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Updated: Aug 13, 2026

Identification of EcoHIV-Infected Cells in Microglia-Manipulated Transgenic Mice
Published on: December 20, 2024
[HIV encephalopathy]
Yoshiharu Miura1, Yoshio Koyanagi
1Laboratory of Viral Pathogenesis, AIDS Research Center, Institute for Virus Research, Kyoto University.
Abstract:
HIV encephalopathy is one of the complexified viral diseases. In the infected brains, HIV-infection is restricted in macrophages and microglia although its damage extends to neurons and oligodendrocytes. Accumulating evidences have suggested that many viral and host factors are involved in this disease. However, its precise mechanism is still unsolved. To examine the mechanism of the disease, we developed an HIV-1-infected human cell-transplanted mouse model and TNF-related apoptosis-inducing ligand was identified as a neurotoxic host factors in HIV-infected brain. Next, we examined the neurotoxic host factors using co-culture system with macrophage-tropic HIV-1-infected macrophages as followings: Target brain cells are murine neuron/glia mixed culture, murine neurospehre-forming culture and rat brain hippocampus slice culture. In these systems, neurons and neural stem cells were preferentially damaged. On the other hand, we also identified two anti-HIV genes, CD 14 and CD63 (dN), which inhibit HIV-1-induced cytotoxicity using a lentiviral screening system. Because they express on monocyte or activated macrophage and microglia, these results suggest that CXCR4-using HIV-1 cannnot expand inside of brain. We also extended the screening system to identify the host factors which protect against HIV-1-induced encephalopathy. Our study will contibute to development of new therapeutic strategy for HIV encephalopathy as well as other CNS diseases.
Insights
Researchers identified TNF-related apoptosis-inducing ligand as a neurotoxic factor in HIV encephalopathy. They also found CD14 and CD63 genes that inhibit HIV-1-induced brain cell damage, offering new therapeutic targets.
Area of Science:
- Neurovirology
- Immunology
- Molecular Biology
Context:
- HIV encephalopathy is a complex viral disease affecting the brain, with damage extending to neurons despite HIV infection being restricted to macrophages and microglia.
- The precise mechanisms underlying HIV encephalopathy remain incompletely understood, necessitating further investigation into viral and host factors.
Purpose:
- To elucidate the mechanisms of HIV encephalopathy by developing a human cell-transplanted mouse model.
- To identify neurotoxic host factors and protective host factors involved in HIV-1-induced brain damage.
Summary:
- A novel HIV-1-infected human cell-transplanted mouse model was established, leading to the identification of TNF-related apoptosis-inducing ligand as a neurotoxic host factor.
- Co-culture systems revealed preferential damage to neurons and neural stem cells by HIV-1-infected macrophages.
- Two anti-HIV genes, CD14 and CD63, were identified as inhibitors of HIV-1-induced cytotoxicity, suggesting they may limit CXCR4-using HIV-1 expansion in the brain.
Impact:
- This research contributes to understanding HIV encephalopathy pathogenesis.
- Findings pave the way for developing novel therapeutic strategies for HIV encephalopathy and other central nervous system diseases.
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