A fibrin gel-loaded Gouqi-derived nanovesicle (GqDNV) repairs the heart after myocardial infarction by inhibiting p38 MAPK/NF-κB p65 pathway

p38丝裂原活化蛋白激酶 心肌梗塞 纤维蛋白 NF-κB 心脏病学 医学 MAPK/ERK通路 化学 内科学 细胞生物学 免疫学 信号转导 生物 炎症
作者
Huanhuan Zhou,Xiaolei Zhou,Jianqiu Pei,Shiyin Xu,Bi-Hui Jin,Jiuling Chen,Zixuan Zhang,Mingmeng Tang,Yan Liu,Andreas K. Nüssler,Liegang Liu,Qin Xu,Wang An-xin,Min Xia,Wei Yang
出处
期刊:Journal of Nanobiotechnology [BioMed Central]
卷期号:23 (1): 535-535 被引量:5
标识
DOI:10.1186/s12951-025-03615-4
摘要

The restoration of cardiac function post-myocardial infarction (MI) remains a significant clinical challenge. Emerging evidence indicates that Goji berries ("Gouqi" in Chinese) and their extracts exhibit substantial cardioprotective properties. Here, we introduce fibrin gel-loaded Gouqi-derived nanovesicles (GqDNVs-gel) as a delivery system targeted at the infarcted myocardium. The application of GqDNVs-gel resulted in a marked improvement in survival rates over a 14-day period post-MI, enhanced cardiac function, reduced infarct size, myocardial apoptosis, and excessive fibrosis, and facilitated endogenous repair. Through a combination of transcriptomics and proteomics analyses, alongside in vitro and in vivo experiments, we identified that the cardioprotective effect of GqDNVs are mediated through the inhibition of the p38 MAPK-NF-κB p65 signaling pathway. Furthermore, GqDNVs contain abundant bioactive compounds, including proteins, genetic materials, lipids, polysaccharides, and flavonoids. GqDNVs-gel intervention can reshape the post-MI cardiac environment and modulate myocardial lipid metabolism, specifically impacting glycerophospholipid and α-linolenic acid metabolic pathways. The upregulation of the peptide Arg-Thr-Ile-Glu and the downregulation of phosphatidylethanolamine in the hearts of MI mice after GqDNVs-gel intervention may play crucial roles in modulating the associated metabolic pathways. This study is the first to highlight the multifaceted therapeutic effects of GqDNVs-gel, offering a promising strategy for enhancing cardiac function post-MI.
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