Rodrigues Cecilia Pessoa, Shvedunova Maria, Akhtar Asifa
Department of Chromatin Regulation, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany; University of Freiburg, Faculty of Biology, Schaenzlestrasse 1, 79104 Freiburg, Germany; International Max Planck Research School for Molecular and Cellular Biology (IMPRS-MCB), Freiburg, Germany.
Department of Chromatin Regulation, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Trends Genet. 2020 Oct 21. doi: 10.1016/j.tig.2020.09.015.
Hematopoiesis is the process by which both fetal and adult organisms derive the full repertoire of blood cells from a single multipotent progenitor cell type, the hematopoietic stem cells (HSCs). Correct enactment of this process relies on a synergistic interplay between genetically encoded differentiation programs and a host of cell-intrinsic and cell-extrinsic factors. These include the influence of the HSC niche microenvironment, action of specific transcription factors, and alterations in intracellular metabolic state. The consolidation of these inputs with the genetically encoded program into a coherent differentiation program for each lineage is thought to rely on epigenetic modifiers. Recent work has delineated the precise contributions of different classes of epigenetic modifiers to HSC self-renewal as well as lineage specification and differentiation into various cell types. Here, we bring together what is currently known about chromatin status and the development of cells in the hematopoietic system under normal and abnormal conditions.
造血作用是指胎儿和成年生物体从单一的多能祖细胞类型即造血干细胞(HSC)中获得全部血细胞种类的过程。这一过程的正确实施依赖于基因编码的分化程序与众多细胞内在和外在因素之间的协同相互作用。这些因素包括HSC生态位微环境的影响、特定转录因子的作用以及细胞内代谢状态的改变。将这些输入与基因编码程序整合为每个谱系的连贯分化程序被认为依赖于表观遗传修饰因子。最近的研究已经阐明了不同类别的表观遗传修饰因子对HSC自我更新以及谱系特化和分化为各种细胞类型的确切贡献。在这里,我们汇集了目前关于正常和异常条件下造血系统中染色质状态和细胞发育的已知信息。