Neuron-derived extracellular vesicles enriched from plasma show altered size and miRNA cargo as a function of antidepressant drug response

小RNA 抗抑郁药 生物标志物 药理学 依西酞普兰 折叠变化 西酞普兰 神经元 生物 基因敲除 细胞生物学 胞外囊泡 内科学 内分泌学 神经科学 细胞外 医学 微泡 细胞培养 海马体 下调和上调 生物化学 基因 遗传学
作者
Saumeh Saeedi,Corina Nagy,Pascal Ibrahim,Jean‐François Théroux,Marina Wakid,Laura M. Fiori,Jennie Yang,Susan Rotzinger,Jane A. Foster,Naguib Mechawar,Sidney H. Kennedy,Gustavo Turecki
出处
期刊:Molecular Psychiatry [Springer Nature]
卷期号:26 (12): 7417-7424 被引量:101
标识
DOI:10.1038/s41380-021-01255-2
摘要

Previous work has demonstrated that microRNAs (miRNAs) change as a function of antidepressant treatment (ADT) response. However, it is unclear how representative these peripherally detected miRNA changes are to those occurring in the brain. This study aimed to use peripherally extracted neuron-derived extracellular vesicles (NDEV) to circumvent these limitations and investigate neuronal miRNA changes associated with antidepressant response. Samples were collected at two time points (baseline and after 8 weeks of follow-up) from depressed patients who responded (N = 20) and did not respond (N = 20) to escitalopram treatment, as well as controls (N = 20). Total extracellular vesicles (EVs) were extracted from plasma, and then further enriched for NDEV by immunoprecipitation with L1CAM. EVs and NDEVs were characterized, and NDEV miRNA cargo was extracted and sequenced. Subsequently, studies in cell lines and postmortem tissue were conducted. Characterization of NDEVs revealed that they were smaller than other EVs isolated from plasma (p < 0.0001), had brain-specific neuronal markers, and contained miRNAs enriched for brain functions (p < 0.0001) Furthermore, NDEVs from depressed patients were smaller than controls (p < 0.05), and NDEV size increased with ADT response (p < 0.01). Finally, changes in NDEV cargo, specifically changes in miR-21-5p, miR-30d-5p, and miR-486-5p together (p < 0.01), were associated with ADT response. Targets of these three miRNAs were altered in brain tissue from depressed individuals (p < 0.05). Together, this study indicates that changes in peripherally isolated NDEV can act as both a clinically accessible and informative biomarker of ADT response specifically through size and cargo.
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