骨桥蛋白
生物
生发中心
发病机制
免疫学
系统性红斑狼疮
转录因子
细胞分化
CD44细胞
自身免疫
T细胞
癌症研究
B细胞
细胞生物学
细胞
抗体
内科学
医学
遗传学
免疫系统
疾病
基因
作者
Ji‐Ho Park,Jongeun Lee,Yun-Jung Hur,C.C. Kim,Han Bit Kim,Dahun Um,Dasom Kim,June‐Yong Lee,Sungjun Park,Youngjae Park,Tae-Kyung Kim,Sin‐Hyeog Im,Sung Won Kim,Seung‐Ki Kwok,Yoontae Lee
标识
DOI:10.1073/pnas.2322009121
摘要
Follicular helper T (T FH ) cells mediate germinal center reactions to generate high affinity antibodies against specific pathogens, and their excessive production is associated with the pathogenesis of systemic autoimmune diseases such as systemic lupus erythematosus (SLE). ETV5, a member of the ETS transcription factor family, promotes T FH cell differentiation in mice. In this study, we examined the role of ETV5 in the pathogenesis of lupus in mice and humans. T cell–specific deletion of Etv5 alleles ameliorated T FH cell differentiation and autoimmune phenotypes in lupus mouse models. Further, we identified SPP1 as an ETV5 target that promotes T FH cell differentiation in both mice and humans. Notably, extracellular osteopontin (OPN) encoded by SPP1 enhances T FH cell differentiation by activating the CD44-AKT signaling pathway. Furthermore, ETV5 and SPP1 levels were increased in CD4 + T cells from patients with SLE and were positively correlated with disease activity. Taken together, our findings demonstrate that ETV5 is a lupus-promoting transcription factor, and secreted OPN promotes T FH cell differentiation.
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