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Unveiling aging dynamics in the hematopoietic system insights from single-cell technologies.

Xinrong JinRuohan ZhangYunqi FuQiunan ZhuLiquan HongAiwei WuHu Wang
Published in: Briefings in functional genomics (2024)
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.
Keyphrases
  • bone marrow
  • single cell
  • rna seq
  • high throughput
  • mesenchymal stem cells
  • mass spectrometry
  • stem cells
  • oxidative stress
  • dna damage
  • cell proliferation
  • current status