HIV‐1 Nef is carried on the surface of extracellular vesicles

Author:

Vanpouille Christophe1,Brichacek Beda2,Pushkarsky Tatiana2,Dubrovsky Larisa2,Fitzgerald Wendy1,Mukhamedova Nigora3,Garcia‐Hernandez Sofia4,Matthies Doreen5,Popratiloff Anastas4,Sviridov Dmitri36,Margolis Leonid17,Bukrinsky Michael2ORCID

Affiliation:

1. Section on Intercellular Interactions, Eunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health Bethesda Maryland USA

2. Department of Microbiology, Immunology and Tropical Medicine The George Washington University School of Medicine and Health Sciences Washington District of Columbia USA

3. Baker Heart and Diabetes Institute Melbourne VIC Australia

4. Nanofabrication and Imaging Center The George Washington University Washington District of Columbia USA

5. Unit on Structural Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health Bethesda Maryland USA

6. Department of Biochemistry and Molecular Biology Monash University Clayton VIC Australia

7. Faculty of Natural Sciences and Medicine Ilia State University Tbilisi Republic of Georgia

Abstract

AbstractExtracellular vesicles (EVs) serve as pivotal mediators of intercellular communication in both health and disease, delivering biologically active molecules from vesicle‐producing cells to recipient cells. In the context of HIV infection, EVs have been shown to carry the viral protein Nef, a key pathogenic factor associated with HIV‐related co‐morbidities. Despite this recognition, the specific localisation of Nef within the vesicles has remained elusive. This study addresses this critical knowledge gap by investigating Nef‐containing EVs. Less than 1% of the total released Nef was associated with EVs; most Nef existed as free protein released by damaged cells. Nevertheless, activity of EV‐associated Nef in downregulating the major cholesterol transporter ABCA1, a critical aspect linked to the pathogenic effects of Nef, was comparable to that of free Nef present in the supernatant. Through a series of biochemical and microscopic assays, we demonstrate that the majority of EV‐associated Nef molecules are localised on the external surface of the vesicles. This distinctive distribution prompts the consideration of Nef‐containing EVs as potential targets for immunotherapeutic interventions aimed at preventing or treating HIV‐associated co‐morbidities. In conclusion, our results shed light on the localisation and functional activity of Nef within EVs, providing valuable insights for the development of targeted immunotherapies to mitigate the impact of HIV‐associated co‐morbidities.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Institute of Neurological Disorders and Stroke

National Institute of Allergy and Infectious Diseases

Publisher

Wiley

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