扎克瘦大鼠和脂肪大鼠肝细胞分泌的细胞外囊泡的脂质组学和生物分布

Maria Azparren-Angulo, Justyna Mleczko, Oihane E. Alboniga, Sergei Kruglik, Jean-Michel Guigner, Esperanza Gonzalez, Clara Garcia-Vallicrosa, Jordi Llop, Cristina Simó, Cristina Alonso, Marta Iruarrizaga, Felix Royo, Juan M. Falcon-Perez
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摘要

细胞外囊泡(EVs)与代谢综合征有关,但它们在病理发展过程中的具体作用尚不清楚。为了进一步研究 EVs 的作用,我们通过拉曼镊子显微光谱学和基于质谱的脂质组学分析了从扎克大鼠体内获得的脂肪型(ZF)和瘦肉型(ZL)肝细胞分泌的小型 EVs 群体。我们还利用正电子发射断层扫描成像技术,通过氟-18-放射性标记探索了这些 EVs 在体内和体外的生物分布。根据蛋白质与脂质的比例以及脂质的类型,我们的研究结果表明,在小型 EVs 的范围内,原代肝细胞会分泌不同亚群的颗粒。在 ZF 肝细胞分泌的 EV 中富集的甘油三酯种类也存在这些差异。生物分布实验显示,静脉注射后,EVs 在大脑、心脏、肺部、肾脏,特别是膀胱中积累。总之,我们的研究表明,与瘦肝细胞相比,脂肪肝细胞释放的 EVs 具有不同的脂质特征。生物分布实验表明,ZF 和 ZL 肝细胞分泌的 EVs 在分布上没有差异,但让我们初步了解了这些颗粒可能的靶器官。我们的研究结果可能会为病理学研究和治疗干预打开一扇大门。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Lipidomics and biodistribution of extracellular vesicles-secreted by hepatocytes from Zucker lean and fatty rats

Extracellular vesicles (EVs) have been involved in metabolic syndrome, although their specific role in the development of the pathology is still unknown. To further study the role of EVs, we have analysed by Raman tweezers microspectroscopy and mass spectrometry-based lipidomics the small EVs population secreted by fatty (ZF) and lean (ZL) hepatocytes obtained from Zucker rats. We have also explored in vivo and ex vivo biodistribution of these EVs through fluorine-18-radiolabelling using a positron emission tomography imaging. Based on the proportion of proteins to lipids and the types of lipids, our results indicate that within the range of small EVs, primary hepatocytes secrete different subpopulations of particles. These differences were observed in the enrichment of triglyceride species in EVs secreted by ZF hepatocytes. Biodistribution experiments showed accumulation in the brain, heart, lungs, kidney and specially in bladder after intravenous administration. In summary, we show that EVs released by a fatty hepatocytes carry a different lipid signature compared to their lean counterpart. Biodistribution experiment has shown no difference in the distribution of EVs secreted by ZF and ZL hepatocytes but has given us a first view of possible target organs for these particles. Our results might open a door to both pathology studies and therapeutic interventions.

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