Evidence map›Paper›PMID 41668094›Full record

ArticleJournal of neuroinflammation2026

Structural and functional modifications of neuronal lipid rafts: implications for HIV-associated neurological disorders.

Ying Fu, Kevin Huynh, Nigora Mukhamedova, Ben Crossett, Denise Tran, Siera Martinez, Anelia Horvath, Hong-Yin Wang, Ivan Castello-Serrano, Rosanna Ippolitto and 5 more

Abstract read
In one paragraph

Article in Journal of neuroinflammation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Ying FuBaker Heart and Diabetes Institute, Melbourne, VIC, 3187, Australia.
Kevin HuynhBaker Heart and Diabetes Institute, Melbourne, VIC, 3187, Australia.
Nigora MukhamedovaBaker Heart and Diabetes Institute, Melbourne, VIC, 3187, Australia.
Ben CrossettSydney Mass Spectrometry, The University of Sydney, Camperdown, NSW, 2050, Australia.
Denise TranSydney Mass Spectrometry, The University of Sydney, Camperdown, NSW, 2050, Australia.
Siera MartinezMcCormick Bioinformatics Core, Department of Biochemistry and Molecular Medicine, school of Medicine and Health Sciences, George Washington University, Washington, DC, 20037, USA.
Anelia HorvathMcCormick Bioinformatics Core, Department of Biochemistry and Molecular Medicine, school of Medicine and Health Sciences, George Washington University, Washington, DC, 20037, USA.
Hong-Yin WangDepartment of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA, 22903, USA.
Ivan Castello-SerranoDepartment of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA, 22903, USA.
Rosanna IppolittoDepartment of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA, 22903, USA.
Farhad ParhamiMAX BioPharma Inc, Santa Monica, CA, 90404, USA.
Peter J MeikleBaker Heart and Diabetes Institute, Melbourne, VIC, 3187, Australia.
Ilya LeventalDepartment of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA, 22903, USA.
Michael BukrinskyDepartment of Microbiology, Immunology and Tropical Diseases, George Washington University, Washington, DC, 20037, USA.
Dmitri SviridovBaker Heart and Diabetes Institute, Melbourne, VIC, 3187, Australia. Dmitri.Sviridov@Baker.edu.au.

Funding

SWG 2: Cure Research Scientific Working GroupP30AI117970 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI Italo Mocchetti · 2015 to 2026
$29.6M
Supplement to R01 NS124477R01NS124477 · NINDS · GEORGE WASHINGTON UNIVERSITY · PI BUKRINSKY, MICHAEL ILYA, TYOR, WILLIAM R · 2021 to 2025
$3.6M
Lipid raft therapy – a novel therapeutic approach for HIV-associated cardiometabolic co-morbiditiesR01HL158305 · NHLBI · GEORGE WASHINGTON UNIVERSITY · PI BUKRINSKY, MICHAEL ILYA, SVIRIDOV, DMITRI · 2021 to 2024
$2.6M
National Health and Medical Research Council 1197190NHLBI NIH HHS HL158305NHLBI NIH HHS R01 HL158305NIAID NIH HHS P30 AI117970NINDS NIH HHS NS124477NINDS NIH HHS R01 NS124477
6 · The paper itself

Abstract

backgroundHIV-associated neurological disorders (HAND) remain a prevalent co-morbidity of HIV infection. Growing evidence implicates the HIV protein Nef in this process, as Nef increases the abundance of neuronal lipid rafts - cholesterol- and sphingolipid-rich membrane microdomains linked to neurodegeneration and neuroinflammation. Because Nef is released from infected glial cells in extracellular vesicles (exNef), we investigated whether glia-derived exNef alters the structural and functional properties of neuronal lipid rafts in a manner that could contribute to HAND pathogenesis.

methodsA comprehensive lipidomics and proteomics analysis of lipid rafts isolated from cultured human neuronal cell line SH-SY5Y, combined with assessment of biophysical and physiological properties of the rafts, was performed. We compared our findings with existing transcriptomics profiles of brain neurons from individuals diagnosed with HAND.

resultsLipidomics analysis of isolated neuronal lipid raft fractions revealed minimal impact of exNef on the raft lipid composition; physico-chemical properties of the lipid rafts were also unaffected. In contrast, proteomic analysis revealed that among raft proteins with increased abundance following exNef exposure ~25% were implicated in neurological disease pathways. Targeted protein analysis unveiled that exNef promotes the redistribution of several neurodegenerative and inflammatory proteins to the lipid rafts, resulting in increased inflammation and apoptosis alongside reduced neuronal excitability. Pharmacological disruption of raft elevation with the lipid raft antagonist Oxy210 reversed exNef-induced raft expansion and abrogated these structural and functional alterations. Importantly, changes in raft protein composition showed strong concordance with transcriptomic profiles from single-nucleus RNA sequencing (snRNA-seq) of brain from people living with HIV.

conclusionsExNef reorganize the neuronal lipid raft proteome, enhancing the activity of neurodegenerative and inflammatory mediators. This phenomenon may potentially contribute to HAND pathogenesis.

Indexed as

AIDS Dementia ComplexHIV InfectionsMembrane MicrodomainsNervous System DiseasesNeuronsCell Line, TumorExtracellular VesiclesHumansLipidomicsNeurogliaProteomicsExtracellular vesiclesHIVHIV-associated neurological disorderLipid raftsNefNeurodegenerationNeurons

Identifiers

PMID41668094
PMCPMC12997674

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.