Evidence map›Paper›PMID 41226631›Full record

ArticleInternational journal of molecular sciences2025

Cannabinoid Receptor Type 2 Agonist JWH-133 Stimulates Antiviral Factors and Decreases Proviral, Inflammatory, and Neurotoxic Proteins in HIV-Infected Macrophage Secretome.

Lester J Rosario-Rodríguez, Yadira M Cantres-Rosario, Ana E Rodríguez De Jesús, Alana M Mera-Pérez, Eduardo L Tosado-Rodríguez, Abiel Roche Lima, Loyda M Meléndez

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Neuroproteomic Profiling of the Anxiolytic Potential ofInternational journal of molecular sciences · 2026
    Article
  3. 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

7 authors.

Lester J Rosario-RodríguezDepartment of Internal Medicine, University of Puerto Rico-Medical Sciences Campus, San Juan, PR 00936, USA.ORCID 0000-0003-1004-152X
Yadira M Cantres-RosarioTranslational Proteomics Center, Research Capacity Core, Center for Collaborative Research in Health Disparities (CCRHD), Academic Affairs Deanship, University of Puerto Rico-Medical Sciences Campus, San Juan, PR 00936, USA.
Ana E Rodríguez De JesúsTranslational Proteomics Center, Research Capacity Core, Center for Collaborative Research in Health Disparities (CCRHD), Academic Affairs Deanship, University of Puerto Rico-Medical Sciences Campus, San Juan, PR 00936, USA.
Alana M Mera-PérezDepartment of Biology, University of Puerto Rico-Río Piedras Campus, San Juan, PR 00925, USA.
Eduardo L Tosado-RodríguezIntegrated Informatics Services, Research Capacity Core, Center for Collaborative Research in Health Disparities (CCRHD), Academic Affairs Deanship, University of Puerto Rico-Medical Sciences Campus, San Juan, PR 00936, USA.ORCID 0000-0002-9140-8671
Abiel Roche LimaIntegrated Informatics Services, Research Capacity Core, Center for Collaborative Research in Health Disparities (CCRHD), Academic Affairs Deanship, University of Puerto Rico-Medical Sciences Campus, San Juan, PR 00936, USA.ORCID 0000-0003-2246-6744
Loyda M MeléndezTranslational Proteomics Center, Research Capacity Core, Center for Collaborative Research in Health Disparities (CCRHD), Academic Affairs Deanship, University of Puerto Rico-Medical Sciences Campus, San Juan, PR 00936, USA.ORCID 0000-0003-2571-8206

Funding

SCIENCE AND TECHNOLOGY COMPETENCY & EDUCATION CORE (STCE)P20GM103475 · NIGMS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI Jose R. Rodriguez-Medina · 2012 to 2026
$52.9M
Upstream Regulation and Downstream effectors of c-MYC in Ovarian CancerU54MD007600 · NIMHD · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI Emma Fernandez-Repollet · 2017 to 2026
$35.8M
RISE Option III: MBRS RISE at the UPR Medical Sciences CampusR25GM061838 · NIGMS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI CADILLA, CARMEN LYDIA · 2000 to 2021
$25.5M
TECHNOLOGIES AND RESOURCES FOR CORE LABORATORIESU54MD007587 · NIMHD · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI LUCIANO, CARLOS A., RODRIGUEZ-MEDINA, JOSE R · 2012 to 2018
$23.2M
UCLA Short-Term Research Experience to Unlock Potential (UCLA STEP-UP)R25DK113659 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Keith C Norris · 2017 to 2026
$2.2M
Modulation of alpha-7 nicotinic acetylcholine receptor in HIV-infected microglia and brain organoidsK00NS113455 · NINDS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI ROSARIO-RODRÍGUEZ, LESTER JOSÉ · 2022 to 2025
$408k
Role of CB2R Modulation in HIV-Induced Cathepsin B NeurotoxicityF99NS113455 · NINDS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI ROSARIO-RODRÍGUEZ, LESTER JOSÉ · 2020 to 2021
$39k
NIDDK NIH HHS R25 DK113659NIGMS NIH HHS P20 GM103475NIGMS NIH HHS R25 GM061838NIMHD NIH HHS U54 MD007587NIMHD NIH HHS U54 MD007600NINDS NIH HHS F99 NS113455NINDS NIH HHS K00 NS113455
6 · The paper itself

Abstract

Although antiviral therapy has improved quality of life, around 50% of people with HIV (PWH) experience neurodegeneration and cognitive decline. This is prompted in part by the migration of HIV-infected monocyte-derived macrophages (MDMs) to the brain, leading to neuronal death. Previous studies in our lab have shown that HIV-infected MDMs secrete cathepsin B (CATB), which is a pro-inflammatory neurotoxic enzyme that is reduced by the addition of cannabinoid receptor-2 (CB2R) agonist JWH-133 to cell cultures. In this study, we aimed to identify the proteins secreted (secretome) by HIV-infected macrophages exposed to JWH-133 and quantify them using tandem mass tag (TMT) mass spectrometry. Frozen 13-day MDM supernatants from (1) an MDM negative control; (2) HIV+MDM, and (3) HIV+MDM-JWH-133 were compared in triplicate by mass spectrometry (LC/MS/MS) and analyzed for protein identification. Subsequently, the same samples were labeled by TMT labeling and quantified by LC/MS/MS. After a database search, 528 proteins were identified from all groups. Thereafter, proteins with more than three unique peptides and more than 10% coverage were selected for protein identification. Venn diagrams revealed one unique protein secreted by MDM-HIV, 10 unique proteins in HIV+MDM-JWH-133, and 15 common proteins in the three groups. CATB was unique to HIV+MDM. HIV+MDM exposed to JWH-133 showed proteins related to metabolism, cell organization, antiviral activity, and stress response. TMT analysis revealed 1454 proteins with abundance for statistical analysis based on FC ≥ |1.5| and

Indexed as

CannabinoidsHIV InfectionsMacrophagesReceptor, Cannabinoid, CB2HIV-1HumansProteomeTandem Mass Spectrometry1,1-dimethylbutyl-1-deoxy-Delta(9)-THCCannabinoidsProteomeReceptor, Cannabinoid, CB2CB2RHIV-associated neurocognitive disordersJWH-133LC/MS/MSproteomicssecretomeTMT

Identifiers

PMID41226631
PMCPMC12608856

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Registered trials

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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.