成为或不成为 Treg 细胞:表观遗传机制控制的谱系决定。
To be or not to be a Treg cell: lineage decisions controlled by epigenetic mechanisms.
机构信息
Experimental Immunology, Helmholtz Centre for Infection Research, Inhoffenstrasse 7, 38124 Braunschweig, Germany.
出版信息
Sci Signal. 2011 Feb 1;4(158):pe4. doi: 10.1126/scisignal.2001783.
Regulatory T (T(reg)) cells are a unique CD4(+) T cell lineage that plays a crucial role in the maintenance of immunological tolerance. The Forkhead box transcription factor Foxp3 is critically involved in T(reg) cell development and responsible for determining the suppressive function of these cells. The majority of Foxp3(+) T(reg) cells are generated during T cell development within the thymus and show features of a stable T cell lineage. New work indicates that both induction and stabilization of Foxp3 expression are under epigenetic control, which suggests that selective interference with the underlying chromatin remodeling mechanisms might enable the development of future therapeutic strategies targeting T(reg) cells.
调节性 T(Treg)细胞是一种独特的 CD4+T 细胞谱系,在维持免疫耐受方面发挥着关键作用。叉头框转录因子 Foxp3 是 Treg 细胞发育过程中的关键因子,负责决定这些细胞的抑制功能。大多数 Foxp3+Treg 细胞是在胸腺内 T 细胞发育过程中产生的,具有稳定的 T 细胞谱系特征。新的研究表明,Foxp3 表达的诱导和稳定都受到表观遗传控制,这表明选择性干扰潜在的染色质重塑机制可能为未来靶向 Treg 细胞的治疗策略的发展提供可能。