Scholarlink

<p>Extracellular vesicles (EVs) are emerging as promising circulating biomarkers for liquid biopsy due to their abundant molecular information, such as proteins, nucleic acids, and metabolites. However, the metabolic profiling of EVs remains largely unexplored, much less exploiting their intrinsic metabolic features for disease diagnosis. In this study, we demonstrate that the metabolic-related inducible nitric oxide synthase (iNOS) activity of macrophage-derived EVs serves as an effective biomarker for phenotypic profiling and further evaluating lung inflammation. By integrating a cascade amplification strategy that combines the biocatalysis of EV iNOS activity with the electrocatalysis of defective tungsten disulfide quantum dots (WS<sub>2</sub> QDs), we develop an ACTIVITY (Amplified Cascade-catalysis TestIng for VesIcular meTabolic activitY) method for rapid assaying of metabolically active EVs. When applied to bronchoalveolar lavage fluid samples, this activity-based EV profiling differentiates pneumonia patients from healthy controls and further facilitates the monitoring of disease treatment, suggesting the potential of EV metabolic activity for diagnostics.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Amplifying metabolic profiling of extracellular vesicle dynamics with ACTIVITY

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年3月26日

查看全文
  • Ru-Jia Yu,
  • Wei-Yi Ma,
  • Han-Yang Xiao,
  • Ya-Wei Zhang,
  • Wen-Bin Gong,
  • Zhen-Fei Yu,
  • Kai-Liang Wei,
  • Kuo-Ran Xing,
  • Xu Wang,
  • Hou-Juan Zhu,
  • Lian-Hui Wang,
  • Xian-Guang Ding

摘要

Extracellular vesicles (EVs) are emerging as promising circulating biomarkers for liquid biopsy due to their abundant molecular information, such as proteins, nucleic acids, and metabolites. However, the metabolic profiling of EVs remains largely unexplored, much less exploiting their intrinsic metabolic features for disease diagnosis. In this study, we demonstrate that the metabolic-related inducible nitric oxide synthase (iNOS) activity of macrophage-derived EVs serves as an effective biomarker for phenotypic profiling and further evaluating lung inflammation. By integrating a cascade amplification strategy that combines the biocatalysis of EV iNOS activity with the electrocatalysis of defective tungsten disulfide quantum dots (WS2 QDs), we develop an ACTIVITY (Amplified Cascade-catalysis TestIng for VesIcular meTabolic activitY) method for rapid assaying of metabolically active EVs. When applied to bronchoalveolar lavage fluid samples, this activity-based EV profiling differentiates pneumonia patients from healthy controls and further facilitates the monitoring of disease treatment, suggesting the potential of EV metabolic activity for diagnostics.