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外泌体介导的胰岛素递送用于糖尿病的潜在治疗

Exosome-Mediated Insulin Delivery for the Potential Treatment of Diabetes Mellitus.

作者信息

Rodríguez-Morales Belén, Antunes-Ricardo Marilena, González-Valdez José

机构信息

School of Engineering and Science, Tecnologico de Monterrey, Av. Eugenio Garza Sada 2501 Sur, Monterrey 64849, NL, Mexico.

出版信息

Pharmaceutics. 2021 Nov 5;13(11):1870. doi: 10.3390/pharmaceutics13111870.

Abstract

Exosomes are extracellular nanovesicles between 30 and 150 nm that serve as essential messengers for different biological signaling and pathological processes. After their discovery, a wide range of applications have been developed, especially in therapeutic drug delivery. In this context, the aim of this work was to test the efficiency of exosome-mediated human insulin delivery using exosomes extracted from three different cell lines: hepatocellular carcinoma (HepG2); primary dermal fibroblasts (HDFa) and pancreatic β cells (RIN-m); all are related to the production and/or the ability to sense insulin and to consequently regulate glucose levels in the extracellular medium. The obtained results revealed that the optimal insulin loading efficiency was achieved by a 200 V electroporation, in comparison with incubation at room temperature. Moreover, the maximum in vitro exosome uptake was reached after incubation for 6 h, which slightly decreased 24 h after adding the exosomes. Glucose quantification assays revealed that exosome-mediated incorporation of insulin presented significant differences in HDFa and HepG2 cells, enhancing the transport in HDFa, in comparison with free human insulin effects in the regulation of extracellular glucose levels. No significant differences were found between the treatments in RIN-m cells. Hence, the results suggest that exosomes could potentially become a valuable tool for stable and biocompatible insulin delivery in diabetes mellitus treatment alternatives.

摘要

外泌体是直径在30到150纳米之间的细胞外纳米囊泡,是不同生物信号传导和病理过程的重要信使。自被发现以来,外泌体已得到广泛应用,尤其是在治疗性药物递送方面。在此背景下,本研究旨在测试利用从三种不同细胞系中提取的外泌体介导人胰岛素递送的效率,这三种细胞系分别为:肝癌细胞系(HepG2)、原代表皮成纤维细胞(HDFa)和胰腺β细胞(RIN-m);所有这些细胞系均与胰岛素的产生和/或感知能力有关,并因此能够调节细胞外培养基中的葡萄糖水平。所得结果表明,与室温孵育相比,通过200V电穿孔可实现最佳胰岛素负载效率。此外,孵育6小时后体外外泌体摄取量达到最大值,添加外泌体24小时后摄取量略有下降。葡萄糖定量分析表明,外泌体介导的胰岛素掺入在HDFa和HepG2细胞中存在显著差异,与游离人胰岛素调节细胞外葡萄糖水平的效果相比,外泌体增强了HDFa中的转运。在RIN-m细胞的处理之间未发现显著差异。因此,结果表明外泌体有可能成为糖尿病治疗替代方案中稳定且生物相容的胰岛素递送的有价值工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4668/8621140/db1dcd1c9901/pharmaceutics-13-01870-g001.jpg

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