Author
Listed:
- Yi Tian
(Institute of Immunology, PLA, Third Military Medical University (Army Medical University))
- Chao Han
(Institute of Immunology, PLA, Third Military Medical University (Army Medical University))
- Zhiyuan Wei
(Institute of Immunology, PLA, Third Military Medical University (Army Medical University)
The First Affiliated Hospital of Third Military Medical University (Army Medical University))
- Hui Dong
(Institute of Immunology, PLA, Third Military Medical University (Army Medical University))
- Xiaohe Shen
(Shanxi Medical University)
- Yiqiang Cui
(Nanjing Medical University)
- Xiaolan Fu
(Institute of Immunology, PLA, Third Military Medical University (Army Medical University))
- Zhiqiang Tian
(Institute of Immunology, PLA, Third Military Medical University (Army Medical University))
- Shufeng Wang
(Institute of Immunology, PLA, Third Military Medical University (Army Medical University))
- Jian Zhou
(Institute of Immunology, PLA, Third Military Medical University (Army Medical University))
- Di Yang
(Institute of Immunology, PLA, Third Military Medical University (Army Medical University))
- Yi Sun
(The First Affiliated Hospital of Third Military Medical University (Army Medical University))
- Jizhao Yuan
(Institute of Immunology, PLA, Third Military Medical University (Army Medical University))
- Bing Ni
(Third Military Medical University (Army Medical University)
Key Laboratory of Extreme Environmental Medicine, Ministry of Education of China
Key Laboratory of High Altitude Medicine, PLA)
- Yuzhang Wu
(Institute of Immunology, PLA, Third Military Medical University (Army Medical University))
Abstract
T helper type 17 (Th17) cells have important functions in the pathogenesis of inflammatory and autoimmune diseases. Retinoid-related orphan receptor-γt (RORγt) is necessary for Th17 cell differentiation and functions. However, the transcriptional regulation of RORγt expression, especially at the enhancer level, is still poorly understood. Here we identify a novel enhancer of RORγt gene in Th17 cells, RORCE2. RORCE2 deficiency suppresses RORγt expression and Th17 differentiation, leading to reduced severity of experimental autoimmune encephalomyelitis. Mechanistically, RORCE2 is looped to RORγt promoter through SRY-box transcription factor 5 (SOX-5) in Th17 cells, and the loss of SOX-5 binding site in RORCE abolishes RORCE2 function and affects the binding of signal transducer and activator of transcription 3 (STAT3) to the RORγt locus. Taken together, our data highlight a molecular mechanism for the regulation of Th17 differentiation and functions, which may represent a new intervening clue for Th17-related diseases.
Suggested Citation
Yi Tian & Chao Han & Zhiyuan Wei & Hui Dong & Xiaohe Shen & Yiqiang Cui & Xiaolan Fu & Zhiqiang Tian & Shufeng Wang & Jian Zhou & Di Yang & Yi Sun & Jizhao Yuan & Bing Ni & Yuzhang Wu, 2021.
"SOX-5 activates a novel RORγt enhancer to facilitate experimental autoimmune encephalomyelitis by promoting Th17 cell differentiation,"
Nature Communications, Nature, vol. 12(1), pages 1-18, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-020-20786-w
DOI: 10.1038/s41467-020-20786-w
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-020-20786-w. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.