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本文引用的文献

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Gata6 promotes hair follicle progenitor cell renewal by genome maintenance during proliferation.Gata6 通过在增殖过程中维持基因组来促进毛囊祖细胞更新。
EMBO J. 2017 Jan 4;36(1):61-78. doi: 10.15252/embj.201694572. Epub 2016 Dec 1.
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Epigenetic Memory Underlies Cell-Autonomous Heterogeneous Behavior of Hematopoietic Stem Cells.表观遗传记忆是造血干细胞细胞自主异质性行为的基础。
Cell. 2016 Nov 17;167(5):1310-1322.e17. doi: 10.1016/j.cell.2016.10.045.
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Hematopoietic Stem Cells Count and Remember Self-Renewal Divisions.造血干细胞计数并记住自我更新分裂。
Cell. 2016 Nov 17;167(5):1296-1309.e10. doi: 10.1016/j.cell.2016.10.022. Epub 2016 Nov 10.
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Hair follicles' transit-amplifying cells govern concurrent dermal adipocyte production through Sonic Hedgehog.毛囊的过渡放大细胞通过音猬因子调控真皮脂肪细胞的同步产生。
Genes Dev. 2016 Oct 15;30(20):2325-2338. doi: 10.1101/gad.285429.116. Epub 2016 Nov 2.
5
MOZ (KAT6A) is essential for the maintenance of classically defined adult hematopoietic stem cells.MOZ(KAT6A)对于维持经典定义的成体造血干细胞是必需的。
Blood. 2016 Nov 10;128(19):2307-2318. doi: 10.1182/blood-2015-10-676072. Epub 2016 Sep 23.
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Hematopoietic Stem Cells Are the Major Source of Multilineage Hematopoiesis in Adult Animals.造血干细胞是成年动物多谱系造血的主要来源。
Immunity. 2016 Sep 20;45(3):597-609. doi: 10.1016/j.immuni.2016.08.007. Epub 2016 Aug 30.
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Proximity-Based Differential Single-Cell Analysis of the Niche to Identify Stem/Progenitor Cell Regulators.基于邻近性的生态位差异单细胞分析以鉴定干细胞/祖细胞调节因子
Cell Stem Cell. 2016 Oct 6;19(4):530-543. doi: 10.1016/j.stem.2016.07.004. Epub 2016 Aug 11.
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Angiogenin Promotes Hematopoietic Regeneration by Dichotomously Regulating Quiescence of Stem and Progenitor Cells.血管生成素通过二分法调节干细胞和祖细胞的静止状态促进造血再生。
Cell. 2016 Aug 11;166(4):894-906. doi: 10.1016/j.cell.2016.06.042.
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Defining the clonal dynamics leading to mouse skin tumour initiation.定义导致小鼠皮肤肿瘤起始的克隆动力学。
Nature. 2016 Aug 18;536(7616):298-303. doi: 10.1038/nature19069. Epub 2016 Jul 8.
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Polycomb-Mediated Repression and Sonic Hedgehog Signaling Interact to Regulate Merkel Cell Specification during Skin Development.多梳介导的基因沉默与音猬因子信号传导相互作用,在皮肤发育过程中调控默克尔细胞的特化。
PLoS Genet. 2016 Jul 14;12(7):e1006151. doi: 10.1371/journal.pgen.1006151. eCollection 2016 Jul.

过渡放大细胞在组织再生和癌症中的新作用。

Emerging roles of transit-amplifying cells in tissue regeneration and cancer.

作者信息

Zhang Bing, Hsu Ya-Chieh

机构信息

Department of Stem Cell and Regenerative Biology, Harvard University and Harvard Stem Cell Institute, Cambridge, MA, USA.

出版信息

Wiley Interdiscip Rev Dev Biol. 2017 Sep;6(5). doi: 10.1002/wdev.282. Epub 2017 Jul 3.

DOI:10.1002/wdev.282
PMID:28670819
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5561490/
Abstract

Most regenerative tissues employ transit-amplifying cells (TACs) that are positioned in between stem cells and differentiated progeny. In a classical hierarchical model, stem cells undergo limited divisions to produce TACs, which then proliferate rapidly to expand the system and produce diverse differentiated cell types. Although TACs are indispensable for generating tissues, they have been largely viewed as a transit point between stem cells and downstream lineages. Studies in the past few years, however, have revealed some fascinating biology and unanticipated functions of TACs. In the hair follicle, recent findings have placed TACs as key players in tissue regeneration by coordinating tissue production, governing stem cell behaviors, and instructing niche remodeling. In the hematopoietic system, rather than being transient, some TACs may participate in long-term hematopoiesis under steady state. Here, we compare and summarize recent discoveries about TACs in the hair follicle and the hematopoietic system. We also discuss how TACs of these two tissues contribute to the formation of cancer. WIREs Dev Biol 2017, 6:e282. doi: 10.1002/wdev.282 For further resources related to this article, please visit the WIREs website.

摘要

大多数再生组织利用位于干细胞和分化后代之间的过渡扩增细胞(TACs)。在经典的层级模型中,干细胞进行有限的分裂以产生TACs,然后TACs迅速增殖以扩展系统并产生多种分化细胞类型。尽管TACs对于组织生成不可或缺,但它们在很大程度上被视为干细胞和下游谱系之间的一个过渡点。然而,过去几年的研究揭示了TACs一些引人入胜的生物学特性和意想不到的功能。在毛囊中,最近的研究结果表明TACs通过协调组织生成、控制干细胞行为和指导微环境重塑,成为组织再生的关键参与者。在造血系统中,一些TACs可能并非短暂存在,而是在稳态下参与长期造血。在此,我们比较并总结了毛囊和造血系统中关于TACs的最新发现。我们还讨论了这两种组织中的TACs如何促进癌症的形成。《WIREs发育生物学》2017年,6:e282。doi:10.1002/wdev.282 有关本文的更多资源,请访问WIREs网站。