Mapping Rora expression in resting and activated CD4+ T cells.

The transcription factor Rora has been shown to be important for the development of ILC2 and the regulation of ILC3, macrophages and Treg cells. Here we investigate the role of Rora across CD4+ T cells in general, but with an emphasis on Th2 cells, both in vitro as well as in the context of several...

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Autores principales: Liora Haim-Vilmovsky, Johan Henriksson, Jennifer A Walker, Zhichao Miao, Eviatar Natan, Gozde Kar, Simon Clare, Jillian L Barlow, Evelina Charidemou, Lira Mamanova, Xi Chen, Valentina Proserpio, Jhuma Pramanik, Steven Woodhouse, Anna V Protasio, Mirjana Efremova, Julian L Griffin, Matt Berriman, Gordon Dougan, Jasmin Fisher, John C Marioni, Andrew N J McKenzie, Sarah A Teichmann
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Publicado: Public Library of Science (PLoS) 2021
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spelling oai:doaj.org-article:3d39463ca138487e88bb41bb5b120a662021-12-02T20:11:19ZMapping Rora expression in resting and activated CD4+ T cells.1932-620310.1371/journal.pone.0251233https://doaj.org/article/3d39463ca138487e88bb41bb5b120a662021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0251233https://doaj.org/toc/1932-6203The transcription factor Rora has been shown to be important for the development of ILC2 and the regulation of ILC3, macrophages and Treg cells. Here we investigate the role of Rora across CD4+ T cells in general, but with an emphasis on Th2 cells, both in vitro as well as in the context of several in vivo type 2 infection models. We dissect the function of Rora using overexpression and a CD4-conditional Rora-knockout mouse, as well as a RORA-reporter mouse. We establish the importance of Rora in CD4+ T cells for controlling lung inflammation induced by Nippostrongylus brasiliensis infection, and have measured the effect on downstream genes using RNA-seq. Using a systematic stimulation screen of CD4+ T cells, coupled with RNA-seq, we identify upstream regulators of Rora, most importantly IL-33 and CCL7. Our data suggest that Rora is a negative regulator of the immune system, possibly through several downstream pathways, and is under control of the local microenvironment.Liora Haim-VilmovskyJohan HenrikssonJennifer A WalkerZhichao MiaoEviatar NatanGozde KarSimon ClareJillian L BarlowEvelina CharidemouLira MamanovaXi ChenValentina ProserpioJhuma PramanikSteven WoodhouseAnna V ProtasioMirjana EfremovaJulian L GriffinMatt BerrimanGordon DouganJasmin FisherJohn C MarioniAndrew N J McKenzieSarah A TeichmannPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 5, p e0251233 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Liora Haim-Vilmovsky
Johan Henriksson
Jennifer A Walker
Zhichao Miao
Eviatar Natan
Gozde Kar
Simon Clare
Jillian L Barlow
Evelina Charidemou
Lira Mamanova
Xi Chen
Valentina Proserpio
Jhuma Pramanik
Steven Woodhouse
Anna V Protasio
Mirjana Efremova
Julian L Griffin
Matt Berriman
Gordon Dougan
Jasmin Fisher
John C Marioni
Andrew N J McKenzie
Sarah A Teichmann
Mapping Rora expression in resting and activated CD4+ T cells.
description The transcription factor Rora has been shown to be important for the development of ILC2 and the regulation of ILC3, macrophages and Treg cells. Here we investigate the role of Rora across CD4+ T cells in general, but with an emphasis on Th2 cells, both in vitro as well as in the context of several in vivo type 2 infection models. We dissect the function of Rora using overexpression and a CD4-conditional Rora-knockout mouse, as well as a RORA-reporter mouse. We establish the importance of Rora in CD4+ T cells for controlling lung inflammation induced by Nippostrongylus brasiliensis infection, and have measured the effect on downstream genes using RNA-seq. Using a systematic stimulation screen of CD4+ T cells, coupled with RNA-seq, we identify upstream regulators of Rora, most importantly IL-33 and CCL7. Our data suggest that Rora is a negative regulator of the immune system, possibly through several downstream pathways, and is under control of the local microenvironment.
format article
author Liora Haim-Vilmovsky
Johan Henriksson
Jennifer A Walker
Zhichao Miao
Eviatar Natan
Gozde Kar
Simon Clare
Jillian L Barlow
Evelina Charidemou
Lira Mamanova
Xi Chen
Valentina Proserpio
Jhuma Pramanik
Steven Woodhouse
Anna V Protasio
Mirjana Efremova
Julian L Griffin
Matt Berriman
Gordon Dougan
Jasmin Fisher
John C Marioni
Andrew N J McKenzie
Sarah A Teichmann
author_facet Liora Haim-Vilmovsky
Johan Henriksson
Jennifer A Walker
Zhichao Miao
Eviatar Natan
Gozde Kar
Simon Clare
Jillian L Barlow
Evelina Charidemou
Lira Mamanova
Xi Chen
Valentina Proserpio
Jhuma Pramanik
Steven Woodhouse
Anna V Protasio
Mirjana Efremova
Julian L Griffin
Matt Berriman
Gordon Dougan
Jasmin Fisher
John C Marioni
Andrew N J McKenzie
Sarah A Teichmann
author_sort Liora Haim-Vilmovsky
title Mapping Rora expression in resting and activated CD4+ T cells.
title_short Mapping Rora expression in resting and activated CD4+ T cells.
title_full Mapping Rora expression in resting and activated CD4+ T cells.
title_fullStr Mapping Rora expression in resting and activated CD4+ T cells.
title_full_unstemmed Mapping Rora expression in resting and activated CD4+ T cells.
title_sort mapping rora expression in resting and activated cd4+ t cells.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/3d39463ca138487e88bb41bb5b120a66
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