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干细胞功能和维持——至关重要的末端:端粒和端粒酶的作用。

Stem cell function and maintenance - ends that matter: role of telomeres and telomerase.

机构信息

Department of Endocrinology, School of Medicine, Stanford University, Stanford, CA, USA.

出版信息

J Biosci. 2013 Sep;38(3):641-9. doi: 10.1007/s12038-013-9346-3.

DOI:10.1007/s12038-013-9346-3
PMID:23938394
Abstract

Stem cell research holds a promise to treat and prevent age-related degenerative changes in humans. Literature is replete with studies showing that stem cell function declines with aging, especially in highly proliferative tissues/ organs. Among others, telomerase and telomere damage is one of the intrinsic physical instigators that drive agerelated degenerative changes. In this review we provide brief overview of telomerase-deficient aging affects in diverse stem cells populations. Furthermore, potential disease phenotypes associated with telomerase dysregulation in a specific stem cell population is also discussed in this review. Additionally, the role of telomerase in stem cell driven cancer is also briefly touched upon.

摘要

干细胞研究有望治疗和预防人类与年龄相关的退行性变化。文献中充满了研究表明,随着年龄的增长,干细胞功能下降,尤其是在高度增殖的组织/器官中。其中,端粒酶和端粒损伤是导致与年龄相关的退行性变化的内在物理诱因之一。在这篇综述中,我们简要概述了端粒酶缺陷性衰老对不同干细胞群体的影响。此外,还讨论了特定干细胞群体中端粒酶失调与潜在疾病表型的关系。此外,还简要探讨了端粒酶在干细胞驱动的癌症中的作用。

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本文引用的文献

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Mechanisms underlying the osteo- and adipo-differentiation of human mesenchymal stem cells.人骨髓间充质干细胞成骨与成脂分化的潜在机制。
ScientificWorldJournal. 2012;2012:793823. doi: 10.1100/2012/793823. Epub 2012 Mar 12.
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Human blood-vessel-derived stem cells for tissue repair and regeneration.用于组织修复和再生的人血管源性干细胞。
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Age-related cognitive decline: can neural stem cells help us?年龄相关性认知衰退:神经干细胞能帮助我们吗?
在静止的裂殖酵母细胞中,通过端粒序列的重复,磨损的端粒发生重排。
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Stem cells in degenerative orthopaedic pathologies: effects of aging on therapeutic potential.退行性骨科疾病中的干细胞:衰老对治疗潜力的影响。
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Adult stem cell and mesenchymal progenitor theories of aging.衰老的成体干细胞和间充质祖细胞理论。
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Telomere shortening reduces Alzheimer's disease amyloid pathology in mice.端粒缩短可减少小鼠阿尔茨海默病淀粉样蛋白病理。
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5
Telomerase-deficient mice exhibit bone loss owing to defects in osteoblasts and increased osteoclastogenesis by inflammatory microenvironment.端粒酶缺陷小鼠由于成骨细胞缺陷和炎症微环境导致破骨细胞生成增加而出现骨质流失。
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6
Telomerase reactivation reverses tissue degeneration in aged telomerase-deficient mice.端粒酶重新激活可逆转端粒酶缺陷型老年小鼠的组织退化。
Nature. 2011 Jan 6;469(7328):102-6. doi: 10.1038/nature09603. Epub 2010 Nov 28.
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Linking functional decline of telomeres, mitochondria and stem cells during ageing.衰老过程中端粒、线粒体和干细胞功能下降的关联。
Nature. 2010 Mar 25;464(7288):520-8. doi: 10.1038/nature08982.
8
Hemato-vascular origins of endothelial progenitor cells?内皮祖细胞的血液血管起源?
Microvasc Res. 2010 May;79(3):169-73. doi: 10.1016/j.mvr.2010.02.003. Epub 2010 Feb 10.
9
Alterations of the systemic environment are the primary cause of impaired B and T lymphopoiesis in telomere-dysfunctional mice.系统性环境的改变是端粒功能障碍小鼠中 B 和 T 淋巴发生受损的主要原因。
Blood. 2010 Feb 25;115(8):1481-9. doi: 10.1182/blood-2009-08-237230. Epub 2009 Dec 2.
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Telomere shortening in neural stem cells disrupts neuronal differentiation and neuritogenesis.神经干细胞中的端粒缩短会破坏神经元分化和神经突形成。
J Neurosci. 2009 Nov 18;29(46):14394-407. doi: 10.1523/JNEUROSCI.3836-09.2009.