SOSTDC1-producing follicular helper T cells promote regulatory follicular T cell differentiation.
Xin WuYun WangRui HuangQujing GaiHaofei LiuMeimei ShiXiang ZhangYonglin ZuoLongjuan ChenQiwen ZhaoYu ShiFengchao WangXiaowei YanHuiping LuSenlin XuXiaohong YaoLin ChenXia ZhangQiang TianZiyan YangBo ZhongChen DongYan WangXiu-Wu BianXin-Dong LiuPublished in: Science (New York, N.Y.) (2020)
Germinal center (GC) responses potentiate the generation of follicular regulatory T (TFR) cells. However, the molecular cues driving TFR cell formation remain unknown. Here, we show that sclerostin domain-containing protein 1 (SOSTDC1), secreted by a subpopulation of follicular helper T (TFH) cells and T-B cell border-enriched fibroblastic reticular cells, is developmentally required for TFR cell generation. Fate tracking and transcriptome assessment in reporter mice establishes SOSTDC1-expressing TFH cells as a distinct T cell population that develops after SOSTDC1- TFH cells and loses the ability to help B cells for antibody production. Notably, Sostdc1 ablation in TFH cells results in substantially reduced TFR cell numbers and consequently elevated GC responses. Mechanistically, SOSTDC1 blocks the WNT-β-catenin axis and facilitates TFR cell differentiation.
Keyphrases
- induced apoptosis
- cell cycle arrest
- stem cells
- endoplasmic reticulum stress
- oxidative stress
- cell death
- type diabetes
- gene expression
- cell proliferation
- transcription factor
- signaling pathway
- crispr cas
- small molecule
- cell therapy
- epithelial mesenchymal transition
- mass spectrometry
- metabolic syndrome
- dna methylation
- high resolution
- dendritic cells
- genome wide
- gas chromatography