生物
造血
表观遗传学
免疫系统
衰老
计算生物学
造血干细胞
蛋白质组学
骨髓
免疫学
干细胞
生物信息学
细胞生物学
遗传学
DNA甲基化
基因
基因表达
作者
Xinrong Jin,Ruohan Zhang,Yunqi Fu,Qiunan Zhu,Liquan Hong,Aiwei Wu,Hu Wang
出处
期刊:Briefings in Functional Genomics
[Oxford University Press]
日期:2024-04-16
被引量:1
摘要
As the demographic structure shifts towards an aging society, strategies aimed at slowing down or reversing the aging process become increasingly essential. Aging is a major predisposing factor for many chronic diseases in humans. The hematopoietic system, comprising blood cells and their associated bone marrow microenvironment, intricately participates in hematopoiesis, coagulation, immune regulation and other physiological phenomena. The aging process triggers various alterations within the hematopoietic system, serving as a spectrum of risk factors for hematopoietic disorders, including clonal hematopoiesis, immune senescence, myeloproliferative neoplasms and leukemia. The emerging single-cell technologies provide novel insights into age-related changes in the hematopoietic system. In this review, we summarize recent studies dissecting hematopoietic system aging using single-cell technologies. We discuss cellular changes occurring during aging in the hematopoietic system at the levels of the genomics, transcriptomics, epigenomics, proteomics, metabolomics and spatial multi-omics. Finally, we contemplate the future prospects of single-cell technologies, emphasizing the impact they may bring to the field of hematopoietic system aging research.
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