RNA profiling of sEV (small extracellular vesicles)/exosomes reveals biomarkers and vascular endothelial dysplasia with moyamoya disease

微泡 生物 发病机制 下调和上调 核糖核酸 转录组 折叠变化 分子生物学 小RNA 细胞生物学 基因表达 免疫学 遗传学 基因
作者
Shihao He,Jianfeng Liang,Guifeng Xue,Yanru Wang,Yahui Zhao,Ziqi Liu,Xiaokuan Hao,Yanchang Wei,Xiaolin Chen,Hao Wang,Shuai Kang,Rong Wang,Yuanli Zhao,Xun Ye
出处
期刊:Journal of Cerebral Blood Flow and Metabolism [SAGE Publishing]
卷期号:43 (7): 1194-1205 被引量:6
标识
DOI:10.1177/0271678x231162184
摘要

The association of exosomal RNA profiling and pathogenesis of moyamoya disease (MMD) and intracranial Atherosclerotic disease (ICAD) is unknown. In this study, we investigated the RNA profiles of sEV (small extracellular vesicles)/exosomes in patients with MMD and ICAD. Whole blood samples were collected from 30 individuals, including 10 patients with MMD, 10 patients with ICAD, and 10 healthy individuals. Whole transcriptome analysis was performed using the GeneChip WT Pico Reagent kit. Transcriptional correlation was verified using quantitative reverse transcription-polymerase chain reaction (qRT-PCR). The association between functional dysregulation and candidate RNAs was studied in vitro. In total, 1,486 downregulated and 2,405 upregulated RNAs differed significantly between patients with MMD and healthy controls. Differential expression of six circRNAs was detected using qPCR. Among these significantly differentially expressed RNAs, IPO11 and PRMT1 circRNAs were upregulated, whereas CACNA1F circRNA was downregulated. This is the first study showing that the differential expression of exosomal RNAs associated with MMD pathogenesis, such as overexpression of IPO11 and PRMT1 circRNAs, may be related to angiogenesis in MMD. The downregulation of CACNA1F circRNA may be related to vascular occlusion. These results propose the utility of exosomal RNAs as biological markers in MMD.

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