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本文引用的文献

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Altered microenvironmental regulation of leukemic and normal stem cells in chronic myelogenous leukemia.慢性髓性白血病中白血病和正常干细胞的微环境调节改变。
Cancer Cell. 2012 Apr 17;21(4):577-92. doi: 10.1016/j.ccr.2012.02.018.
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Synergistic, context-dependent, and hierarchical functions of epithelial components in thymic microenvironments.胸腺微环境中上皮细胞成分的协同、上下文相关和层次功能。
Cell. 2012 Mar 30;149(1):159-72. doi: 10.1016/j.cell.2012.01.049.
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N-cadherin in osteolineage cells is not required for maintenance of hematopoietic stem cells.骨细胞系中的 N-钙黏蛋白对于维持造血干细胞并非必需。
Blood. 2012 Jul 12;120(2):295-302. doi: 10.1182/blood-2011-09-377457. Epub 2012 Feb 9.
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Endothelial and perivascular cells maintain haematopoietic stem cells.内皮细胞和血管周细胞维持造血干细胞。
Nature. 2012 Jan 25;481(7382):457-62. doi: 10.1038/nature10783.
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Extramedullary hematopoiesis: a new look at the underlying stem cell niche, theories of development, and occurrence in animals.髓外造血:对基础造血干细胞龛、发育理论以及动物发生的新认识。
Vet Pathol. 2012 May;49(3):508-23. doi: 10.1177/0300985811432344. Epub 2012 Jan 18.
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Interaction between differentiating cell- and niche-derived signals in hematopoietic progenitor maintenance.造血祖细胞维持中分化细胞和龛来源信号的相互作用。
Cell. 2011 Dec 23;147(7):1589-600. doi: 10.1016/j.cell.2011.11.041.
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Rac signaling in osteoblastic cells is required for normal bone development but is dispensable for hematopoietic development.Rac 信号在成骨细胞中对于正常骨发育是必需的,但对于造血发育是可有可无的。
Blood. 2012 Jan 19;119(3):736-44. doi: 10.1182/blood-2011-07-368753. Epub 2011 Nov 28.
8
Stromal-derived factor-1 and its receptor, CXCR4, are constitutively expressed by mouse liver sinusoidal endothelial cells: implications for the regulation of hematopoietic cell migration to the liver during extramedullary hematopoiesis.基质衍生因子-1 及其受体 CXCR4 持续表达于小鼠肝窦内皮细胞:对骨髓外造血过程中造血细胞向肝脏迁移的调控意义。
Stem Cells Dev. 2012 Aug 10;21(12):2142-51. doi: 10.1089/scd.2011.0565. Epub 2012 Jan 26.
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Nonmyelinating Schwann cells maintain hematopoietic stem cell hibernation in the bone marrow niche.无髓鞘施万细胞维持骨髓龛中造血干细胞的休眠状态。
Cell. 2011 Nov 23;147(5):1146-58. doi: 10.1016/j.cell.2011.09.053.
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Integrin-αvβ3 regulates thrombopoietin-mediated maintenance of hematopoietic stem cells.整合素-αvβ3 调节血小板生成素介导的造血干细胞维持。
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龛对正常和白血病造血干细胞的调控。

The regulation of normal and leukemic hematopoietic stem cells by niches.

作者信息

Huang Meng-Meng, Zhu Jiang

机构信息

State Key Laboratory for Medical Genomics and Shanghai Institute of Hematology, Rui-Jin Hospital, Shanghai Jiao-Tong University School of Medicine, Shanghai, 200025, People's Republic of China.

出版信息

Cancer Microenviron. 2012 Dec;5(3):295-305. doi: 10.1007/s12307-012-0114-y. Epub 2012 Jul 22.

DOI:10.1007/s12307-012-0114-y
PMID:23055016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3460044/
Abstract

The origin and propagation of normal and leukemic hematopoietic cells critically depend on their interplays with the hematopoietic microenvironment (or so-called niche), which represent important biological models for understanding organogenesis and tumorigenesis. Nevertheless, the anatomic and functional characterizations of the niche cells for normal hematopoietic stem cells (HSCs) have proved a formidable task. It is uncertain whether the combinational effects of a few sets of molecular niche elements, behind the long-sought cellular architectures with preferred anatomic locations, actually meets the functional definition of HSC niche. Moreover, even much less is known about the niche components for numerous types of leukemia-stem cells (LSCs) that originate via discrete cellular and molecular transforming mechanisms. However, one interesting scenario is emerging, i.e., the leukemia cells can positively remodel the hematopoietic microenvironment favorable for their competition over the normal hematopoiesis that co-exists within the same eco-system. This property probably represents a previously unappreciated essential trait of a functional LSC. Obviously, the further exploration into how the hematopoietic microenvironment interplay with normal or malignant hematopoiesis will shed light onto the designing of novel types of niche-targeting therapies for leukemia.

摘要

正常造血细胞和白血病造血细胞的起源与增殖严重依赖于它们与造血微环境(即所谓的生态位)的相互作用,造血微环境是理解器官发生和肿瘤发生的重要生物学模型。然而,对正常造血干细胞(HSC)生态位细胞的解剖学和功能特征进行表征已被证明是一项艰巨的任务。目前尚不确定,在长期寻找的具有特定解剖位置的细胞结构背后,几组分子生态位元件的组合效应是否真的符合HSC生态位的功能定义。此外,对于通过离散的细胞和分子转化机制产生的多种类型白血病干细胞(LSC)的生态位组成,人们了解得更少。然而,一个有趣的情况正在出现,即白血病细胞可以积极重塑造血微环境,使其有利于在同一生态系统中与正常造血竞争。这一特性可能代表了功能性LSC以前未被认识到的基本特征。显然,进一步探索造血微环境如何与正常或恶性造血相互作用,将为设计新型的针对白血病的生态位靶向治疗方法提供线索。