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人类 T 细胞来源外泌体的蛋白质组学分析揭示了不同的 RAS/MAPK 信号通路。

Proteomic analysis of human T cell-derived exosomes reveals differential RAS/MAPK signaling.

机构信息

Perlmutter Cancer Center, NYU School of Medicine, New York, NY, USA.

Columbia Center of Translational Immunology, Department of Medicine, Columbia University Medical Center, New York, NY, USA.

出版信息

Eur J Immunol. 2018 Nov;48(11):1915-1917. doi: 10.1002/eji.201847655. Epub 2018 Oct 3.

DOI:10.1002/eji.201847655
PMID:30207595
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6544359/
Abstract

Exosomes are cell-derived vesicles that have been implicated in the pathogenesis of many inflammatory diseases. More specifically, it has been shown that T cell-derived exosomes can induce immunological responses; however, little is known about the mechanism and the molecular content of these vesicles. Here, we used a proteomic approach to characterize human T cell-derived exosomes. We found that specific proteins of the RAS signaling pathway were enriched in exosomes derived from activated T cells, and that these vesicles induced ERK phosphorylation in recipient immune cells. Our findings support a mechanistic role of exosomes in cellular activation, and further studies should consider exosomes as a biomarker for inflammatory diseases.

摘要

外泌体是细胞来源的囊泡,已被牵连到许多炎症性疾病的发病机制中。更具体地说,已经表明 T 细胞来源的外泌体可以诱导免疫反应;然而,对于这些囊泡的机制和分子内容知之甚少。在这里,我们使用蛋白质组学方法来描述人 T 细胞来源的外泌体。我们发现,激活的 T 细胞来源的外泌体中富含 RAS 信号通路的特定蛋白质,并且这些囊泡诱导受体免疫细胞中的 ERK 磷酸化。我们的发现支持外泌体在细胞激活中的机制作用,进一步的研究应将外泌体视为炎症性疾病的生物标志物。

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