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HIV-1 infection of genetically engineered iPSC-derived central nervous system-engrafted microglia in a humanized mouse model
The central nervous system (CNS) is a major human immunodeficiency virus type 1 reservoir. Microglia are the primary target cell of HIV-1 infection in the CNS. Current models have not allowed the precise molecular pathways of acute and chronic CNS microglial infection to be tested with in vivo genet...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168358/ https://www.ncbi.nlm.nih.gov/pubmed/37162838 http://dx.doi.org/10.1101/2023.04.26.538461 |
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author | Min, Alice K. Javidfar, Behnam Missall, Roy Doanman, Donald Durens, Madel Vil, Samantha St Masih, Zahra Graziani, Mara Mordelt, Annika Marro, Samuele de Witte, Lotje Chen, Benjamin K. Swartz, Talia H. Akbarian, Schahram |
author_facet | Min, Alice K. Javidfar, Behnam Missall, Roy Doanman, Donald Durens, Madel Vil, Samantha St Masih, Zahra Graziani, Mara Mordelt, Annika Marro, Samuele de Witte, Lotje Chen, Benjamin K. Swartz, Talia H. Akbarian, Schahram |
author_sort | Min, Alice K. |
collection | PubMed |
description | The central nervous system (CNS) is a major human immunodeficiency virus type 1 reservoir. Microglia are the primary target cell of HIV-1 infection in the CNS. Current models have not allowed the precise molecular pathways of acute and chronic CNS microglial infection to be tested with in vivo genetic methods. Here, we describe a novel humanized mouse model utilizing human-induced pluripotent stem cell-derived microglia to xenograft into murine hosts. These mice are additionally engrafted with human peripheral blood mononuclear cells that served as a medium to establish a peripheral infection that then spread to the CNS microglia xenograft, modeling a trans-blood-brain barrier route of acute CNS HIV-1 infection with human target cells. The approach is compatible with iPSC genetic engineering, including inserting targeted transgenic reporter cassettes to track the xenografted human cells, enabling the testing of novel treatment and viral tracking strategies in a comparatively simple and cost-effective way vivo model for neuroHIV. |
format | Online Article Text |
id | pubmed-10168358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101683582023-05-10 HIV-1 infection of genetically engineered iPSC-derived central nervous system-engrafted microglia in a humanized mouse model Min, Alice K. Javidfar, Behnam Missall, Roy Doanman, Donald Durens, Madel Vil, Samantha St Masih, Zahra Graziani, Mara Mordelt, Annika Marro, Samuele de Witte, Lotje Chen, Benjamin K. Swartz, Talia H. Akbarian, Schahram bioRxiv Article The central nervous system (CNS) is a major human immunodeficiency virus type 1 reservoir. Microglia are the primary target cell of HIV-1 infection in the CNS. Current models have not allowed the precise molecular pathways of acute and chronic CNS microglial infection to be tested with in vivo genetic methods. Here, we describe a novel humanized mouse model utilizing human-induced pluripotent stem cell-derived microglia to xenograft into murine hosts. These mice are additionally engrafted with human peripheral blood mononuclear cells that served as a medium to establish a peripheral infection that then spread to the CNS microglia xenograft, modeling a trans-blood-brain barrier route of acute CNS HIV-1 infection with human target cells. The approach is compatible with iPSC genetic engineering, including inserting targeted transgenic reporter cassettes to track the xenografted human cells, enabling the testing of novel treatment and viral tracking strategies in a comparatively simple and cost-effective way vivo model for neuroHIV. Cold Spring Harbor Laboratory 2023-04-27 /pmc/articles/PMC10168358/ /pubmed/37162838 http://dx.doi.org/10.1101/2023.04.26.538461 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Min, Alice K. Javidfar, Behnam Missall, Roy Doanman, Donald Durens, Madel Vil, Samantha St Masih, Zahra Graziani, Mara Mordelt, Annika Marro, Samuele de Witte, Lotje Chen, Benjamin K. Swartz, Talia H. Akbarian, Schahram HIV-1 infection of genetically engineered iPSC-derived central nervous system-engrafted microglia in a humanized mouse model |
title | HIV-1 infection of genetically engineered iPSC-derived central nervous system-engrafted microglia in a humanized mouse model |
title_full | HIV-1 infection of genetically engineered iPSC-derived central nervous system-engrafted microglia in a humanized mouse model |
title_fullStr | HIV-1 infection of genetically engineered iPSC-derived central nervous system-engrafted microglia in a humanized mouse model |
title_full_unstemmed | HIV-1 infection of genetically engineered iPSC-derived central nervous system-engrafted microglia in a humanized mouse model |
title_short | HIV-1 infection of genetically engineered iPSC-derived central nervous system-engrafted microglia in a humanized mouse model |
title_sort | hiv-1 infection of genetically engineered ipsc-derived central nervous system-engrafted microglia in a humanized mouse model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168358/ https://www.ncbi.nlm.nih.gov/pubmed/37162838 http://dx.doi.org/10.1101/2023.04.26.538461 |
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