生物
T细胞受体
效应器
剧目
谱系(遗传)
功能(生物学)
细胞生物学
祖细胞
T细胞
细胞分化
造血
免疫学
干细胞
遗传学
基因
物理
声学
免疫系统
作者
Payam Zarin,Edward L.Y. Chen,Tracy S. H. In,Michele K. Anderson,Juan Carlos Zúñiga‐Pflücker
标识
DOI:10.1016/j.cellimm.2015.03.007
摘要
γδ T-cells boast an impressive functional repertoire that can paint them as either champions or villains depending on the environmental and immunological cues. Understanding the function of the various effector γδ subsets necessitates tracing the developmental program of these subsets, including the point of lineage bifurcation from αβ T-cells. Here, we review the importance of signals from the T-cell receptor (TCR) in determining αβ versus γδ lineage fate, and further discuss how the molecular components of this pathway may influence the developmental programming of γδ T-cells functional subsets. Additionally, we discuss the role of temporal windows in restricting the development of IL-17 producing γδ T-cell subtypes, and explore whether fetal and adult hematopoietic progenitors maintain the same potential for giving rise to this important subset.
科研通智能强力驱动
Strongly Powered by AbleSci AI