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细胞重编程过程中的染色质动力学。

Chromatin dynamics during cellular reprogramming.

机构信息

1] Massachusetts General Hospital Center for Regenerative Medicine, 185 Cambridge Street, Boston, Massachusetts 02114, USA. [2] Harvard Stem Cell Institute, 1350 Masschusetts Avenue, Cambridge, Massachusetts 02138, USA. [3] Howard Hughes Medical Institute, 4000 Jones Bridge Road, Chevy Chase, Maryland 20815, USA. [4] Department of Stem Cell and Regenerative Biology, Harvard University and Harvard Medical School, 7 Divinity Avenue, Cambridge, Massachusetts 02138, USA.

出版信息

Nature. 2013 Oct 24;502(7472):462-71. doi: 10.1038/nature12749.

DOI:10.1038/nature12749
PMID:24153299
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4216318/
Abstract

Induced pluripotency is a powerful tool to derive patient-specific stem cells. In addition, it provides a unique assay to study the interplay between transcription factors and chromatin structure. Here, we review the latest insights into chromatin dynamics that are inherent to induced pluripotency. Moreover, we compare and contrast these events with other physiological and pathological processes that involve changes in chromatin and cell state, including germ cell maturation and tumorigenesis. We propose that an integrated view of these seemingly diverse processes could provide mechanistic insights into cell fate transitions in general and might lead to new approaches in regenerative medicine and cancer treatment.

摘要

诱导多能性是一种强大的工具,可以衍生出患者特异性的干细胞。此外,它提供了一种独特的检测方法,用于研究转录因子和染色质结构之间的相互作用。在这里,我们回顾了与诱导多能性相关的染色质动力学的最新见解。此外,我们将这些事件与其他涉及染色质和细胞状态变化的生理和病理过程进行了比较和对比,包括生殖细胞成熟和肿瘤发生。我们提出,对这些看似不同的过程进行综合观察,可以为细胞命运转变提供机制上的见解,并可能为再生医学和癌症治疗带来新的方法。

相似文献

1
Chromatin dynamics during cellular reprogramming.细胞重编程过程中的染色质动力学。
Nature. 2013 Oct 24;502(7472):462-71. doi: 10.1038/nature12749.
2
Epigenetics of cellular reprogramming.细胞重编程的表观遗传学。
Curr Opin Genet Dev. 2013 Oct;23(5):548-55. doi: 10.1016/j.gde.2013.06.005. Epub 2013 Aug 12.
3
Mechanisms of nuclear reprogramming by eggs and oocytes: a deterministic process?卵母细胞和卵子重编程核的机制:一个确定性过程?
Nat Rev Mol Cell Biol. 2011 Jun 23;12(7):453-9. doi: 10.1038/nrm3140.
4
Reprogramming chromatin.重编程染色质。
Crit Rev Biochem Mol Biol. 2012 Sep;47(5):464-82. doi: 10.3109/10409238.2012.697125. Epub 2012 Jul 3.
5
Generation of human induced pluripotent stem cells using epigenetic regulators reveals a germ cell-like identity in partially reprogrammed colonies.利用表观遗传调节剂生成人类诱导多能干细胞揭示了部分重编程集落中具有生殖细胞样的特性。
PLoS One. 2013 Dec 12;8(12):e82838. doi: 10.1371/journal.pone.0082838. eCollection 2013.
6
Epigenetics of reprogramming to induced pluripotency.重编程为诱导多能性的表观遗传学。
Cell. 2013 Mar 14;152(6):1324-43. doi: 10.1016/j.cell.2013.02.043.
7
Reprogramming of cell fate: epigenetic memory and the erasure of memories past.细胞命运重编程:表观遗传记忆与过往记忆的消除
EMBO J. 2015 May 12;34(10):1296-308. doi: 10.15252/embj.201490649. Epub 2015 Mar 27.
8
The role of the reprogramming method and pluripotency state in gamete differentiation from patient-specific human pluripotent stem cells.重编程方法和多能性状态在患者特异性人多能干细胞向配子分化中的作用。
Mol Hum Reprod. 2018 Apr 1;24(4):173-184. doi: 10.1093/molehr/gay007.
9
Resetting epigenetic signatures to induce somatic cell reprogramming.重置表观遗传特征以诱导体细胞重编程。
Cell Mol Life Sci. 2013 Apr;70(8):1413-24. doi: 10.1007/s00018-012-1137-8. Epub 2012 Aug 30.
10
Reprogramming factor expression initiates widespread targeted chromatin remodeling.重编程因子表达引发广泛的靶向染色质重塑。
Cell Stem Cell. 2011 Jan 7;8(1):96-105. doi: 10.1016/j.stem.2010.12.001.

引用本文的文献

1
Engineered extracellular vesicles derived from pluripotent stem cells: a cell-free approach to regenerative medicine.源自多能干细胞的工程化细胞外囊泡:再生医学的无细胞方法
Burns Trauma. 2025 Feb 11;13:tkaf013. doi: 10.1093/burnst/tkaf013. eCollection 2025.
2
The role of PSMC4 in non-small cell lung cancer: implications for prognosis, diagnosis, and immune microenvironment modulation.PSMC4在非小细胞肺癌中的作用:对预后、诊断及免疫微环境调节的意义
Front Oncol. 2025 May 2;15:1503466. doi: 10.3389/fonc.2025.1503466. eCollection 2025.
3
Molecular basis of cell fate plasticity - insights from the privileged cells.

本文引用的文献

1
Topology of mammalian developmental enhancers and their regulatory landscapes.哺乳动物发育增强子的拓扑结构及其调控景观。
Nature. 2013 Oct 24;502(7472):499-506. doi: 10.1038/nature12753.
2
Establishment of totipotency does not depend on Oct4A.全能性的建立并不依赖于 Oct4A。
Nat Cell Biol. 2013 Sep;15(9):1089-97. doi: 10.1038/ncb2816. Epub 2013 Aug 11.
3
Pluripotent stem cells induced from mouse somatic cells by small-molecule compounds.小分子化合物诱导的小鼠体细胞多能干细胞。
细胞命运可塑性的分子基础——来自特权细胞的见解
Curr Opin Genet Dev. 2025 Aug;93:102354. doi: 10.1016/j.gde.2025.102354. Epub 2025 May 5.
4
Cell reprogramming: methods, mechanisms and applications.细胞重编程:方法、机制与应用
Cell Regen. 2025 Mar 27;14(1):12. doi: 10.1186/s13619-025-00229-x.
5
Ultrasound-triggered three dimensional hyaluronic acid hydrogel promotes in vitro and in vivo reprogramming into induced pluripotent stem cells.超声触发的三维透明质酸水凝胶促进体外和体内重编程为诱导多能干细胞。
Bioact Mater. 2024 May 9;38:331-345. doi: 10.1016/j.bioactmat.2024.05.011. eCollection 2024 Aug.
6
Multiscale chromatin dynamics and high entropy in plant iPSC ancestors.植物 iPSC 祖先中的多尺度染色质动力学和高熵。
J Cell Sci. 2024 Oct 15;137(20). doi: 10.1242/jcs.261703. Epub 2024 Jun 24.
7
Induced pluripotent stem cells (iPSCs): molecular mechanisms of induction and applications.诱导多能干细胞(iPSCs):诱导的分子机制与应用。
Signal Transduct Target Ther. 2024 Apr 26;9(1):112. doi: 10.1038/s41392-024-01809-0.
8
Unlocking the Potential of Induced Pluripotent Stem Cells in Revolutionizing Cancer Therapy.释放诱导多能干细胞在革新癌症治疗方面的潜力。
Curr Stem Cell Res Ther. 2025;20(4):360-376. doi: 10.2174/011574888X294791240408055222.
9
Metabolic control of induced pluripotency.诱导多能性的代谢调控。
Front Cell Dev Biol. 2024 Jan 11;11:1328522. doi: 10.3389/fcell.2023.1328522. eCollection 2023.
10
The thyroid hormone enhances mouse embryonic fibroblasts reprogramming to pluripotent stem cells: role of the nuclear receptor corepressor 1.甲状腺激素增强小鼠胚胎成纤维细胞重编程为多能干细胞:核受体共抑制因子 1 的作用。
Front Endocrinol (Lausanne). 2023 Dec 1;14:1235614. doi: 10.3389/fendo.2023.1235614. eCollection 2023.
Science. 2013 Aug 9;341(6146):651-4. doi: 10.1126/science.1239278. Epub 2013 Jul 18.
4
Maturation, not initiation, is the major roadblock during reprogramming toward pluripotency from human fibroblasts.在将人成纤维细胞重编程为多能性的过程中,成熟而不是起始是主要的障碍。
Proc Natl Acad Sci U S A. 2013 Jul 23;110(30):12172-9. doi: 10.1073/pnas.1310291110. Epub 2013 Jun 28.
5
Vitamin C induces Tet-dependent DNA demethylation and a blastocyst-like state in ES cells.维生素 C 诱导胚胎干细胞中的 Tet 依赖性 DNA 去甲基化和类囊胚状态。
Nature. 2013 Aug 8;500(7461):222-6. doi: 10.1038/nature12362. Epub 2013 Jun 30.
6
Stage-specific regulation of reprogramming to induced pluripotent stem cells by Wnt signaling and T cell factor proteins.Wnt 信号和 T 细胞因子蛋白对重编程为诱导多能干细胞的阶段特异性调控。
Cell Rep. 2013 Jun 27;3(6):2113-26. doi: 10.1016/j.celrep.2013.05.015. Epub 2013 Jun 20.
7
Proteomic and genomic approaches reveal critical functions of H3K9 methylation and heterochromatin protein-1γ in reprogramming to pluripotency.蛋白质组学和基因组学方法揭示了 H3K9 甲基化和异染色质蛋白-1γ在重编程为多能性中的关键功能。
Nat Cell Biol. 2013 Jul;15(7):872-82. doi: 10.1038/ncb2768. Epub 2013 Jun 9.
8
Klf4 organizes long-range chromosomal interactions with the oct4 locus in reprogramming and pluripotency.Klf4 在重编程和多能性中与 oct4 基因座组织长距离染色体相互作用。
Cell Stem Cell. 2013 Jul 3;13(1):36-47. doi: 10.1016/j.stem.2013.05.010. Epub 2013 Jun 6.
9
Intrachromosomal looping is required for activation of endogenous pluripotency genes during reprogramming.染色体内环化是重编程过程中激活内源性多能性基因所必需的。
Cell Stem Cell. 2013 Jul 3;13(1):30-5. doi: 10.1016/j.stem.2013.05.012. Epub 2013 Jun 6.
10
High-resolution analysis with novel cell-surface markers identifies routes to iPS cells.高分辨率分析新型细胞表面标志物鉴定 iPS 细胞的途径。
Nature. 2013 Jul 4;499(7456):88-91. doi: 10.1038/nature12243. Epub 2013 Jun 2.