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牛乳腺肺泡MAC-T细胞为研究牛乳外泌体在药物递送中的应用提供了一种工具。

Bovine mammary alveolar MAC-T cells afford a tool for studies of bovine milk exosomes in drug delivery.

作者信息

Ogunnaike Mojisola, Wang Haichuan, Zempleni Janos

机构信息

Department of Nutrition and Health Sciences, University of Nebraska-Lincoln, Lincoln, NE, USA.

Department of Nutrition and Health Sciences, University of Nebraska-Lincoln, Lincoln, NE, USA.

出版信息

Int J Pharm. 2021 Dec 15;610:121263. doi: 10.1016/j.ijpharm.2021.121263. Epub 2021 Nov 4.

Abstract

Bovine milk exosomes (BMEs) have attracted attention as vehicles for delivering RNA therapeutics. BMEs originate in mammary alveolar cells. Here, we determined whether bovine mammary alveolar MAC-T cells afford a tool to assess RNA delivery by BMEs. MAC-T cells exosomes (MAC-T BMEs) and BMEs were harvested by differential ultracentrifugation. Exosome size, morphology, microRNA content and marker proteins were assessed using nanoparticle tracking analysis, transmission electron microscopy, real-time PCR and immunoblot analysis, respectively. MAC-T cells were genetically engineered to secrete MAC-T BMEs endogenously labeled with a near-infrared fluorescent protein and tissue distribution was compared to fluorophore-labeled BMEs following intravenous injection in C57BL/6 mice. Morphology and size were similar in MAC-T BMEs and BMEs (94 ± 5.8 nm and 101 ± 4.2 nm, p > 0.05). Both preparations expressed miR-320a, miR-200c and let-7a-5p (positive controls) but not miR-1 (negative control). Exosome marker proteins, CD9, CD63, CD81 and Tsg101, were detected in both MAC-T BMEs and BMEs. Distribution in mouse tissues was similar for both preparations, with liver being the primary accumulation site. Collectively, MAC-T BMEs afford a tool for BMEs-based RNA delivery studies.

摘要

牛乳外泌体(BMEs)作为RNA治疗药物的递送载体已引起关注。BMEs起源于乳腺腺泡细胞。在此,我们确定牛乳腺腺泡MAC-T细胞是否为评估BMEs介导的RNA递送提供了一种工具。通过差速超速离心法收集MAC-T细胞外泌体(MAC-T BMEs)和BMEs。分别使用纳米颗粒跟踪分析、透射电子显微镜、实时PCR和免疫印迹分析来评估外泌体的大小、形态、微小RNA含量和标志物蛋白。对MAC-T细胞进行基因工程改造,使其分泌内源性标记有近红外荧光蛋白的MAC-T BMEs,并在C57BL/6小鼠静脉注射后,将其组织分布与荧光团标记的BMEs进行比较。MAC-T BMEs和BMEs的形态和大小相似(分别为94±5.8nm和101±4.2nm,p>0.05)。两种制剂均表达miR-320a、miR-200c和let-7a-5p(阳性对照),但不表达miR-1(阴性对照)。在MAC-T BMEs和BMEs中均检测到外泌体标志物蛋白CD9、CD63、CD81和Tsg101。两种制剂在小鼠组织中的分布相似,肝脏是主要的蓄积部位。总体而言,MAC-T BMEs为基于BMEs的RNA递送研究提供了一种工具。

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