Department of Developmental Biology and Cancer Research, Institute for Medical Research Israel-Canada, Hebrew University Medical School, P.O.B. 12272, Ein Kerem, Jerusalem, Israel, 91120.
Nat Rev Immunol. 2011 Jun 10;11(7):478-88. doi: 10.1038/nri2991.
Cells of the immune system are generated through a developmental cascade that begins in haematopoietic stem cells. During this process, gene expression patterns are programmed in a series of stages that bring about the restriction of cell potential, ultimately leading to the formation of specialized innate immune cells and mature lymphocytes that express antigen receptors. These events involve the regulation of both gene expression and DNA recombination, mainly through the control of chromatin accessibility. In this Review, we describe the epigenetic changes that mediate this complex differentiation process and try to understand the logic of the programming mechanism.
免疫系统细胞是通过一个始于造血干细胞的发育级联产生的。在这个过程中,基因表达模式在一系列阶段中被编程,这些阶段带来细胞潜能的限制,最终导致形成专门的先天免疫细胞和表达抗原受体的成熟淋巴细胞。这些事件涉及基因表达和 DNA 重组的调节,主要通过控制染色质可及性来实现。在这篇综述中,我们描述了介导这一复杂分化过程的表观遗传变化,并试图理解编程机制的逻辑。