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造血干细胞命运调控与恶性肿瘤

Regulation of Hematopoietic Stem Cell Fate and Malignancy.

机构信息

Immunotherapy Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 125 Gwahak-ro, Yuseong-gu, Daejeon 34141, Korea.

Environmental Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 125 Gwahak-ro, Yuseong-gu, Daejeon 34141, Korea.

出版信息

Int J Mol Sci. 2020 Jul 6;21(13):4780. doi: 10.3390/ijms21134780.

Abstract

The regulation of hematopoietic stem cell (HSC) fate decision, whether they keep quiescence, self-renew, or differentiate into blood lineage cells, is critical for maintaining the immune system throughout one's lifetime. As HSCs are exposed to age-related stress, they gradually lose their self-renewal and regenerative capacity. Recently, many reports have implicated signaling pathways in the regulation of HSC fate determination and malignancies under aging stress or pathophysiological conditions. In this review, we focus on the current understanding of signaling pathways that regulate HSC fate including quiescence, self-renewal, and differentiation during aging, and additionally introduce pharmacological approaches to rescue defects of HSC fate determination or hematopoietic malignancies by kinase signaling pathways.

摘要

造血干细胞(HSC)命运决策的调节,无论是保持静止、自我更新还是分化为血液谱系细胞,对于维持整个生命周期的免疫系统都至关重要。随着 HSC 暴露于与年龄相关的应激下,它们逐渐失去自我更新和再生能力。最近,许多报告表明,在衰老应激或病理生理条件下,信号通路参与调节 HSC 命运决定和恶性肿瘤。在这篇综述中,我们重点介绍了调节 HSC 命运的信号通路的最新认识,包括衰老过程中 HSC 的静止、自我更新和分化,并介绍了通过激酶信号通路拯救 HSC 命运决定或造血恶性肿瘤缺陷的药理学方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d78/7369689/1644e897cb21/ijms-21-04780-g001.jpg

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