Satb1 regulates the effector program of encephalitogenic tissue Th17 cells in chronic inflammation

A chromatin remodelling factor Satb1 is essential for T cell lineage development in the thymus. Here the authors show that while Satb1 is dispensable for the differentiation of Th17 cells and their response to gut commensals, it plays a critical role in pathogenic Th17 effector function in EAE by di...

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Autores principales: Keiko Yasuda, Yohko Kitagawa, Ryoji Kawakami, Yoshitaka Isaka, Hitomi Watanabe, Gen Kondoh, Terumi Kohwi-Shigematsu, Shimon Sakaguchi, Keiji Hirota
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Publicado: Nature Portfolio 2019
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Acceso en línea:https://doaj.org/article/ee8dcdc2a13e4bc2b13dd9a6f3c601fd
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spelling oai:doaj.org-article:ee8dcdc2a13e4bc2b13dd9a6f3c601fd2021-12-02T17:32:40ZSatb1 regulates the effector program of encephalitogenic tissue Th17 cells in chronic inflammation10.1038/s41467-019-08404-w2041-1723https://doaj.org/article/ee8dcdc2a13e4bc2b13dd9a6f3c601fd2019-02-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-08404-whttps://doaj.org/toc/2041-1723A chromatin remodelling factor Satb1 is essential for T cell lineage development in the thymus. Here the authors show that while Satb1 is dispensable for the differentiation of Th17 cells and their response to gut commensals, it plays a critical role in pathogenic Th17 effector function in EAE by directly activating Bhlhe40 and modulating PD-1.Keiko YasudaYohko KitagawaRyoji KawakamiYoshitaka IsakaHitomi WatanabeGen KondohTerumi Kohwi-ShigematsuShimon SakaguchiKeiji HirotaNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-14 (2019)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Keiko Yasuda
Yohko Kitagawa
Ryoji Kawakami
Yoshitaka Isaka
Hitomi Watanabe
Gen Kondoh
Terumi Kohwi-Shigematsu
Shimon Sakaguchi
Keiji Hirota
Satb1 regulates the effector program of encephalitogenic tissue Th17 cells in chronic inflammation
description A chromatin remodelling factor Satb1 is essential for T cell lineage development in the thymus. Here the authors show that while Satb1 is dispensable for the differentiation of Th17 cells and their response to gut commensals, it plays a critical role in pathogenic Th17 effector function in EAE by directly activating Bhlhe40 and modulating PD-1.
format article
author Keiko Yasuda
Yohko Kitagawa
Ryoji Kawakami
Yoshitaka Isaka
Hitomi Watanabe
Gen Kondoh
Terumi Kohwi-Shigematsu
Shimon Sakaguchi
Keiji Hirota
author_facet Keiko Yasuda
Yohko Kitagawa
Ryoji Kawakami
Yoshitaka Isaka
Hitomi Watanabe
Gen Kondoh
Terumi Kohwi-Shigematsu
Shimon Sakaguchi
Keiji Hirota
author_sort Keiko Yasuda
title Satb1 regulates the effector program of encephalitogenic tissue Th17 cells in chronic inflammation
title_short Satb1 regulates the effector program of encephalitogenic tissue Th17 cells in chronic inflammation
title_full Satb1 regulates the effector program of encephalitogenic tissue Th17 cells in chronic inflammation
title_fullStr Satb1 regulates the effector program of encephalitogenic tissue Th17 cells in chronic inflammation
title_full_unstemmed Satb1 regulates the effector program of encephalitogenic tissue Th17 cells in chronic inflammation
title_sort satb1 regulates the effector program of encephalitogenic tissue th17 cells in chronic inflammation
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/ee8dcdc2a13e4bc2b13dd9a6f3c601fd
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