A BMPR2/YY1 Signaling Axis Is Required for Human Cytomegalovirus Latency in Undifferentiated Myeloid Cells

Understanding the mechanisms which regulate HCMV latency could allow therapeutic targeting of the latent virus reservoir from where virus reactivation can cause severe disease. We show that the BMPR2/TGFbeta receptor/YY1 signaling axis is crucial to maintain HCMV latency in undifferentiated cells a...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Emma Poole, Maria Cristina Carlan da Silva, Chris Huang, Marianne Perera, Sarah Jackson, Ian J. Groves, Mark Wills, Amer Rana, John Sinclair
Formato: article
Lenguaje:EN
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://doaj.org/article/c5a89e14f27243eba150c45f5244720d
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:c5a89e14f27243eba150c45f5244720d
record_format dspace
spelling oai:doaj.org-article:c5a89e14f27243eba150c45f5244720d2021-11-03T21:15:02ZA BMPR2/YY1 Signaling Axis Is Required for Human Cytomegalovirus Latency in Undifferentiated Myeloid Cells2150-751110.1128/mBio.00227-21https://doaj.org/article/c5a89e14f27243eba150c45f5244720d2021-06-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.00227-21https://doaj.org/toc/2150-7511 Understanding the mechanisms which regulate HCMV latency could allow therapeutic targeting of the latent virus reservoir from where virus reactivation can cause severe disease. We show that the BMPR2/TGFbeta receptor/YY1 signaling axis is crucial to maintain HCMV latency in undifferentiated cells and that pharmacological reduction of BMPR2 in latently infected cells leads to reactivation of the viral lytic transcription program, which renders the infected cell open to immune detection and clearance in infected individuals.Emma PooleMaria Cristina Carlan da SilvaChris HuangMarianne PereraSarah JacksonIan J. GrovesMark WillsAmer RanaJohn SinclairAmerican Society for MicrobiologyarticleMicrobiologyQR1-502ENmBio, Vol 12, Iss 3 (2021)
institution DOAJ
collection DOAJ
language EN
topic Microbiology
QR1-502
spellingShingle Microbiology
QR1-502
Emma Poole
Maria Cristina Carlan da Silva
Chris Huang
Marianne Perera
Sarah Jackson
Ian J. Groves
Mark Wills
Amer Rana
John Sinclair
A BMPR2/YY1 Signaling Axis Is Required for Human Cytomegalovirus Latency in Undifferentiated Myeloid Cells
description Understanding the mechanisms which regulate HCMV latency could allow therapeutic targeting of the latent virus reservoir from where virus reactivation can cause severe disease. We show that the BMPR2/TGFbeta receptor/YY1 signaling axis is crucial to maintain HCMV latency in undifferentiated cells and that pharmacological reduction of BMPR2 in latently infected cells leads to reactivation of the viral lytic transcription program, which renders the infected cell open to immune detection and clearance in infected individuals.
format article
author Emma Poole
Maria Cristina Carlan da Silva
Chris Huang
Marianne Perera
Sarah Jackson
Ian J. Groves
Mark Wills
Amer Rana
John Sinclair
author_facet Emma Poole
Maria Cristina Carlan da Silva
Chris Huang
Marianne Perera
Sarah Jackson
Ian J. Groves
Mark Wills
Amer Rana
John Sinclair
author_sort Emma Poole
title A BMPR2/YY1 Signaling Axis Is Required for Human Cytomegalovirus Latency in Undifferentiated Myeloid Cells
title_short A BMPR2/YY1 Signaling Axis Is Required for Human Cytomegalovirus Latency in Undifferentiated Myeloid Cells
title_full A BMPR2/YY1 Signaling Axis Is Required for Human Cytomegalovirus Latency in Undifferentiated Myeloid Cells
title_fullStr A BMPR2/YY1 Signaling Axis Is Required for Human Cytomegalovirus Latency in Undifferentiated Myeloid Cells
title_full_unstemmed A BMPR2/YY1 Signaling Axis Is Required for Human Cytomegalovirus Latency in Undifferentiated Myeloid Cells
title_sort bmpr2/yy1 signaling axis is required for human cytomegalovirus latency in undifferentiated myeloid cells
publisher American Society for Microbiology
publishDate 2021
url https://doaj.org/article/c5a89e14f27243eba150c45f5244720d
work_keys_str_mv AT emmapoole abmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT mariacristinacarlandasilva abmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT chrishuang abmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT marianneperera abmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT sarahjackson abmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT ianjgroves abmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT markwills abmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT amerrana abmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT johnsinclair abmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT emmapoole bmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT mariacristinacarlandasilva bmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT chrishuang bmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT marianneperera bmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT sarahjackson bmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT ianjgroves bmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT markwills bmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT amerrana bmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
AT johnsinclair bmpr2yy1signalingaxisisrequiredforhumancytomegaloviruslatencyinundifferentiatedmyeloidcells
_version_ 1718445421069598720