High salt promotes autoimmunity by TET2-induced DNA demethylation and driving the differentiation of Tfh cells

Follicular helper T cells (Tfh) have been well documented to play a critical role in autoimmunity, such as systemic lupus erythematosus (SLE), by helping B cells. In this study, high salt (sodium chloride, NaCl), under physiological conditions, was demonstrated to increase the differentiation of Tfh...

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Veröffentlicht in:Scientific reports 2016-06, Vol.6 (1), p.28065-28065, Article 28065
Hauptverfasser: Wu, Haijing, Huang, Xin, Qiu, Hong, Zhao, Ming, Liao, Wei, Yuan, Shuguang, Xie, Yubing, Dai, Yong, Chang, Christopher, Yoshimura, Akihiko, Lu, Qianjin
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Sprache:eng
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Zusammenfassung:Follicular helper T cells (Tfh) have been well documented to play a critical role in autoimmunity, such as systemic lupus erythematosus (SLE), by helping B cells. In this study, high salt (sodium chloride, NaCl), under physiological conditions, was demonstrated to increase the differentiation of Tfh. A high-salt diet markedly increased lupus features in MRL/lpr mice. The mechanism is NaCl-induced DNA demethylation via the recruitment of the hydroxytransferase Ten-Eleven Translocation 2 (TET2). Gene silencing of TET2 obviously diminished NaCl-induced Tfh cell polarization in vitro . In addition, the gene expression of sh2d1a, map3k1, spn and stat5b was enhanced after NaCl treatment, consistent with the findings in lupus CD4 + T cells. However, only spn was directly regulated by TET2 and spn was not the sole target for NaCl. Our findings not only explain the epigenetic mechanisms of high-salt induced autoimmunity but also provide an attractive molecular target for intervention strategies of patients.
ISSN:2045-2322
2045-2322
DOI:10.1038/srep28065