Safina Ksenia R, Kotliar Dylan A, Curtis Michelle, Good Jonathan D, Weng Chen, David Shawn, Raychaudhuri Soumya, Kreso Antonia, Trowbridge Jennifer, Sankaran Vijay G, van Galen Peter
Division of Hematology, Brigham and Women's Hospital, Boston, MA 02115, USA.
Department of Medicine, Harvard Medical School, Boston, MA 02115, USA.
bioRxiv. 2025 Sep 4:2025.09.01.673389. doi: 10.1101/2025.09.01.673389.
Aging of the blood system impacts systemic health and can be traced to hematopoietic stem cells (HSCs). Despite multiple reports on human HSC aging, a unified map detailing their molecular age-related changes is lacking. We developed a consensus map of gene expression in HSCs by integrating seven single-cell datasets. This map revealed previously unappreciated heterogeneity within the HSC population. It also links inflammatory pathway activation (TNF/NFκB, AP-1) and quiescence within a single gene expression program. This program dominates an inflammatory HSC subpopulation that increases with age, highlighting a potential target for further experimental studies and anti-aging interventions.
血液系统的衰老会影响全身健康,并且可以追溯到造血干细胞(HSC)。尽管有多项关于人类造血干细胞衰老的报道,但仍缺乏一份详细描述其与分子年龄相关变化的统一图谱。我们通过整合七个单细胞数据集,绘制了一份造血干细胞基因表达的共识图谱。该图谱揭示了造血干细胞群体中先前未被认识到的异质性。它还在单一基因表达程序中将炎症信号通路激活(TNF/NFκB、AP-1)与静止状态联系起来。这个程序在随着年龄增长而增加的炎症性造血干细胞亚群中占主导地位,突出了进一步实验研究和抗衰老干预的潜在靶点。