Department of Hematology, Oncology and Stem Cell Transplantation, Medical Center, University of Freiburg, Faculty of Medicine, Hugstetter Strasse 55, 79106, Freiburg, Germany.
Faculty of Biology, University of Freiburg, Schaenzlestrasse 1, 79104, Freiburg, Germany.
Cell Mol Life Sci. 2019 Jan;76(2):369-380. doi: 10.1007/s00018-018-2952-3. Epub 2018 Oct 24.
Hematopoietic stem and progenitor cells (HSPCs) represent the lifelong source of all blood cells and continuously regenerate the hematopoietic system through differentiation and self-renewal. The process of differentiation is initiated in the G phase of the cell cycle, when stem cells leave their quiescent state. During G, the anaphase-promoting complex or cyclosome associated with the coactivator Cdh1 is highly active and marks proteins for proteasomal degradation to regulate cell proliferation. Following Cdh1 knockdown in HSPCs, we analyzed human and mouse hematopoiesis in vitro and in vivo in competitive transplantation assays. We found that Cdh1 is highly expressed in human CD34 HSPCs and downregulated in differentiated subsets; whereas, loss of Cdh1 restricts myeloid differentiation, supports B cell development and preserves immature short-term HSPCs without affecting proliferation or viability. Our data highlight a role of Cdh1 as a regulator of balancing the maintenance of HSPCs and differentiation into mature blood cells.
造血干细胞和祖细胞 (HSPCs) 代表所有血细胞的终身来源,并通过分化和自我更新不断再生造血系统。分化过程始于细胞周期的 G 期,此时干细胞离开静止状态。在 G 期,与共激活因子 Cdh1 相关的后期促进复合物或 cyclosome 非常活跃,并标记蛋白质进行蛋白酶体降解,以调节细胞增殖。在 HSPCs 中敲低 Cdh1 后,我们在体外和体内竞争移植实验中分析了人类和小鼠的造血。我们发现 Cdh1 在人类 CD34 HSPCs 中高度表达,并在分化亚群中下调;然而,Cdh1 的缺失限制了髓系分化,支持 B 细胞发育,并保留未成熟的短期 HSPCs,而不影响增殖或活力。我们的数据强调了 Cdh1 作为平衡 HSPCs 维持和分化为成熟血细胞的调节剂的作用。