揭示造血系统中的衰老动态:来自单细胞技术的见解

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

作者信息

Jin Xinrong, Zhang Ruohan, Fu Yunqi, Zhu Qiunan, Hong Liquan, Wu Aiwei, Wang Hu

机构信息

Zhejiang Key Laboratory of Medical Epigenetics, School of Basic Medical Sciences, The Third People's Hospital of Deqing, Deqing Hospital of Hangzhou Normal University, Hangzhou Normal University, Hangzhou 311121, China.

出版信息

Brief Funct Genomics. 2024 Sep 27;23(5):639-650. doi: 10.1093/bfgp/elae019.

Abstract

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.

摘要

随着人口结构向老龄化社会转变,旨在减缓或逆转衰老过程的策略变得越来越重要。衰老是人类许多慢性疾病的主要诱发因素。造血系统由血细胞及其相关的骨髓微环境组成,复杂地参与造血、凝血、免疫调节等生理现象。衰老过程引发造血系统内的各种改变,成为造血障碍的一系列危险因素,包括克隆性造血、免疫衰老、骨髓增殖性肿瘤和白血病。新兴的单细胞技术为造血系统中与年龄相关的变化提供了新的见解。在这篇综述中,我们总结了最近使用单细胞技术剖析造血系统衰老的研究。我们在基因组学、转录组学、表观基因组学、蛋白质组学、代谢组学和空间多组学水平上讨论造血系统衰老过程中发生的细胞变化。最后,我们展望了单细胞技术的未来前景,强调了它们可能给造血系统衰老研究领域带来的影响。

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