TGF-β通过c-Maf指定TFH与TH17细胞命运在小鼠CD4+T细胞中通过c-Maf
Yinshui Chang1,2, Luisa Bach1, Marko Hasiuk3,4
1Medical Clinic III for Oncology, Hematology, Immuno-Oncology and Rheumatology, University Hospital Bonn, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.
Science immunology
|March 1, 2024
概括
转化生长因子-β (TGF-β) 能够在体外生成T卵泡辅助细胞 (TFH),这对于抗体反应至关重要. 转录因子c-Maf在TGF-β环境中指导TFH细胞命运.
科学领域:
- 免疫学 免疫学 免疫学
- 细胞生物学 细胞生物学
背景情况:
- 毛囊T辅助细胞 (TFH) 对于适应性免疫和抗体产生至关重要.
- 在试验室中产生小鼠TFH细胞具有挑战性,阻碍了对其发展的研究.
研究的目的:
- 建立一个可靠的体外协议,用于产生小鼠T毛囊辅助细胞 (TFH).
- 阐明调节TFH细胞分化的分子机制.
主要方法:
- 利用转化生长因子-β (TGF-β) 诱导激活的小鼠CD4+T细胞中的TFH细胞标记物.
- 分析了与体内TFH细胞的表型,转录和功能相似性.
- 研究了Bcl6,c-Maf和IL-2在TFH和T助手17 (TH17) 细胞分化中的作用.
主要成果:
- 在体外,TGF-β强烈诱导了TFH特征分子 (CXCR5,Bcl6).
- TGF-β诱导的TFH细胞在表型和功能上类似于体内TFH细胞,并支持B细胞反应.
- 对于TGF-β诱导的CXCR5表达,c-Maf是必需的,并且作为TFH与TH17细胞命运的切换因子.
结论:
- 使用TGF-β的新型体外系统可靠地产生功能性小鼠TFH细胞.
- c-Maf在确定TFH与TH17细胞系承诺方面发挥着关键作用.
- 了解这些途径可以了解适应性免疫和潜在的治疗点.
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