{"title":"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。","authors":"Linna Zhang, , , Xianliang Yan, , , Xinzhu Li, , , Yingying Huang, , , Xiaowan Wang, , , Jiancheng Lin, , , Han Zhang*, , , Zhuang Liu*, , and , Qiang Guo*, ","doi":"10.1021/acsnano.5c07062","DOIUrl":null,"url":null,"abstract":"<p >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 H<sub>2</sub>O<sub>2</sub> 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.</p>","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":"19 37","pages":"33184–33201"},"PeriodicalIF":16.0000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Inhalation of Mesenchymal-Stem-Cell-Derived Nanovesicles Delivering Catalase Enhances the Treatment for Acute Lung Injury\",\"authors\":\"Linna Zhang, , , Xianliang Yan, , , Xinzhu Li, , , Yingying Huang, , , Xiaowan Wang, , , Jiancheng Lin, , , Han Zhang*, , , Zhuang Liu*, , and , Qiang Guo*, \",\"doi\":\"10.1021/acsnano.5c07062\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >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 H<sub>2</sub>O<sub>2</sub> 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.</p>\",\"PeriodicalId\":21,\"journal\":{\"name\":\"ACS Nano\",\"volume\":\"19 37\",\"pages\":\"33184–33201\"},\"PeriodicalIF\":16.0000,\"publicationDate\":\"2025-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Nano\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsnano.5c07062\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsnano.5c07062","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
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.
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.