Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
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
_version_ 1785038840147214336
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
work_keys_str_mv AT minalicek hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel
AT javidfarbehnam hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel
AT missallroy hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel
AT doanmandonald hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel
AT durensmadel hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel
AT vilsamanthast hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel
AT masihzahra hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel
AT grazianimara hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel
AT mordeltannika hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel
AT marrosamuele hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel
AT dewittelotje hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel
AT chenbenjamink hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel
AT swartztaliah hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel
AT akbarianschahram hiv1infectionofgeneticallyengineeredipscderivedcentralnervoussystemengraftedmicrogliainahumanizedmousemodel