Exosome delivery to the testes for dmrt1 suppression: A powerful tool for sex-determining gene studies

外体 微泡 基因传递 生物 细胞外小泡 计算生物学 细胞生物学 基因 遗传增强 生物信息学 小RNA 遗传学
作者
Tengfei Zhu,Ming Kong,Yingying Yu,Manfred Schartl,Deborah M. Power,Chen Li,Wenxiu Ma,Yongjian Sun,Shuo Li,Bowen Yue,Weijing Li,Changwei Shao
出处
期刊:Journal of Controlled Release [Elsevier]
卷期号:363: 275-289 被引量:3
标识
DOI:10.1016/j.jconrel.2023.09.027
摘要

Exosomes are endosome-derived extracellular vesicles about 100 nm in diameter. They are emerging as promising delivery platforms due to their advantages in biocompatibility and engineerability. However, research into and applications for engineered exosomes are still limited to a few areas of medicine in mammals. Here, we expanded the scope of their applications to sex-determining gene studies in early vertebrates. An integrated strategy for constructing the exosome-based delivery system was developed for efficient regulation of dmrt1, which is one of the most widely used sex-determining genes in metazoans. By combining classical methods in molecular biology and the latest technology in bioinformatics, isomiR-124a was identified as a dmrt1 inhibitor and was loaded into exosomes and a testis-targeting peptide was used to modify exosomal surface for efficient delivery. Results showed that isomiR-124a was efficiently delivered to the testes by engineered exosomes and revealed that dmrt1 played important roles in maintaining the regular structure and function of testis in juvenile fish. This is the first de novo development of an exosome-based delivery system applied in the study of sex-determining gene, which indicates an attractive prospect for the future applications of engineered exosomes in exploring more extensive biological conundrums.
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