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Neuroinflammation and EIF2 Signaling Persist despite Antiretroviral Treatment in an hiPSC Tri-culture Model of HIV Infection
HIV-associated neurocognitive disorders (HAND) affect over half of HIV-infected individuals, despite antiretroviral therapy (ART). Therapeutically targetable mechanisms underlying HAND remain elusive, partly due to a lack of a representative model. We developed a human-induced pluripotent stem cell...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160309/ https://www.ncbi.nlm.nih.gov/pubmed/32220329 http://dx.doi.org/10.1016/j.stemcr.2020.02.010 |
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author | Ryan, Sean K. Gonzalez, Michael V. Garifallou, James P. Bennett, Frederick C. Williams, Kimberly S. Sotuyo, Nathaniel P. Mironets, Eugene Cook, Kieona Hakonarson, Hakon Anderson, Stewart A. Jordan-Sciutto, Kelly L. |
author_facet | Ryan, Sean K. Gonzalez, Michael V. Garifallou, James P. Bennett, Frederick C. Williams, Kimberly S. Sotuyo, Nathaniel P. Mironets, Eugene Cook, Kieona Hakonarson, Hakon Anderson, Stewart A. Jordan-Sciutto, Kelly L. |
author_sort | Ryan, Sean K. |
collection | PubMed |
description | HIV-associated neurocognitive disorders (HAND) affect over half of HIV-infected individuals, despite antiretroviral therapy (ART). Therapeutically targetable mechanisms underlying HAND remain elusive, partly due to a lack of a representative model. We developed a human-induced pluripotent stem cell (hiPSC)-based model, independently differentiating hiPSCs into neurons, astrocytes, and microglia, and systematically combining to generate a tri-culture with or without HIV infection and ART. Single-cell RNA sequencing analysis on tri-cultures with HIV-infected microglia revealed inflammatory signatures in the microglia and EIF2 signaling in all three cell types. Treatment with the antiretroviral compound efavirenz (EFZ) mostly resolved these signatures. However, EFZ increased RhoGDI and CD40 signaling in the HIV-infected microglia. This activation was associated with a persistent increase in transforming growth factor α production by microglia. This work establishes a tri-culture that recapitulates key features of HIV infection in the CNS and provides a new model to examine the effects of infection, its treatment, and other co-morbid conditions. |
format | Online Article Text |
id | pubmed-7160309 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-71603092020-04-22 Neuroinflammation and EIF2 Signaling Persist despite Antiretroviral Treatment in an hiPSC Tri-culture Model of HIV Infection Ryan, Sean K. Gonzalez, Michael V. Garifallou, James P. Bennett, Frederick C. Williams, Kimberly S. Sotuyo, Nathaniel P. Mironets, Eugene Cook, Kieona Hakonarson, Hakon Anderson, Stewart A. Jordan-Sciutto, Kelly L. Stem Cell Reports Article HIV-associated neurocognitive disorders (HAND) affect over half of HIV-infected individuals, despite antiretroviral therapy (ART). Therapeutically targetable mechanisms underlying HAND remain elusive, partly due to a lack of a representative model. We developed a human-induced pluripotent stem cell (hiPSC)-based model, independently differentiating hiPSCs into neurons, astrocytes, and microglia, and systematically combining to generate a tri-culture with or without HIV infection and ART. Single-cell RNA sequencing analysis on tri-cultures with HIV-infected microglia revealed inflammatory signatures in the microglia and EIF2 signaling in all three cell types. Treatment with the antiretroviral compound efavirenz (EFZ) mostly resolved these signatures. However, EFZ increased RhoGDI and CD40 signaling in the HIV-infected microglia. This activation was associated with a persistent increase in transforming growth factor α production by microglia. This work establishes a tri-culture that recapitulates key features of HIV infection in the CNS and provides a new model to examine the effects of infection, its treatment, and other co-morbid conditions. Elsevier 2020-03-26 /pmc/articles/PMC7160309/ /pubmed/32220329 http://dx.doi.org/10.1016/j.stemcr.2020.02.010 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Ryan, Sean K. Gonzalez, Michael V. Garifallou, James P. Bennett, Frederick C. Williams, Kimberly S. Sotuyo, Nathaniel P. Mironets, Eugene Cook, Kieona Hakonarson, Hakon Anderson, Stewart A. Jordan-Sciutto, Kelly L. Neuroinflammation and EIF2 Signaling Persist despite Antiretroviral Treatment in an hiPSC Tri-culture Model of HIV Infection |
title | Neuroinflammation and EIF2 Signaling Persist despite Antiretroviral Treatment in an hiPSC Tri-culture Model of HIV Infection |
title_full | Neuroinflammation and EIF2 Signaling Persist despite Antiretroviral Treatment in an hiPSC Tri-culture Model of HIV Infection |
title_fullStr | Neuroinflammation and EIF2 Signaling Persist despite Antiretroviral Treatment in an hiPSC Tri-culture Model of HIV Infection |
title_full_unstemmed | Neuroinflammation and EIF2 Signaling Persist despite Antiretroviral Treatment in an hiPSC Tri-culture Model of HIV Infection |
title_short | Neuroinflammation and EIF2 Signaling Persist despite Antiretroviral Treatment in an hiPSC Tri-culture Model of HIV Infection |
title_sort | neuroinflammation and eif2 signaling persist despite antiretroviral treatment in an hipsc tri-culture model of hiv infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160309/ https://www.ncbi.nlm.nih.gov/pubmed/32220329 http://dx.doi.org/10.1016/j.stemcr.2020.02.010 |
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