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去分化、转分化和重编程:三种再生途径。

Dedifferentiation, transdifferentiation and reprogramming: three routes to regeneration.

机构信息

Center of Regenerative Medicine in Barcelona, Dr. Aiguader, 88, 08003 Barcelona, Spain.

出版信息

Nat Rev Mol Cell Biol. 2011 Feb;12(2):79-89. doi: 10.1038/nrm3043.

DOI:10.1038/nrm3043
PMID:21252997
Abstract

The ultimate goal of regenerative medicine is to replace lost or damaged cells. This can potentially be accomplished using the processes of dedifferentiation, transdifferentiation or reprogramming. Recent advances have shown that the addition of a group of genes can not only restore pluripotency in a fully differentiated cell state (reprogramming) but can also induce the cell to proliferate (dedifferentiation) or even switch to another cell type (transdifferentiation). Current research aims to understand how these processes work and to eventually harness them for use in regenerative medicine.

摘要

再生医学的最终目标是替换丢失或损坏的细胞。这可以通过去分化、转分化或重编程等过程来实现。最近的进展表明,添加一组基因不仅可以恢复完全分化的细胞状态的多能性(重编程),还可以诱导细胞增殖(去分化)甚至转分化为另一种细胞类型。目前的研究旨在了解这些过程是如何工作的,并最终将其用于再生医学。

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Dedifferentiation, transdifferentiation and reprogramming: three routes to regeneration.去分化、转分化和重编程:三种再生途径。
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本文引用的文献

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Advances in understanding tissue regenerative capacity and mechanisms in animals.动物组织再生能力和机制的研究进展。
Nat Rev Genet. 2010 Oct;11(10):710-22. doi: 10.1038/nrg2879. Epub 2010 Sep 14.
2
Direct reprogramming of fibroblasts into functional cardiomyocytes by defined factors.通过定义因子将成纤维细胞直接重编程为功能性心肌细胞。
Cell. 2010 Aug 6;142(3):375-86. doi: 10.1016/j.cell.2010.07.002.
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Transient inactivation of Rb and ARF yields regenerative cells from postmitotic mammalian muscle.Rb 和 ARF 的瞬时失活可从有丝分裂后哺乳动物肌肉中产生再生细胞。
Cell Res. 2025 Jul 8. doi: 10.1038/s41422-025-01138-z.
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The drug-elicitable alternative splicing module for tunable vector expression in the heart.用于心脏中可调载体表达的药物诱导性可变剪接模块。
Nat Cardiovasc Res. 2025 Jun 13. doi: 10.1038/s44161-025-00665-7.
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Proteomic profiling of small extracellular vesicles from bovine nucleus pulposus cells.牛髓核细胞小细胞外囊泡的蛋白质组学分析
PLoS One. 2025 May 29;20(5):e0324179. doi: 10.1371/journal.pone.0324179. eCollection 2025.
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PSMG2 role in tumorigenesis and stemness mediated by protein accumulation, reticulum stress and autophagy.PSMG2在由蛋白质积累、内质网应激和自噬介导的肿瘤发生和干性中的作用。
Int J Biol Sci. 2025 Mar 21;21(6):2531-2549. doi: 10.7150/ijbs.105263. eCollection 2025.
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Cell Reprogramming, Transdifferentiation, and Dedifferentiation Approaches for Heart Repair.用于心脏修复的细胞重编程、转分化和去分化方法。
Int J Mol Sci. 2025 Mar 27;26(7):3063. doi: 10.3390/ijms26073063.
8
Mesangiogenic progenitor cells: a mesengenic and vasculogenic branch of hemopoiesis? A story of neglected plasticity.系膜生成祖细胞:造血的一个中胚层生成和血管生成分支?一个被忽视的可塑性故事。
Front Cell Dev Biol. 2025 Mar 24;13:1513440. doi: 10.3389/fcell.2025.1513440. eCollection 2025.
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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.
10
Transdifferentiation of plasmatocytes to crystal cells in the lymph gland of Drosophila melanogaster.黑腹果蝇淋巴腺中浆血细胞向晶细胞的转分化。
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Cell Stem Cell. 2010 Aug 6;7(2):198-213. doi: 10.1016/j.stem.2010.05.022.
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Epigenetic memory in induced pluripotent stem cells.诱导多能干细胞中的表观遗传记忆。
Nature. 2010 Sep 16;467(7313):285-90. doi: 10.1038/nature09342.
5
Schwann cell dedifferentiation is independent of mitogenic signaling and uncoupled to proliferation: role of cAMP and JNK in the maintenance of the differentiated state.施万细胞去分化独立于有丝分裂信号,并且与增殖解耦:cAMP 和 JNK 在维持分化状态中的作用。
J Biol Chem. 2010 Oct 1;285(40):31024-36. doi: 10.1074/jbc.M110.116970. Epub 2010 Jul 15.
6
Nuclear reprogramming to a pluripotent state by three approaches.三种方法实现细胞核重编程为多能性状态。
Nature. 2010 Jun 10;465(7299):704-12. doi: 10.1038/nature09229.
7
Emerging roles of microRNAs in the control of embryonic stem cells and the generation of induced pluripotent stem cells.微小 RNA 在胚胎干细胞调控和诱导多能干细胞生成中的新兴作用。
Dev Biol. 2010 Aug 1;344(1):16-25. doi: 10.1016/j.ydbio.2010.05.014. Epub 2010 May 15.
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Dynamic single-cell imaging of direct reprogramming reveals an early specifying event.动态单细胞成像直接重编程揭示早期指定事件。
Nat Biotechnol. 2010 May;28(5):521-6. doi: 10.1038/nbt.1632. Epub 2010 May 2.
9
Combined inactivation of pRB and hippo pathways induces dedifferentiation in the Drosophila retina.联合抑制 pRB 和 hippo 通路可诱导果蝇视网膜去分化。
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Conversion of adult pancreatic alpha-cells to beta-cells after extreme beta-cell loss.成年胰腺α细胞在β细胞大量缺失后向β细胞的转化。
Nature. 2010 Apr 22;464(7292):1149-54. doi: 10.1038/nature08894. Epub 2010 Apr 4.