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对造血干细胞衰老的原因、后果及纠正的新见解。

New insight into the causes, consequences, and correction of hematopoietic stem cell aging.

作者信息

Mansell Els, Lin Dawn S, Loughran Stephen J, Milsom Michael D, Trowbridge Jennifer J

机构信息

Erasmus MC Hematology, Rotterdam, The Netherlands; Division of Molecular Medicine and Gene Therapy, Lund University, Lund, Sweden.

Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM), Heidelberg, Germany; Division of Stem Cells and Cancer, German Cancer Research Center (DKFZ), Heidelberg, Germany.

出版信息

Exp Hematol. 2023 Sep-Oct;125-126:1-5. doi: 10.1016/j.exphem.2023.07.002. Epub 2023 Jul 9.

Abstract

Aging of hematopoietic stem cells (HSCs) is characterized by lineage bias, increased clonal expansion, and functional decrease. At the molecular level, aged HSCs typically display metabolic dysregulation, upregulation of inflammatory pathways, and downregulation of DNA repair pathways. Cellular aging of HSCs, driven by cell-intrinsic and cell-extrinsic factors, causes a predisposition to anemia, adaptive immune compromise, myelodys, plasia, and malignancy. Most hematologic diseases are strongly associated with age. But what is the biological foundation for decreased fitness with age? And are there therapeutic windows to resolve age-related hematopoietic decline? These questions were the focus of the International Society for Experimental Hematology (ISEH) New Investigator Committee Fall 2022 Webinar. This review touches on the latest insights from two leading laboratories into inflammatory- and niche-driven stem cell aging and includes speculation on strategies to prevent or correct age-related decline in HSC function.

摘要

造血干细胞(HSCs)的衰老特征为谱系偏向、克隆扩增增加和功能下降。在分子水平上,衰老的造血干细胞通常表现出代谢失调、炎症途径上调和DNA修复途径下调。由细胞内在和外在因素驱动的造血干细胞的细胞衰老会导致易患贫血、适应性免疫受损、骨髓发育异常、发育异常和恶性肿瘤。大多数血液疾病都与年龄密切相关。但是,随着年龄增长健康状况下降的生物学基础是什么?是否存在解决与年龄相关的造血功能衰退的治疗窗口期?这些问题是国际实验血液学学会(ISEH)新研究员委员会2022年秋季网络研讨会的重点。本综述涉及两个领先实验室对炎症和微环境驱动的干细胞衰老的最新见解,并包括对预防或纠正造血干细胞功能与年龄相关衰退的策略的推测。

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