细胞生物学
PI3K/AKT/mTOR通路
激酶
细胞分化
FOXO3公司
生发中心
生物
河马信号通路
重编程
细胞
细胞生长
癌症研究
信号转导
免疫学
B细胞
抗体
蛋白激酶B
生物化学
基因
作者
Lin Dong,Yejin Cao,Hui Yang,Yueru Hou,Ying He,Yufei Wang,Qiuli Yang,Yujing Bi,Guangwei Liu
出处
期刊:Immunology
[Wiley]
日期:2022-10-10
卷期号:168 (3): 511-525
被引量:5
摘要
Follicular helper T (TFH ) cells are essential for inducing germinal centre (GC) reactions to mediate humoral adaptive immunity and antiviral effects, but the mechanisms of TFH cell differentiation remain unclear. Here, we found that the hippo kinase MST1 is critical for TFH cell differentiation, GC formation, and antibody production under steady-state conditions and viral infection. MST1 deficiency intrinsically enhanced TFH cell differentiation and GC reactions in vivo and in vitro. Mechanistically, mTOR and HIF1α signalling is involved in glucose metabolism and increased glycolysis and decreased OXPHOS, which are critically required for MST1 deficiency-directed TFH cell differentiation. Moreover, upregulated Foxo3 expression is critically responsible for TFH cell differentiation induced by Mst1-/- . Thus, our findings identify a previously unrecognized relationship between hippo kinase MST1 signalling and mTOR-HIF1α-metabolic reprogramming coupled with Foxo3 signalling in reprogramming TFH cell differentiation.
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