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Zucker 瘦型和肥胖型大鼠肝细胞分泌的细胞外囊泡的脂质组学与生物分布

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

作者信息

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

机构信息

Exosomes Laboratory, Center for Cooperative Research in Biosciences (CIC bioGUNE) Basque Research and Technology Alliance (BRTA), Derio Bizkaia Spain.

Metabolomics Platform, CICbioGUNE-BRTA, CIBERehd Bizkaia Technology Park, Derio Bizkaia Spain.

出版信息

J Extracell Biol. 2024 Feb 22;3(2):e140. doi: 10.1002/jex2.140. eCollection 2024 Feb.

DOI:10.1002/jex2.140
PMID:38939902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11080883/
Abstract

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.

摘要

细胞外囊泡(EVs)与代谢综合征有关,尽管它们在该病理发展中的具体作用仍不清楚。为了进一步研究细胞外囊泡的作用,我们利用拉曼镊子显微光谱法和基于质谱的脂质组学分析了从Zucker大鼠获得的脂肪性(ZF)和瘦性(ZL)肝细胞分泌的小细胞外囊泡群体。我们还通过使用正电子发射断层扫描成像的氟-18放射性标记,在体内和体外探索了这些细胞外囊泡的生物分布。基于蛋白质与脂质的比例以及脂质类型,我们的结果表明,在小细胞外囊泡范围内,原代肝细胞分泌不同亚群的颗粒。在ZF肝细胞分泌的细胞外囊泡中甘油三酯种类的富集方面观察到了这些差异。生物分布实验表明,静脉注射后,细胞外囊泡在脑、心脏、肺、肾脏中积累,特别是在膀胱中积累。总之,我们表明,脂肪性肝细胞释放的细胞外囊泡与其瘦性对应物相比具有不同的脂质特征。生物分布实验表明,ZF和ZL肝细胞分泌的细胞外囊泡在分布上没有差异,但让我们初步了解了这些颗粒可能的靶器官。我们的结果可能为病理学研究和治疗干预打开一扇门。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af78/11080883/2e29e4c4db4a/JEX2-3-e140-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af78/11080883/e1aafbef00eb/JEX2-3-e140-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af78/11080883/d620c90f9368/JEX2-3-e140-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af78/11080883/5977c3295e55/JEX2-3-e140-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af78/11080883/b7b024240664/JEX2-3-e140-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af78/11080883/2e29e4c4db4a/JEX2-3-e140-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af78/11080883/e1aafbef00eb/JEX2-3-e140-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af78/11080883/d620c90f9368/JEX2-3-e140-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af78/11080883/5977c3295e55/JEX2-3-e140-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af78/11080883/b7b024240664/JEX2-3-e140-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af78/11080883/2e29e4c4db4a/JEX2-3-e140-g003.jpg

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本文引用的文献

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2
Lipidomic analysis of adipose-derived extracellular vesicles reveals specific EV lipid sorting informative of the obesity metabolic state.脂肪细胞外囊泡的脂质组学分析揭示了特定的 EV 脂质分选,可反映肥胖的代谢状态。
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