Faculty of Medicine, Coimbra Institute for Clinical and Biomedical Research (iCBR), University of Coimbra, Coimbra, Portugal.
Center for Innovative Biomedicine and Biotechnology (CIBB), University of Coimbra, Coimbra, Portugal.
EMBO Rep. 2022 Jul 5;23(7):e54312. doi: 10.15252/embr.202154312. Epub 2022 May 20.
Through the exchange of lipids, proteins, and nucleic acids, extracellular vesicles (EV) allow for cell-cell communication across distant cells and tissues to regulate a wide range of physiological and pathological processes. Although some molecular mediators have been discovered, the mechanisms underlying the selective sorting of miRNAs into EV remain elusive. Previous studies demonstrated that connexin43 (Cx43) forms functional channels at the EV surface, mediating the communication with recipient cells. Here, we show that Cx43 participates in the selective sorting of miRNAs into EV through a process that can also involve RNA-binding proteins. We provide evidence that Cx43 can directly bind to specific miRNAs, namely those containing stable secondary structure elements, including miR-133b. Furthermore, Cx43 facilitates the delivery of EV-miRNAs into recipient cells. Phenotypically, we show that Cx43-mediated EV-miRNAs sorting modulates autophagy. Overall, our study ascribes another biological role to Cx43, that is, the selective incorporation of miRNAs into EV, which potentially modulates multiple biological processes in target cells and may have implications for human health and disease.
通过脂质、蛋白质和核酸的交换,细胞外囊泡(EV)允许细胞间进行远距离的细胞间通讯,从而调节广泛的生理和病理过程。尽管已经发现了一些分子介质,但 miRNA 选择性分选到 EV 中的机制仍不清楚。先前的研究表明,间隙连接蛋白 43(Cx43)在 EV 表面形成功能性通道,介导与受体细胞的通讯。在这里,我们表明 Cx43 通过一种也可能涉及 RNA 结合蛋白的过程参与 miRNA 选择性分选到 EV 中。我们提供的证据表明,Cx43 可以直接结合特定的 miRNA,即那些含有稳定二级结构元件的 miRNA,包括 miR-133b。此外,Cx43 促进 EV-miRNA 递送到受体细胞。表型上,我们表明 Cx43 介导的 EV-miRNA 分选调节自噬。总的来说,我们的研究赋予 Cx43 另一个生物学作用,即 miRNA 选择性地掺入 EV,这可能调节靶细胞中的多种生物学过程,并可能对人类健康和疾病产生影响。