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造血干细胞的栖息地:骨髓龛。

Where Hematopoietic Stem Cells Live: The Bone Marrow Niche.

机构信息

1 Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine , Stanford, California.

2 Department of Medical Biotechnology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University , Krakow, Poland .

出版信息

Antioxid Redox Signal. 2018 Jul 10;29(2):191-204. doi: 10.1089/ars.2017.7419. Epub 2018 Jan 9.

Abstract

Hematopoietic stem cells (HSCs) can sustain the production of blood throughout one's lifetime. However, for proper self-renewal of its own population and differentiation to blood, the HSC requires a specialized microenvironment called the "niche." Recent Advances: Recent studies using novel mouse models have shed new light on the cellular architecture and function of the HSC niche. Here, we review the different cells that constitute the HSC niche and the molecular mechanisms that underlie HSC and niche interaction. We discuss the evidence and potential features that distinguish the HSC niche from other microenvironments in the bone marrow. The relevance of the niche in malignant transformation of the HSCs and harboring cancer metastasis to the bone is also outlined. In addition, we address how the niche may regulate reactive oxygen species levels surrounding the HSCs. Critical Issues and Future Directions: We propose future directions and remaining challenges in investigating the niche of HSCs. We discuss how a better understanding of the HSC niche may help in restoring an aged hematopoietic system, fighting against malignancies, and transplanting purified HSCs safely and effectively into patients. Antioxid. Redox Signal. 00, 000-000.

摘要

造血干细胞(HSCs)可以在人的一生当中持续产生血液。然而,为了实现其自身群体的适当自我更新和向血液的分化,HSC 需要一个称为“龛”的专门微环境。最新进展:最近使用新型小鼠模型的研究揭示了 HSC 龛的细胞结构和功能的新见解。在这里,我们回顾了构成 HSC 龛的不同细胞以及HSC 和龛相互作用的分子机制。我们讨论了区分 HSC 龛与骨髓中其他微环境的证据和潜在特征。HSC 龛在恶性转化和癌症转移到骨骼中的相关性也进行了概述。此外,我们还探讨了龛如何调节围绕 HSCs 的活性氧水平。关键问题和未来方向:我们提出了研究 HSCs 龛的未来方向和遗留挑战。我们讨论了更好地了解 HSC 龛如何有助于恢复衰老的造血系统、对抗恶性肿瘤以及安全有效地将纯化的 HSCs 移植到患者体内。抗氧化。氧化还原信号。00,000-000。

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