题名 | Macrophage biomimetic nanoparticle-targeted functional extracellular vesicle micro-RNAs revealed via multiomics analysis alleviate sepsis-induced acute lung injury |
作者 | |
通讯作者 | Meng, Ying; Li, Xu |
发表日期 | 2024-06-23
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DOI | |
发表期刊 | |
EISSN | 1477-3155
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卷号 | 22期号:1 |
摘要 | Patients who suffer from sepsis typically experience acute lung injury (ALI). Extracellular vesicles (EVs) contain miRNAs, which are potentially involved in ALI. However, strategies to screen more effective EV-miRNAs as therapeutic targets are yet to be elucidated. In this study, functional EV-miRNAs were identified based on multiomics analysis of single-cell RNA sequencing of targeted organs and serum EV (sEV) miRNA profiles in patients with sepsis. The proportions of neutrophils and macrophages were increased significantly in the lungs of mice receiving sEVs from patients with sepsis compared with healthy controls. Macrophages released more EVs than neutrophils. MiR-125a-5p delivery by sEVs to lung macrophages inhibited Tnfaip3, while miR-221-3p delivery to lung neutrophils inhibited Fos. Macrophage membrane nanoparticles (MM NPs) loaded with an miR-125a-5p inhibitor or miR-221-3p mimic attenuated the response to lipopolysaccharide (LPS)-induced ALI. Transcriptome profiling revealed that EVs derived from LPS-stimulated bone marrow-derived macrophages (BMDMs) induced oxidative stress in neutrophils. Blocking toll-like receptor, CXCR2, or TNF alpha signaling in neutrophils attenuated the oxidative stress induced by LPS-stimulated BMDM-EVs. This study presents a novel method to screen functional EV-miRNAs and highlights the pivotal role of macrophage-derived EVs in ALI. MM NPs, as delivery systems of key sEV-miRNA mimics or inhibitors, alleviated cellular responses observed in sepsis-induced ALI. This strategy can be used to reduce septic organ damage, particularly lung damage, by targeting EVs. |
关键词 | |
相关链接 | [来源记录] |
收录类别 | |
语种 | 英语
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学校署名 | 其他
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WOS研究方向 | Biotechnology & Applied Microbiology
; Science & Technology - Other Topics
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WOS类目 | Biotechnology & Applied Microbiology
; Nanoscience & Nanotechnology
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WOS记录号 | WOS:001252421300002
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出版者 | |
ESI学科分类 | BIOLOGY & BIOCHEMISTRY
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来源库 | Web of Science
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引用统计 | |
成果类型 | 期刊论文 |
条目标识符 | http://sustech.caswiz.com/handle/2SGJ60CL/787494 |
专题 | 南方科技大学第一附属医院 |
作者单位 | 1.Southern Med Univ, Nanfang Hosp, Dept Emergency Med, Guangzhou 510515, Peoples R China 2.Southern Med Univ, State Key Lab Organ Failure Res, Guangdong Prov Key Lab Viral Hepatitis Res, Guangzhou 510515, Guangdong, Peoples R China 3.Jinan Univ, Shenzhen Peoples Hosp, Dept Gastroenterol, Clin Med Coll 2, Shenzhen 518020, Guangdong, Peoples R China 4.Southern Univ Sci & Technol, Affiliated Hosp 1, Shenzhen 518020, Guangdong, Peoples R China 5.Wenzhou Med Univ, Lishui Peoples Hosp, Cent Lab, Lishui Hosp, Lishui 323000, Zhejiang, Peoples R China 6.Southern Med Univ, Nanfang Hosp, Dept Gastroenterol, Guangdong Prov Key Lab Gastroenterol, Guangzhou 510515, Guangdong, Peoples R China 7.Southern Med Univ, Sch Pharmaceut Sci, Guangdong Prov Key Lab New Drug Screening, Guangzhou 510515, Peoples R China 8.Southern Med Univ, Gen Hosp Southern Theatre Command, Dept Intens Care Unit, Guangzhou 510515, Peoples R China 9.Southern Med Univ, Nanfang Hosp, Dept Resp Dis, Guangzhou 510515, Peoples R China |
第一作者单位 | 南方科技大学第一附属医院 |
推荐引用方式 GB/T 7714 |
Wang, Guozhen,Ma, Xiaoxin,Huang, Weichang,et al. Macrophage biomimetic nanoparticle-targeted functional extracellular vesicle micro-RNAs revealed via multiomics analysis alleviate sepsis-induced acute lung injury[J]. JOURNAL OF NANOBIOTECHNOLOGY,2024,22(1).
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APA |
Wang, Guozhen.,Ma, Xiaoxin.,Huang, Weichang.,Wang, Shuanghu.,Lou, Anni.,...&Li, Xu.(2024).Macrophage biomimetic nanoparticle-targeted functional extracellular vesicle micro-RNAs revealed via multiomics analysis alleviate sepsis-induced acute lung injury.JOURNAL OF NANOBIOTECHNOLOGY,22(1).
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MLA |
Wang, Guozhen,et al."Macrophage biomimetic nanoparticle-targeted functional extracellular vesicle micro-RNAs revealed via multiomics analysis alleviate sepsis-induced acute lung injury".JOURNAL OF NANOBIOTECHNOLOGY 22.1(2024).
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