Evidence map›Paper›PMID 38793575›Full record

ArticleViruses2024

EcoHIV Infection of Primary Murine Brain Cell Cultures to Model HIV Replication and Neuropathogenesis.

Boe-Hyun Kim, Wei Chao, Eran Hadas, Alejandra Borjabad, Mary Jane Potash, David J Volsky

Abstract read
In one paragraph

Article in Viruses, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. EcoHIV Infection Disrupts Dopamine and Serotonin Transporter Function, Altering Release Dynamics in C57BL/6J Mice.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. EcoHIV Infection Promotes Atherosclerosis Progression in LDLR-Deficient Mice.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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

6 authors.

Boe-Hyun KimDivision of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.ORCID 0000-0003-2821-0467
Wei ChaoDivision of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Eran HadasDivision of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Alejandra BorjabadDivision of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Mary Jane PotashDivision of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.ORCID 0000-0002-4640-8269
David J VolskyDivision of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Funding

Single cell transcriptomic and epigenomic changes during chronic HIV infection and cocaine self-administrationU01DA056003 · NIDA · ALLEN INSTITUTE · PI Paul J. Kenny, DAVID J VOLSKY · 2022 to 2026
$18.2M
Single cell brain transcriptome changes during chronic HIV infection and opiate use in conventional miceU01DA053629 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KENNY, PAUL J., VOLSKY, DAVID J · 2021 to 2025
$11.1M
Threshold of Cognitive Impairment after HIV Infection: Effect of MorphineR01DA037611 · NIDA · ST. LUKE'S-ROOSEVELT INST FOR HLTH SCIS · PI VOLSKY, DAVID J · 2014 to 2018
$4.0M
Mechanism of Cannabidiol Effects on HIV Expression, Neuroinflammation, and HIV Cognitive Disease in Chronically-infected Immunocompetent MiceR01DA052844 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BORJABAD, ALEJANDRA, KELSCHENBACH, JENNIFER L · 2020 to 2024
$3.6M
Host Glycomic Modulation of HIV-associated Neuro-inflammation During Viral SuppressionR01NS117458 · NINDS · WISTAR INSTITUTE · PI ABDEL MOHSEN, MOHAMED, NDHLOVU, LISHOMWA C · 2020 to 2023
$3.4M
Routes to enhanced HIV neuropathogenesis through expression of subclinical levels of endogenous amyloid-betaRF1NS119438 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ARANCIO, OTTAVIO, VOLSKY, DAVID J · 2022 to 2022
$2.5M
Routes to enhanced HIV neuropathogenesis through expression of subclinical levels of endogenous amyloid-betaR56NS119438 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ARANCIO, OTTAVIO, VOLSKY, DAVID J · 2020 to 2020
$869k
Routes to Enhanced HIV Neuropathogenesis Through Expression of Subclinical Levels of Endogenous Amyloid-BetaR01NS119438 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ARANCIO, OTTAVIO, VOLSKY, DAVID J · 2025 to 2025
$828k
Functional Cure of HIV Neurocognitive Disease by Induction of Innate ImmunityR21NS129460 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI POTASH, MARY JANE · 2022 to 2023
$465k
NIDA NIH HHS R01 DA037611NIDA NIH HHS R01DA037611NIDA NIH HHS R01 DA052844NIDA NIH HHS R01DA052844NIDA NIH HHS U01 DA053629NIDA NIH HHS U01DA053629NIDA NIH HHS U01 DA056003NIDA NIH HHS U01DA056003NINDS NIH HHS R01 NS117458NINDS NIH HHS R01NS117458NINDS NIH HHS R01 NS119438NINDS NIH HHS R21 129460NINDS NIH HHS R21 NS129460NINDS NIH HHS RF1R01NS119438
6 · The paper itself

Abstract

backgroundEcoHIV is a chimeric HIV that replicates in mice in CD4+ T cells, macrophages, and microglia (but not in neurons), causing lasting neurocognitive impairment resembling neurocognitive disease in people living with HIV. The present study was designed to develop EcoHIV-susceptible primary mouse brain cultures to investigate the indirect effects of HIV infection on neuronal integrity.

resultsWe used two EcoHIV clones encoding EGFP and mouse bone marrow-derived macrophages (BMM), mixed mouse brain cells, or enriched mouse glial cells from two wild-type mouse strains to test EcoHIV replication efficiency, the identity of productively infected cells, and neuronal apoptosis and integrity. EcoHIV replicated efficiently in BMM. In mixed brain cell cultures, EcoHIV targeted microglia but did not cause neuronal apoptosis. Instead, the productive infection of the microglia activated them and impaired synaptophysin expression, dendritic density, and axonal structure in the neurons. EcoHIV replication in the microglia and neuronal structural changes during infection were prevented by culture with an antiretroviral.

conclusionsIn murine brain cell cultures, EcoHIV replication in the microglia is largely responsible for the aspects of neuronal dysfunction relevant to cognitive disease in infected mice and people living with HIV. These cultures provide a tool for further study of HIV neuropathogenesis and its control.

Indexed as

BrainMicrogliaNeuronsVirus ReplicationAnimalsApoptosisCells, CulturedDisease Models, AnimalHIV-1HIV InfectionsHumansMacrophagesMiceMice, Inbred C57BLPrimary Cell CultureHIV infectionneuropathogenesisprimary brain cell cultures

Identifiers

PMID38793575
PMCPMC11125688

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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.