Oh Chaehwan, Mazan-Mamczarz Krystyna, Gorospe Myriam, Noh Ji Heon, Kim Kyoung Mi
Department of Biological Sciences, Chungnam National University, Daejeon, Republic of Korea.
Laboratory of Genetics and Genomics, National Institute on Aging Intramural Research Program, National Institutes of Health, Baltimore, MD, United States.
Front Cell Dev Biol. 2024 Nov 25;12:1469080. doi: 10.3389/fcell.2024.1469080. eCollection 2024.
Extracellular vesicles (EVs) are involved in cell-to-cell communication. Following uptake, EV cargo molecules, including DNA, RNA, lipids, and proteins, influence gene expression and molecular signaling in recipient cells. Although various studies have identified disease-specific EV molecules, further research into their biogenesis and secretion mechanisms is needed for clinical application. Here, we investigated the role of UPF2 in regulating the biogenesis and components of EVs. Notably, UPF2 promoted the expression of CD81, a membrane protein marker of EVs, as UPF2 silencing decreased CD81 levels in EVs, both inside the cell and secreted. In contrast, the expression levels of CD63 increased, without altering the size or numbers of EVs. In addition, reducing UPF2 levels did not affect the total number of EVs but lowered production of CD81-positive EVs and reduced the efficiency of uptake by recipient cells. Collectively, our findings uncover a novel function for UPF2 in regulating the production of CD81 and changing EV properties.
细胞外囊泡(EVs)参与细胞间通讯。被摄取后,EVs的货物分子,包括DNA、RNA、脂质和蛋白质,会影响受体细胞中的基因表达和分子信号传导。尽管各种研究已经鉴定出疾病特异性的EV分子,但要将其应用于临床,还需要进一步研究它们的生物发生和分泌机制。在此,我们研究了UPF2在调节EVs的生物发生和组成成分中的作用。值得注意的是,UPF2促进了EVs的膜蛋白标志物CD81的表达,因为UPF2沉默会降低细胞内和分泌的EVs中CD81的水平。相反,CD63的表达水平增加,而EVs的大小或数量没有改变。此外,降低UPF2水平并不影响EVs的总数,但会降低CD81阳性EVs的产生,并降低受体细胞的摄取效率。总的来说,我们的研究结果揭示了UPF2在调节CD81产生和改变EVs特性方面的新功能。