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Aneuploidy in stem cells.干细胞中的非整倍体。
World J Stem Cells. 2016 Jun 26;8(6):216-22. doi: 10.4252/wjsc.v8.i6.216.
2
Chromosome microduplication in somatic cells decreases the genetic stability of human reprogrammed somatic cells and results in pluripotent stem cells.体细胞中的染色体微重复会降低人类重编程体细胞的遗传稳定性,并产生多能干细胞。
Sci Rep. 2015 May 12;5:10114. doi: 10.1038/srep10114.
3
An Overview of Direct Somatic Reprogramming: The Ins and Outs of iPSCs.直接体细胞重编程概述:诱导多能干细胞的来龙去脉
Int J Mol Sci. 2016 Jan 21;17(1):141. doi: 10.3390/ijms17010141.
4
Ten years of progress and promise of induced pluripotent stem cells: historical origins, characteristics, mechanisms, limitations, and potential applications.诱导多能干细胞十年的进展与前景:历史起源、特征、机制、局限性及潜在应用
PeerJ. 2018 May 11;6:e4370. doi: 10.7717/peerj.4370. eCollection 2018.
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Engineering personalized neural tissue by combining induced pluripotent stem cells with fibrin scaffolds.通过将诱导多能干细胞与纤维蛋白支架相结合来构建个性化神经组织。
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Induced pluripotent stem cell potential in medicine, specifically focused on reproductive medicine.诱导多能干细胞在医学中的潜力,特别是专注于生殖医学领域。
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Human embryonic stem cells as models for aneuploid chromosomal syndromes.人类胚胎干细胞作为非整倍体染色体综合征模型。
Stem Cells. 2010 Sep;28(9):1530-40. doi: 10.1002/stem.483.
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Induced Pluripotent Stem Cells: A New Frontier for Stem Cells in Dentistry.诱导多能干细胞:牙科干细胞的新前沿。
J Dent Res. 2015 Nov;94(11):1508-15. doi: 10.1177/0022034515599769. Epub 2015 Aug 18.
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Generation of induced pluripotent stem cells from human mesenchymal stem cells of parotid gland origin.从腮腺来源的人间充质干细胞诱导生成诱导多能干细胞。
Am J Transl Res. 2016 Feb 15;8(2):419-32. eCollection 2016.

引用本文的文献

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DNA Damage Responses, the Trump Card of Stem Cells in the Survival Game.DNA 损伤反应:干细胞在生存游戏中的王牌。
Adv Exp Med Biol. 2024;1470:165-188. doi: 10.1007/5584_2023_791.
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Dynamic Features of Chromosomal Instability during Culture of Induced Pluripotent Stem Cells.诱导多能干细胞培养过程中染色体不稳定性的动态特征。
Genes (Basel). 2022 Jun 27;13(7):1157. doi: 10.3390/genes13071157.
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Chromosomal aberrations after induced pluripotent stem cells reprogramming.诱导多能干细胞重编程后的染色体畸变。
Genet Mol Biol. 2021 Sep 3;44(3):e20200147. doi: 10.1590/1678-4685-GMB-2020-0147. eCollection 2021.
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All models are wrong, but some are useful: Establishing standards for stem cell-based embryo models.所有模型都是错误的,但有些是有用的:建立基于干细胞的胚胎模型的标准。
Stem Cell Reports. 2021 May 11;16(5):1117-1141. doi: 10.1016/j.stemcr.2021.03.019.
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Comparison of chromosomal instability of human amniocytes in primary and long-term cultures in AmnioMAX II and DMEM media: A cross-sectional study.在AmnioMAX II和DMEM培养基中对人羊膜细胞原代培养和长期培养的染色体不稳定性进行比较:一项横断面研究。
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Targeting MAD2 modulates stemness and tumorigenesis in human Gastric Cancer cell lines.靶向 MAD2 调节人胃癌细胞系的干性和肿瘤发生。
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Chromosome misalignment is associated with PLK1 activity at cenexin-positive mitotic centrosomes.染色体错位与中心体上 cenexin 阳性有丝分裂中心体的 PLK1 活性有关。
Mol Biol Cell. 2019 Jun 15;30(13):1598-1609. doi: 10.1091/mbc.E18-12-0817. Epub 2019 May 1.

本文引用的文献

1
Assessment of megabase-scale somatic copy number variation using single-cell sequencing.使用单细胞测序评估兆碱基规模的体细胞拷贝数变异
Genome Res. 2016 Mar;26(3):376-84. doi: 10.1101/gr.198937.115. Epub 2016 Jan 15.
2
Emergence of clonal chromosomal alterations during the mesenchymal stromal cell cultivation.间充质基质细胞培养过程中克隆性染色体改变的出现。
Mol Cytogenet. 2015 Dec 1;8:94. doi: 10.1186/s13039-015-0197-5. eCollection 2015.
3
CINcere Modelling: What Have Mouse Models for Chromosome Instability Taught Us?癌症建模:染色体不稳定的小鼠模型给了我们哪些启示?
Recent Results Cancer Res. 2015;200:39-60. doi: 10.1007/978-3-319-20291-4_2.
4
Toward understanding and exploiting tumor heterogeneity.迈向对肿瘤异质性的理解与利用。
Nat Med. 2015 Aug;21(8):846-53. doi: 10.1038/nm.3915.
5
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain.单细胞全基因组测序鉴定出人类大脑中的克隆性体细胞拷贝数变异。
Cell Rep. 2015 Feb 3;10(4):645. doi: 10.1016/j.celrep.2015.01.028.
6
How to count chromosomes in a cell: An overview of current and novel technologies.如何在细胞中计数染色体:当前技术与新技术概述
Bioessays. 2015 May;37(5):570-7. doi: 10.1002/bies.201400218. Epub 2015 Mar 4.
7
Single cell sequencing reveals low levels of aneuploidy across mammalian tissues.单细胞测序揭示了哺乳动物组织中存在低水平的非整倍体现象。
Proc Natl Acad Sci U S A. 2014 Sep 16;111(37):13409-14. doi: 10.1073/pnas.1415287111. Epub 2014 Sep 2.
8
Genetic evaluation of mesenchymal stem cells by G-banded karyotyping in a Cell Technology Center.在一个细胞技术中心通过G带核型分析对间充质干细胞进行基因评估。
Rev Bras Hematol Hemoter. 2014 May-Jun;36(3):202-7. doi: 10.1016/j.bjhh.2014.03.006. Epub 2014 Apr 3.
9
Aneuploidy in pluripotent stem cells and implications for cancerous transformation.多能干细胞中的非整倍体及其对癌变的影响。
Protein Cell. 2014;5(8):569-79. doi: 10.1007/s13238-014-0073-9. Epub 2014 Jun 5.
10
Genetic and epigenetic instability of stem cells.干细胞的遗传与表观遗传不稳定性。
Cell Transplant. 2014;23(4-5):417-33. doi: 10.3727/096368914X678472. Epub 2014 Mar 11.

干细胞中的非整倍体。

Aneuploidy in stem cells.

作者信息

Garcia-Martinez Jorge, Bakker Bjorn, Schukken Klaske M, Simon Judith E, Foijer Floris

机构信息

Jorge Garcia-Martinez, Bjorn Bakker, Klaske M Schukken, Judith E Simon, Floris Foijer, European Research Institute for the Biology of Ageing, University of Groningen, University Medical Center Groningen, NL-9713 AV Groningen, The Netherlands.

出版信息

World J Stem Cells. 2016 Jun 26;8(6):216-22. doi: 10.4252/wjsc.v8.i6.216.

DOI:10.4252/wjsc.v8.i6.216
PMID:27354891
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4919689/
Abstract

Stem cells hold enormous promise for regenerative medicine as well as for engineering of model systems to study diseases and develop new drugs. The discovery of protocols that allow for generating induced pluripotent stem cells (IPSCs) from somatic cells has brought this promise steps closer to reality. However, as somatic cells might have accumulated various chromosomal abnormalities, including aneuploidies throughout their lives, the resulting IPSCs might no longer carry the perfect blueprint for the tissue to be generated, or worse, become at risk of adopting a malignant fate. In this review, we discuss the contribution of aneuploidy to healthy tissues and how aneuploidy can lead to disease. Furthermore, we review the differences between how somatic cells and stem cells respond to aneuploidy.

摘要

干细胞在再生医学以及用于研究疾病和开发新药的模型系统工程方面具有巨大的潜力。能够从体细胞生成诱导多能干细胞(iPSC)的方案的发现,使这一前景更接近现实。然而,由于体细胞在其整个生命过程中可能积累了各种染色体异常,包括非整倍体,由此产生的iPSC可能不再携带生成组织的完美蓝图,或者更糟的是,有发生恶性病变的风险。在这篇综述中,我们讨论了非整倍体对健康组织的影响以及非整倍体如何导致疾病。此外,我们还综述了体细胞和干细胞对非整倍体反应的差异。