞外囊泡(MSC EVs)在生物医学和治疗应用中受到了广泛关注。然而,由于缺乏可扩展的制造技术以及普遍存在的安全问题,它们在临床实践中的转化仍然有限。具有高生产效率的细胞衍生挤压纳米囊泡(eNVs)被认为是EVs的有前途的替代品。然而,与MSC EVs一样,它们的致瘤潜力尚未得到详尽研究。在这项工作中,我们研究了脐带间充质干细胞衍生的eNVs(UMSC eNVs)的致瘤性。还制备了具有潜在致瘤性的A549癌细胞衍生的eNVs(A549 eNVs)用于比较分析。我们的表征结果表明,尽管UMSC eNVs和A549 eNVs表现出相似的形态,但它们的分子组成不同。随后的动物实验证明了UMSC eNVs在诱导肿瘤发病机制和发展方面的低致瘤风险。此外,微小RNA(miRNAs)谱分析表明,与A549 eNVs相比,UMSC eNVs致瘤性降低可能是由于hsa-miR-21-5p_R+1和hsa-miR-192-5p的下调以及hsa-miR-143-3p和hsa-miR-146a-5p的上调。本研究提供了UMSC eNVs在致瘤性方面生物安全性的直接实验证实和潜在的miRNA谱证据,这将促进UMSC eNVs未来的发展和转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b112/12271084/51b8ba56d7b3/ga1.jpg

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