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Updated: Jan 29, 2026

Author Spotlight: Exploring the Role of Unfolded Protein Response in HIV-1 Replication and Infectivity
Published on: June 14, 2024
HIV-1 infection modulates IL-24 expression which contributes to cell apoptosis in vitro
Scheilla Teixeira Strumillo1, Marli Ferreira Curcio1, Fábio Ferreira de Carvalho2
1Disciplina de Infectologia, Laboratório de Retrovirologia, Universidade Federal de São Paulo, São Paulo, Brazil.
Insights
Interleukin-24 (IL-24) gene and protein expression are altered during early HIV-1 infection. Neutralizing IL-24 reduced apoptosis in infected cells, suggesting a role in viral persistence.
Area of Science:
- Immunology
- Virology
- Molecular Biology
Background:
- Interleukin-24 (IL-24) is implicated in various diseases but its role in HIV-1 infection remains unclear.
- Understanding IL-24's function in early HIV-1 infection is crucial for developing new therapeutic strategies.
Purpose of the Study:
- To investigate the gene and protein expression of IL-24 in peripheral blood mononuclear cells (PBMCs) during the initial stages of HIV-1 infection.
- To assess the impact of IL-24 on apoptosis-related pathways, including caspase-3 and ERK phosphorylation, in HIV-1 infected cells.
Main Methods:
- Quantitative analysis of IL-24 gene and protein expression in PBMCs.
- Flow cytometry using Annexin V/Propidium Iodide staining to evaluate apoptosis.
- Western blot analysis for caspase-3 and phosphorylated ERK (p-ERK) expression.
- Incubation with IL-24 neutralizing antibody to assess its effect on apoptosis.
Main Results:
- HIV-1 infection significantly affected the gene and protein expression levels of IL-24 and ERK.
- Annexin V/Propidium Iodide assays showed a reduction in apoptotic mechanisms in HIV-1 infected cells following IL-24 neutralization.
- IL-24 plays a role in modulating apoptosis during early HIV-1 infection.
Conclusions:
- HIV-1 infection influences IL-24 expression and its associated apoptotic signaling pathways.
- Targeting IL-24 may offer a novel approach for antiretroviral strategies by modulating viral persistence mechanisms.
Abstract:
Although interleukin-24 (IL-24) has been extensively explored in the immunopathologies of autoimmune diseases, neoplasms, and infections, its role in HIV-1 infection has not been thoroughly elucidated to date. Therefore, the objective of this study was to evaluate the gene and protein expressions of IL-24 at the initial moments of HIV infection in PBMCs. Due to the pro-apoptotic role of IL-24, we evaluated the protein expression of caspase-3, as well as Annexin V/Propidium Iodide flow cytometry and phosphorylation of ERK, which may induce an apoptotic signal block when phosphorylated. The results of this study demonstrated that HIV-1 infection had an impact on the gene and protein expressions of IL-24 and ERK. Annexin V/Propidium Iodide assay demonstrated decrease in the mechanisms of apoptosis in infected cells after incubation of IL-24 neutralizing antibody. Studies on how HIV-1 regulates IL-24 expression may play a role in characterizing viral persistence mechanisms and designing antiretroviral strategies.
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