Retrovirus-like gag protein Arc/Arg3.1 is involved in extracellular-vesicle-mediated mRNA transfer between glioma cells

胶质瘤 弧(几何) 细胞生物学 谷氨酸的 信使核糖核酸 突触可塑性 生物 化学 谷氨酸受体 癌症研究 生物化学 受体 几何学 数学 基因
作者
Aya Al Othman,Dmitry V. Bagrov,Julian M. Rozenberg,Olga Glazova,Gleb Skryabin,Elena M. Tchevkina,Alexandre Mezentsev,Mikhail Durymanov
出处
期刊:Biochimica Et Biophysica Acta - General Subjects [Elsevier]
卷期号:1868 (1): 130522-130522
标识
DOI:10.1016/j.bbagen.2023.130522
摘要

Activity-regulated cytoskeleton-associated (Arc) protein is predominantly expressed in excitatory glutamatergic neurons of vertebrates, where it plays a pivotal role in regulation of synaptic plasticity. Arc protein forms capsid-like particles, which can encapsulate and transfer mRNA in extracellular vesicles (EVs) between hippocampal neurons. Once glioma cell networks actively interact with neurons via paracrine signaling and formation of neurogliomal glutamatergic synapses, we predicted the involvement of Arc in a process of EV-mediated mRNA transfer between glioma cells. Arc expression in three human glioma cell lines was evaluated by WB and immunocytochemistry. The properties of Arc protein/mRNA-containing EVs produced by glioma cells were analyzed by RT-PCR, TEM, and WB. Flow cytometry, RT-PCR, and fluorescent microscopy were used to show the involvement of Arc in EV-mediated mRNA transfer between glioma cells. It was found that human glioma cells can produce EVs containing Arc/Arg3.1 protein and Arc mRNA (or “Arc EVs”). Arc EVs from U87 glioma cells internalize and deliver Arc mRNA to recipient U87 cells, where it is translated into a protein. Arc overexpression significantly increases EV production, alters EV morphology, and enhances intercellular transfer of highly expressed mRNA in glioma cell culture. These findings indicate involvement of Arc EVs into mRNA transfer between glioma cells that could contribute to tumor progression and affect synaptic plasticity in cancer patients.
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