Exosomes/microvesicles target SARS-CoV-2 via innate and RNA-induced immunity with PIWI-piRNA system

Life Sci Alliance. 2021 Dec 3;5(3):e202101240. doi: 10.26508/lsa.202101240. Print 2022 Mar.

Abstract

Murine neural stem cells (NSCs) were recently shown to release piRNA-containing exosomes/microvesicles (Ex/Mv) for exerting antiviral immunity, but it remains unknown if these Ex/Mv could target SARS-CoV-2 and whether the PIWI-piRNA system is important for these antiviral actions. Here, using in vitro infection models, we show that hypothalamic NSCs (htNSCs) Ex/Mv provided an innate immunity protection against SARS-CoV-2. Importantly, enhanced antiviral actions were achieved by using induced Ex/Mv that were derived from induced htNSCs through twice being exposed to several RNA fragments of SARS-CoV-2 genome, a process that was designed not to involve protein translation of these RNA fragments. The increased antiviral effects of these induced Ex/Mv were associated with increased expression of piRNA species some of which could predictably target SARS-CoV-2 genome. Knockout of piRNA-interacting protein PIWIL2 in htNSCs led to reductions in both innate and induced antiviral effects of Ex/Mv in targeting SARS-CoV-2. Taken together, this study demonstrates a case suggesting Ex/Mv from certain cell types have innate and adaptive immunity against SARS-CoV-2, and the PIWI-piRNA system is important for these antiviral actions.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • A549 Cells
  • Angiotensin-Converting Enzyme 2 / metabolism
  • Animals
  • Argonaute Proteins / metabolism*
  • COVID-19 / immunology*
  • COVID-19 / metabolism*
  • Cell-Derived Microparticles / metabolism*
  • Exosomes*
  • Genome, Viral
  • Humans
  • Hypothalamus / metabolism
  • Immune System
  • Immunity, Innate
  • In Vitro Techniques
  • Mice
  • RNA / metabolism*
  • RNA, Small Interfering / metabolism*
  • SARS-CoV-2*

Substances

  • Argonaute Proteins
  • PIWIL2 protein, human
  • RNA, Small Interfering
  • RNA, immune
  • RNA
  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2