4.7 Article

Cx43-mediated sorting of miRNAs into extracellular vesicles

期刊

EMBO REPORTS
卷 23, 期 7, 页码 -

出版社

WILEY
DOI: 10.15252/embr.202154312

关键词

Connexin43; heterogeneous nuclear ribonucleoproteins; intercellular communication; miRNA; selective sorting

资金

  1. European Regional Development Fund (ERDF) through the Operational Program for Competitiveness Factors (COMPETE) [HealthyAging2020 CENTRO-01-0145-FEDER-000012-N2323, CENTRO-01-0145-FEDER-032179, CENTRO-01-0145-FEDER-032414, POCI-01-0145-FEDER-022122, UIDB/04539/2020, UIDP/04539/2020]
  2. COST Action EU-CARDIOPROTECTION by COST (European Cooperation in Science and Technology)
  3. Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) [952266]
  4. Instituto de Salud Carlos III [PI21/00470]
  5. European Regional Development Fund (ERDF)
  6. Fundacion Cientifica Asociacion Espanola Contra el Cancer [IDEAS SEMILLA AECC 2020/IDEAS20039AASE]
  7. PPBI-Portuguese Platform of BioImaging [POCI-01-0145-FEDER-022122]
  8. iLAB - Biomaging Laboratory of the Faculty of Medicine of the University of Coimbra

向作者/读者索取更多资源

This study shows that connexin43 (Cx43) is involved in the selective sorting of miRNAs into extracellular vesicles (EV), potentially modulating cellular functions by directly binding specific miRNAs and facilitating EV-miRNA delivery.
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.

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