| Title: | HIV protein Nef expression in human microglia drives the release of distinct Nef-containing extracellular vesicles |
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| Authors: | ID Lavrin, Teja (Author)
ID Loboda, Jure (Author)
ID Ferdin, Jana (Author)
ID Levak, Valentina (Author)
ID Sitar, Simona (Author)
ID Holcar, Marija (Author)
ID Resnik, Nataša (Author)
ID Stenovec, Matjaž (Author)
ID Trampuš-Bakija, Alenka (Author)
ID Veranič, Peter (Author)
ID Žagar, Ema (Author)
ID Tušek-Žnidarič, Magda (Author)
ID Pužar Dominkuš, Pia (Author)
ID Lenassi, Metka (Author) |
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| Files: |  PDF - Presentation file, download (29,79 MB)
MD5: E3EE9E47BB92F2A1C8C53FBD67F4B329
 URL - Source URL, visit https://www.oaepublish.com/articles/evcna.2025.106
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| Language: | English |
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| Typology: | 1.01 - Original Scientific Article |
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| Organization: |  UKC LJ - Ljubljana University Medical Centre
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| Abstract: | Aim: Human immunodeficiency virus (HIV)-associated neurocognitive disorders (HAND) persist in effectively treated HIV-infected individuals, in part due to HIV reservoirs in brain microglia, which express low levels of viral proteins such as Nef. This study aimed to elucidate how microglia release Nef into the extracellular space, where it exerts its biological functions. Methods: Here, we systematically characterized extracellular particles released from immortalized human microglia (h-microglia) expressing Nef alone or after HIV infection. Importantly, we established a novel h-microglia model harboring a stably integrated Nef tagged with green fluorescent protein (Nef.GFP) transgene under an inducible promoter. Extracellular vesicles (EVs) were enriched from culture media and analyzed for morphology, size, concentration and molecular composition, including Nef content, by (super-resolution) fluorescence microscopy, (immunogold) transmission electron microscopy, asymmetric flow field-flow fractionation coupled to a multi-angle light-scattering detector, nanoparticle tracking analysis, and nano-flow cytometry and immunoblotting. Results: Nef.GFP expression increased particle release up to 11.7-fold compared with controls or known stimulants adenosine triphosphate (ATP) and ionomycin. Compared to the latter, the particles were also significantly smaller (root mean square radius, Rrms = 172 nm) and displayed unique protein and density profiles. All data support the EV nature of the released particles. Approximately half of the Nef.GFP-induced EVs contained Nef (45.5% ± 15.8%), with immunogold labeling confirming its intraluminal localization. Notably, infection with HIV isolates NL4-3 and YU-2 likewise produced Nef-positive EVs distinct from virions. Conclusion: Our findings importantly contribute to understanding the source and characteristics of extracellular Nef in the central nervous system of HIV infected individuals and offer new tools to study HIV Nef biology. Nef-laden EVs should be further investigated as potential therapeutic targets in HAND. |
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| Keywords: | human immunodeficiency virus (HIV), microglia, protein Nef, extracellular vesicles (EVs), HIV-associated neurocognitive disorder (HAND) |
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| Publication status: | Published |
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| Publication version: | Version of Record |
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| Year of publishing: | 2025 |
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| Number of pages: | str. 895-920 |
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| Numbering: | Vol. 6, iss. 4 |
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| PID: | 20.500.12556/DiRROS-28905  |
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| UDC: | 616.9 |
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| ISSN on article: | 2767-6641 |
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| DOI: | 10.20517/evcna.2025.106 |
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| COBISS.SI-ID: | 259787779 |
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| Note: | Nasl. z nasl. zaslona;
Opis vira z dne 3. 12. 2025;
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| Publication date in DiRROS: | 13.04.2026 |
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| Views: | 39 |
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| Downloads: | 15 |
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