Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
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
_version_ 1783522729264152576
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
work_keys_str_mv AT ryanseank neuroinflammationandeif2signalingpersistdespiteantiretroviraltreatmentinanhipsctriculturemodelofhivinfection
AT gonzalezmichaelv neuroinflammationandeif2signalingpersistdespiteantiretroviraltreatmentinanhipsctriculturemodelofhivinfection
AT garifalloujamesp neuroinflammationandeif2signalingpersistdespiteantiretroviraltreatmentinanhipsctriculturemodelofhivinfection
AT bennettfrederickc neuroinflammationandeif2signalingpersistdespiteantiretroviraltreatmentinanhipsctriculturemodelofhivinfection
AT williamskimberlys neuroinflammationandeif2signalingpersistdespiteantiretroviraltreatmentinanhipsctriculturemodelofhivinfection
AT sotuyonathanielp neuroinflammationandeif2signalingpersistdespiteantiretroviraltreatmentinanhipsctriculturemodelofhivinfection
AT mironetseugene neuroinflammationandeif2signalingpersistdespiteantiretroviraltreatmentinanhipsctriculturemodelofhivinfection
AT cookkieona neuroinflammationandeif2signalingpersistdespiteantiretroviraltreatmentinanhipsctriculturemodelofhivinfection
AT hakonarsonhakon neuroinflammationandeif2signalingpersistdespiteantiretroviraltreatmentinanhipsctriculturemodelofhivinfection
AT andersonstewarta neuroinflammationandeif2signalingpersistdespiteantiretroviraltreatmentinanhipsctriculturemodelofhivinfection
AT jordansciuttokellyl neuroinflammationandeif2signalingpersistdespiteantiretroviraltreatmentinanhipsctriculturemodelofhivinfection