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从正常和高脂肪百分比的血浆受试者中分离外泌体的方法比较。

Comparison of Methods for Isolating Exosomes from Plasma Subjects with Normal and High Fat Percentages.

作者信息

Noboa-Velástegui Jacqueline, León Juan Carlos, Castro Jorge, Fletes Ana, Madrigal Perla, Álvarez Iñaki, Navarro Rosa

机构信息

Doctorado en Ciencias Biomédicas, Secretaría Académica, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Calle Sierra Mojada No. 950, Colonia Independencia, Guadalajara C.P. 44340, Mexico.

Departamento de Biología Celular, Fisiología e Inmnunología, Institut de Biotecnologia i Biomedicina, Campus de Bellaterra, Bellatera, 08193 Barcelona, Spain.

出版信息

Life (Basel). 2025 Mar 6;15(3):410. doi: 10.3390/life15030410.

DOI:10.3390/life15030410
PMID:40141758
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11943918/
Abstract

Adipose tissue is responsible for fat storage and is an important producer of extracellular vesicles (EVs). The biological content of exosomes, one kind of EV, provides information on aspects such as immunometabolic alterations. This study aimed to compare three plasma exosome isolation methods-using a commercial kit (CK), size exclusion chromatography (SEC), and differential centrifugation (DC)-and select the best one. Individuals categorized by normal and high body fat percentages were used. The DC and CK were proven to be the most advantageous out of the exosome isolation methods, so we suggest these methods for further protein and molecular analyses, respectively. Still, we emphasize the importance of selecting an appropriate methodology depending on the specific research objectives. At the same time, no statistical differences in exosome quality, morphology, total protein, or concentration were observed between individuals categorized by body fat percentage, so we suggest that the exosomal cargo varies in individuals with normal and high fat percentages.

摘要

脂肪组织负责脂肪储存,是细胞外囊泡(EVs)的重要产生者。外泌体是EVs的一种,其生物学内容提供了有关免疫代谢改变等方面的信息。本研究旨在比较三种血浆外泌体分离方法——使用商业试剂盒(CK)、尺寸排阻色谱法(SEC)和差速离心法(DC)——并选择最佳方法。使用了按正常和高体脂百分比分类的个体。在所有外泌体分离方法中,DC和CK被证明是最具优势的,因此我们分别建议将这些方法用于进一步的蛋白质和分子分析。不过,我们强调根据具体研究目标选择合适方法的重要性。同时,按体脂百分比分类的个体之间在外泌体质量、形态、总蛋白或浓度方面未观察到统计学差异,因此我们认为正常和高脂肪百分比个体的外泌体货物存在差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49e3/11943918/fafecb90f184/life-15-00410-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49e3/11943918/07dcf712e72b/life-15-00410-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49e3/11943918/7c7fab88b88d/life-15-00410-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49e3/11943918/fafecb90f184/life-15-00410-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49e3/11943918/07dcf712e72b/life-15-00410-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49e3/11943918/7c7fab88b88d/life-15-00410-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49e3/11943918/fafecb90f184/life-15-00410-g003.jpg

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本文引用的文献

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Transl Oncol. 2024 Dec;50:102121. doi: 10.1016/j.tranon.2024.102121. Epub 2024 Sep 14.
2
The association between the size of adipocyte-derived extracellular vesicles and fasting serum triglyceride-glucose index as proxy measures of adipose tissue insulin resistance in a rat model of early-stage obesity.在早期肥胖大鼠模型中,脂肪细胞衍生的细胞外囊泡大小与空腹血清甘油三酯-葡萄糖指数之间的关联,作为脂肪组织胰岛素抵抗的替代指标。
Front Nutr. 2024 Jul 1;11:1387521. doi: 10.3389/fnut.2024.1387521. eCollection 2024.
3
Therapeutic Applications of Stem Cell-Derived Exosomes.
干细胞衍生的外泌体的治疗应用。
Int J Mol Sci. 2024 Mar 21;25(6):3562. doi: 10.3390/ijms25063562.
4
Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches.细胞外囊泡研究的最低信息要求(MISEV2023):从基础到先进方法。
J Extracell Vesicles. 2024 Feb;13(2):e12404. doi: 10.1002/jev2.12404.
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Adipocyte-derived extracellular vesicles: bridging the communications between obesity and tumor microenvironment.脂肪细胞衍生的细胞外囊泡:架起肥胖与肿瘤微环境之间的沟通桥梁。
Discov Oncol. 2023 Jun 8;14(1):92. doi: 10.1007/s12672-023-00704-4.
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Adipose tissue-derived exosomes contribute to obesity-associated liver diseases in long-term high-fat diet-fed mice, but not in short-term.脂肪组织来源的外泌体在长期高脂饮食喂养的小鼠中会导致肥胖相关的肝脏疾病,但在短期喂养中不会。
Front Nutr. 2023 May 9;10:1162992. doi: 10.3389/fnut.2023.1162992. eCollection 2023.
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