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Exosomes/microvesicles target SARS-CoV-2 via innate and RNA-induced immunity with PIWI-piRNA system
Shoeb Ikhlas1, Afia Usman1, Dongkyeong Kim1
1Department of Molecular Pharmacology, Albert Einstein College of Medicine, New York City, NY, USA.
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.
Insights
Hypothalamic neural stem cell (NSC) exosomes offer innate immunity against SARS-CoV-2. The PIWI-piRNA system enhances these antiviral effects, suggesting a novel therapeutic avenue.
Area of Science:
- Neuroscience
- Immunology
- Virology
Background:
- Neural stem cells (NSCs) release exosomes/microvesicles (Ex/Mv) with piRNAs for antiviral immunity.
- The role of NSC-derived Ex/Mv against SARS-CoV-2 and the PIWI-piRNA system's involvement remain unclear.
Purpose of the Study:
- To investigate if hypothalamic NSC (htNSC) Ex/Mv can target SARS-CoV-2.
- To determine the importance of the PIWI-piRNA system in these antiviral actions.
Main Methods:
- In vitro infection models using hypothalamic NSCs (htNSCs).
- Generation of induced Ex/Mv from htNSCs exposed to SARS-CoV-2 RNA fragments.
- Knockout of PIWIL2 in htNSCs to assess its role.
Main Results:
- htNSC Ex/Mv demonstrated innate immunity against SARS-CoV-2 in vitro.
- Induced Ex/Mv, derived from SARS-CoV-2 RNA-exposed htNSCs, showed enhanced antiviral activity.
- Increased piRNA species in induced Ex/Mv were associated with predictable targeting of the SARS-CoV-2 genome.
- PIWIL2 knockout in htNSCs reduced both innate and induced antiviral effects of Ex/Mv.
Conclusions:
- Exosomes/microvesicles from specific cell types, like htNSCs, possess innate and adaptive immunity against SARS-CoV-2.
- The PIWI-piRNA system is crucial for mediating these Ex/Mv-driven antiviral responses.
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