4.5 Article

Exosome-associated mitochondrial DNA from patients with myalgic encephalomyelitis/chronic fatigue syndrome stimulates human microglia to release IL-1β

期刊

EUROPEAN JOURNAL OF NEUROSCIENCE
卷 56, 期 10, 页码 5784-5794

出版社

WILEY
DOI: 10.1111/ejn.15828

关键词

allergies; cytokines; exosomes; extracellular vesicles; inflammation; mitochondrial DNA; myalgic encephalomyelitis; chronic fatigue syndrome; neuropeptides

资金

  1. ME/CFS Initiative Ramsay Award

向作者/读者索取更多资源

This study found that mitochondrial DNA (mtDNA) associated with serum exosomes is increased in ME/CFS patients only after exercise. Moreover, exosomes isolated from ME/CFS patients stimulate significant release of IL-1 beta from cultured human microglia, indicating that activation of microglia by serum-derived exosomes may serve as a potential novel pathogenetic factor and target for treatment of ME/CFS.
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a debilitating disease that presents with fatigue, sleep disturbances, malaise, and cognitive problems. The pathogenesis of ME/CFS is presently unknown, and serum levels of potential biomarkers have been inconsistent. Here, we show that mitochondrial DNA (mtDNA) associated with serum exosomes, is increased in ME/CFS patients only after exercise. Moreover, exosomes isolated from patients with ME/CFS stimulate significant release of IL-1 beta from cultured human microglia. These results provide evidence that activation of microglia by serum-derived exosomes may serve as a potential novel pathogenetic factor and target for treatment of ME/CFS.

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