吸入传递过氧化氢酶的间充质干细胞来源的纳米囊泡增强急性肺损伤的治疗。

IF 16 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ACS Nano Pub Date : 2025-09-09 DOI:10.1021/acsnano.5c07062
Linna Zhang, , , Xianliang Yan, , , Xinzhu Li, , , Yingying Huang, , , Xiaowan Wang, , , Jiancheng Lin, , , Han Zhang*, , , Zhuang Liu*, , and , Qiang Guo*, 
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引用次数: 0

摘要

急性肺损伤(ALI)的特点是活性氧(ROS)过度积累,引发严重的炎症级联反应,破坏肺泡-毛细血管屏障,导致呼吸衰竭和危及生命的结局。考虑到当前治疗干预措施的局限性和副作用,制定针对ALI复杂病理生理机制的有效安全策略对于改善患者预后至关重要。在此,我们通过将过氧化氢酶(CAT)包封在间充质干细胞衍生的纳米囊泡(MSCNVs)中,开发了一种可吸入的多功能纳米治疗剂(MSCNVs@CAT)。具体来说,CAT通过有效地将H2O2分解成水和氧来清除ROS,表现出强大的抗氧化性能。同时,mscnv本身含有转化生长因子-β、白细胞介素-10、肝细胞生长因子等间充质干细胞源性因子,在临床研究中证实具有免疫调节和再生能力。MSCNVs@CAT的吸入促进了靶向肺输送,并通过抗氧化、抗炎和修复功能的协同相互作用产生了有效的治疗效果。因此,MSCNVs@CAT通过平衡促炎/抗炎免疫反应和修复肺泡-毛细血管屏障来恢复ALI中的炎症稳态。其机制主要与NF-κB和细胞-细胞连接信号通路有关。总的来说,本研究提出了治疗ALI的强效可吸入纳米疗法,在有效和安全治疗肺炎方面具有重要的转化潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Inhalation of Mesenchymal-Stem-Cell-Derived Nanovesicles Delivering Catalase Enhances the Treatment for Acute Lung Injury

Inhalation of Mesenchymal-Stem-Cell-Derived Nanovesicles Delivering Catalase Enhances the Treatment for Acute Lung Injury

Acute lung injury (ALI) is characterized by the excessive accumulation of reactive oxygen species (ROS), which triggers a severe inflammatory cascade and the destruction of the alveolar–capillary barrier, leading to respiratory failure and life-threatening outcomes. Considering the limitations and adverse effects associated with current therapeutic interventions, developing effective and safe strategies that target the complex pathophysiological mechanisms of ALI is crucial for improving patient outcomes. Herein, we developed an inhalable, multifunctional nanotherapeutic (MSCNVs@CAT) by encapsulating catalase (CAT) in mesenchymal-stem-cell-derived nanovesicles (MSCNVs). Specifically, CAT scavenged ROS by efficiently decomposing H2O2 into water and oxygen, exhibiting potent antioxidant properties. Meanwhile, MSCNVs contained inherent mesenchymal-stem-cell-derived factors, including transforming growth factor-β, interleukin-10, hepatocyte growth factor, and so on, which proved immunomodulatory and regenerative capabilities in clinical studies. Inhalation of MSCNVs@CAT facilitated targeted pulmonary delivery and elicited potent therapeutic effects by the synergistic interplay of antioxidant, anti-inflammatory, and reparative functions. Consequently, MSCNVs@CAT restored inflammatory homeostasis in ALI by balancing the pro-inflammatory/anti-inflammatory immune responses and repairing the alveolar–capillary barriers. The mechanisms are primarily associated with the NF-κB and cell–cell junction signaling pathways. Overall, this study presented potent inhalable nanotherapeutics for treating ALI, which possessed significant translational potential for the effective and safe treatment of pneumonia.

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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
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