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In Situ Patrolling of Regulatory T Cells Is Essential for Protecting Autoimmune Exocrinopathy

https://tokushima-u.repo.nii.ac.jp/records/2000235
https://tokushima-u.repo.nii.ac.jp/records/2000235
04a50527-8994-4aeb-b743-fc476f0e5431
名前 / ファイル ライセンス アクション
pone_5_1_e8588.pdf pone_5_1_e8588.pdf (3.3 MB)
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Item type 文献 / Documents(1)
公開日 2024-10-11
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
出版社版DOI
関連識別子 https://doi.org/10.1371/journal.pone.0008588
関連名称 10.1371/journal.pone.0008588
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
タイトル
タイトル In Situ Patrolling of Regulatory T Cells Is Essential for Protecting Autoimmune Exocrinopathy
タイトル別表記
その他のタイトル Patrolling Treg Cells
著者 石丸, 直澄

× 石丸, 直澄

WEKO 1721
徳島大学 教育研究者総覧 60444/profile-ja.html
e-Rad_Researcher 60314879

ja 石丸, 直澄
ISNI

ja-Kana イシマル, ナオズミ

en Ishimaru, Naozumi

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Nitta, Takeshi

× Nitta, Takeshi

en Nitta, Takeshi

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新垣, 理恵子

× 新垣, 理恵子

WEKO 1683
e-Rad_Researcher 00193061

ja 新垣, 理恵子
ISNI

ja-Kana アラカキ, リエコ

en Arakaki, Rieko

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山田, 安希子

× 山田, 安希子

WEKO 243
e-Rad_Researcher 70452646

ja 山田, 安希子
ISNI

ja-Kana ヤマダ, アキコ

en Yamada, Akiko

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Lipp, Martin

× Lipp, Martin

en Lipp, Martin

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高浜, 洋介

× 高浜, 洋介

WEKO 1519
徳島大学 教育研究者総覧 60028/profile-ja.html
e-Rad_Researcher 20183858

ja 高浜, 洋介
ISNI

ja-Kana タカハマ, ヨウスケ

en Takahama, Yousuke

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林, 良夫

× 林, 良夫

WEKO 1659
徳島大学 教育研究者総覧 60321/profile-ja.html
e-Rad_Researcher 00127854

ja 林, 良夫
ISNI

ja-Kana ハヤシ, ヨシオ

en Hayashi, Yoshio

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抄録
内容記述 Background: Migration of T cells, including regulatory T (Treg) cells, into the secondary lymph organs is critically controlled by chemokines and adhesion molecules. However, the mechanisms by which Treg cells regulate organ-specific autoimmunity via these molecules remain unclear. Although we previously reported autoimmune exocrinopathy resembling Sjögren's syndrome (SS) in the lacrimal and salivary glands from C-C chemokine receptor 7 (CCR7)-deficient mice, it is still unclear whether CCR7 signaling might specifically affect the dynamics and functions of Treg cells in vivo. We therefore investigated the cellular mechanism for suppressive function of Treg cells via CCR7 in autoimmunity using mouse models and human samples.
Methods and Findings: Patrolling Treg cells were detected in the exocrine organs such as lacrimal and salivary glands from normal mice that tend to be targets for autoimmunity while the Treg cells were almost undetectable in the exocrine glands of CCR7−/− mice. In addition, we found the significantly increased retention of CD4+CD25+Foxp3+ Treg cells in the lymph nodes of CCR7−/− mice with aging. Although Treg cell egress requires sphingosine 1-phosphate (S1P), chemotactic function to S1P of CCR7−/− Treg cells was impaired compared with that of WT Treg cells. Moreover, the in vivo suppression activity was remarkably diminished in CCR7−/− Treg cells in the model where Treg cells were co-transferred with CCR7−/− CD25-CD4+ T cells into Rag2−/− mice. Finally, confocal analysis showed that CCR7+Treg cells were detectable in normal salivary glands while the number of CCR7+Treg cells was extremely decreased in the tissues from patients with Sjögren's syndrome.
Conclusions: These results indicate that CCR7 essentially governs the patrolling functions of Treg cells by controlling the traffic to the exocrine organs for protecting autoimmunity. Characterization of this cellular mechanism could have clinical implications by supporting development of new diagnosis or treatments for the organ-specific autoimmune diseases such as Sjögren's syndrome and clarifying how the local immune system regulates autoimmunity.
書誌情報 en : PLOS ONE

巻 5, 号 1, p. e8588, 発行日 2010-01-05
収録物ID
収録物識別子タイプ EISSN
収録物識別子 19326203
出版者
出版者 PLOS
権利情報
権利情報 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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識別子 203547
言語
言語 eng
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