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使用荧光化合物 GIF-2250/2276 测量牛奶外泌体的简单方法。

Simple methods for measuring milk exosomes using fluorescent compound GIF-2250/2276.

机构信息

Department of Chemistry and Biomolecular Science, Faculty of Engineering, Gifu University, 1-1 Yanagido, Gifu, 501-1193, Japan.

Life Science Research Center, Gifu University, Gifu, Gifu, 501-1193, Japan; The United Graduate School of Drug Discovery and Medical Information Sciences of Gifu University, 1-1 Yanagido, Gifu, 501-1193, Japan.

出版信息

Biochem Biophys Res Commun. 2024 Feb 12;696:149505. doi: 10.1016/j.bbrc.2024.149505. Epub 2024 Jan 9.

DOI:10.1016/j.bbrc.2024.149505
PMID:38219490
Abstract

Exosomes are small extracellular vesicles (EVs) found in culture supernatants, blood, and breast milk. The size of these nanocomplexes limits the methods of EV analyses. In this study, nitrobenzoxadiazole (NBD), a fluorophore, conjugated endosome-lysosome imager, GIF-2250 and its derivative, GIF-2276, were evaluated for exosome analyses. A correlation was established between GIF-2250 intensity and protein maker levels in bovine milk exosomes. We found that high-temperature sterilization milk may not contain intact exosomes. For precise analysis, we synthesized GIF-2276, which allows for the covalent attachment of NBD to the Lys residue of exosome proteins, and labeled milk exosomes were separated using a gel filtration system. GIF-2276 showed chromatographic peaks of milk exosomes containing >3 ng protein. The area (quantity) and retention time (size) of the exosome peaks were correlated to biological activity (NO synthesis suppression in RAW264.7 murine macrophages). Heat denaturation of purified milk-derived exosomes disrupted these indicators. Proteome analyses revealed GIF-2276-labeled immunomodulators, such as butyrophilin subfamily 1 member A1 and polymeric immunoglobulin receptor. The immunogenicity and quantity of these factors decreased by heat denaturation. When milk exosomes were purified from market-sourced milk we found that raw and low-temperature sterilization milk samples, contained exosomes (none in high-temperature sterilization milk). These results were also supported by transmission electron microscopy analyses. We also found that GIF-2276 could monitor exosome transportation into HEK293 cells. These results suggested that GIF-2250/2276 may be helpful to evaluate milk exosomes.

摘要

外泌体是在培养上清液、血液和母乳中发现的小细胞外囊泡 (EV)。这些纳米复合物的大小限制了 EV 分析的方法。在这项研究中,硝基苯并恶二唑 (NBD),一种荧光团,与内体溶酶体成像剂 GIF-2250 及其衍生物 GIF-2276 进行了共轭,用于外泌体分析。在牛初乳外泌体中建立了 GIF-2250 强度与蛋白标志物水平之间的相关性。我们发现高温灭菌奶可能不含有完整的外泌体。为了进行精确分析,我们合成了 GIF-2276,它允许 NBD 共价连接到外泌体蛋白的赖氨酸残基上,并使用凝胶过滤系统分离牛奶外泌体。GIF-2276 显示含有 >3ng 蛋白质的牛奶外泌体的色谱峰。外泌体峰的面积(数量)和保留时间(大小)与生物活性(RAW264.7 鼠巨噬细胞中 NO 合成抑制)相关。纯化的牛奶衍生外泌体的热变性破坏了这些指标。蛋白质组分析揭示了 GIF-2276 标记的免疫调节剂,如丁酸蛋白亚家族 1 成员 A1 和多聚免疫球蛋白受体。这些因素的免疫原性和数量因热变性而降低。当从市售牛奶中纯化牛奶外泌体时,我们发现生奶和低温灭菌奶样品中含有外泌体(高温灭菌奶中没有)。这些结果也得到透射电子显微镜分析的支持。我们还发现 GIF-2276 可以监测外泌体进入 HEK293 细胞的运输。这些结果表明 GIF-2250/2276 可能有助于评估牛奶外泌体。

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