Department of Pathology, Massachusetts General Hospital, Boston, MA 02114, USA.
Princess Margaret Cancer Centre, University Health Network, Toronto, ON M5G 1L7, Canada.
Cell Rep. 2018 Oct 30;25(5):1109-1117.e5. doi: 10.1016/j.celrep.2018.10.021.
Lifelong maintenance of the blood system requires equilibrium between clearance of damaged hematopoietic stem cells (HSCs) and long-term survival of the HSC pool. Severe perturbations of cellular homeostasis result in rapid HSC loss to maintain clonal purity. However, normal homeostatic processes can also generate lower-level stress; how HSCs survive these conditions remains unknown. Here we show that the integrated stress response (ISR) is uniquely active in HSCs and facilitates their persistence. Activating transcription factor 4 (ATF4) mediates the ISR and is highly expressed in HSCs due to scarcity of the eIF2 translation initiation complex. Amino acid deprivation results in eIF2α phosphorylation-dependent upregulation of ATF4, promoting HSC survival. Primitive acute myeloid leukemia (AML) cells also display eIF2 scarcity and ISR activity marks leukemia stem cells (LSCs) in primary AML samples. These findings identify a link between the ISR and stem cell survival in the normal and leukemic contexts.
血液系统的终身维持需要清除受损造血干细胞(HSCs)与 HSC 池的长期存活之间的平衡。细胞内稳态的严重破坏会导致 HSC 的快速丢失,以维持克隆纯度。然而,正常的动态平衡过程也会产生较低水平的应激;HSCs 如何在这些条件下存活仍然未知。在这里,我们表明,综合应激反应(ISR)在 HSCs 中是独特活跃的,并促进其持续存在。转录激活因子 4(ATF4)介导 ISR,由于 eIF2 翻译起始复合物的稀缺,在 HSCs 中高度表达。氨基酸剥夺导致 eIF2α 磷酸化依赖性 ATF4 的上调,促进 HSC 的存活。原始急性髓系白血病(AML)细胞也显示出 eIF2 的稀缺性,并且 ISR 活性标记原发性 AML 样本中的白血病干细胞(LSCs)。这些发现确定了正常和白血病背景下 ISR 与干细胞存活之间的联系。