AI Article Synopsis

  • Plasmacytoid dendritic cells (pDCs) are key immune cells that produce type I interferons, but their role in HIV infection is not fully understood.
  • The study explored how the HIV protein Nef affects the signaling pathways and extracellular vesicle (EV) release in a human pDC cell line, GEN2.2, showing that Nef treatment leads to specific cytokine production and alters EV release.
  • Findings indicate that Nef influences pDCs differently than macrophages, suggesting important interactions that could help understand HIV pathogenesis better and pave the way for future research.

Article Abstract

Plasmacytoid dendritic cells (pDCs) are a unique dendritic cell subset specialized in type I interferon production, whose role in Human Immunodeficiency Virus (HIV) infection and pathogenesis is complex and not yet well defined. Considering the crucial role of the accessory protein Nef in HIV pathogenicity, possible alterations in intracellular signalling and extracellular vesicle (EV) release induced by exogenous Nef on uninfected pDCs have been investigated. As an experimental model system, a human plasmacytoid dendritic cell line, GEN2.2, stimulated with a myristoylated recombinant Nef protein was employed. In GEN2.2 cells, Nef treatment induced the tyrosine phosphorylation of STAT-1 and STAT-2 and the production of a set of cytokines, chemokines and growth factors including IP-10, MIP-1β, MCP-1, IL-8, TNF-α and G-CSF. The released factors differed both in type and amount from those released by macrophages treated with the same viral protein. Moreover, Nef treatment slightly reduces the production of small EVs, and the protein was found associated with the small (size < 200 nm) but not the medium/large vesicles (size > 200 nm) collected from GEN2.2 cells. These results add new information on the interactions between this virulence factor and uninfected pDCs, and may provide the basis for further studies on the interactions of Nef protein with primary pDCs.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780779PMC
http://dx.doi.org/10.3390/v14010074DOI Listing

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