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酶样纳米颗粒工程化间充质干细胞分泌 HGF 促进体内特发性肺纤维化的可视化治疗。

Enzyme-like nanoparticle-engineered mesenchymal stem cell secreting HGF promotes visualized therapy for idiopathic pulmonary fibrosis in vivo.

机构信息

Ningbo Key Laboratory of Biomedical Imaging Probe Materials and Technology, CAS Key Laboratory of Magnetic Materials and Devices, Laboratory of Advanced Theranostic Materials and Technology, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201, China.

Zhejiang International Cooperation Base of Biomedical Materials Technology and Application, Zhejiang Engineering Research Center for Biomedical Materials, Ningbo Cixi Institute of Biomedical Engineering, Cixi 315300, China.

出版信息

Sci Adv. 2024 Aug 23;10(34):eadq0703. doi: 10.1126/sciadv.adq0703. Epub 2024 Aug 21.

Abstract

Stem cell therapy is being explored as a potential treatment for idiopathic pulmonary fibrosis (IPF), but its effectiveness is hindered by factors like reactive oxygen species (ROS) and inflammation in fibrotic lungs. Moreover, the distribution, migration, and survival of transplanted stem cells are still unclear, impeding the clinical advancement of stem cell therapy. To tackle these challenges, we fabricate AuPtCoPS trimetallic-based nanocarriers (TBNCs), with enzyme-like activity and plasmid loading capabilities, aiming to efficiently eradicate ROS, facilitate delivery of therapeutic genes, and ultimately improve the therapeutic efficacy. TBNCs also function as a computed tomography contrast agent for tracking mesenchymal stem cells (MSCs) during therapy. Accordingly, we enhanced the antioxidant stress and anti-inflammatory capabilities of engineered MSCs and successfully visualized their biological behavior in IPF mice in vivo. Overall, this study provides an efficient and forward-looking treatment approach for IPF and establishes a framework for a stem cell-based therapeutic system aimed at addressing lung disease.

摘要

干细胞治疗正被探索作为特发性肺纤维化(IPF)的潜在治疗方法,但由于纤维化肺中的活性氧(ROS)和炎症等因素,其疗效受到阻碍。此外,移植干细胞的分布、迁移和存活仍不清楚,这阻碍了干细胞治疗的临床进展。为了解决这些挑战,我们制备了具有酶样活性和质粒负载能力的基于 AuPtCoPS 三金属的纳米载体(TBNCs),旨在有效清除 ROS,促进治疗基因的传递,并最终提高治疗效果。TBNCs 还可用作间充质干细胞(MSCs)治疗期间的计算机断层扫描造影剂。因此,我们增强了工程化 MSCs 的抗氧化应激和抗炎能力,并成功地在体内观察到它们在 IPF 小鼠中的生物学行为。总的来说,这项研究为 IPF 提供了一种高效且有前景的治疗方法,并为基于干细胞的治疗系统建立了一个针对肺部疾病的框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/671b/11338238/18eba38e9a93/sciadv.adq0703-f1.jpg

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