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迫使细胞改变谱系。

Forcing cells to change lineages.

作者信息

Graf Thomas, Enver Tariq

机构信息

Center for Genomic Regulation and ICREA, 08003 Barcelona, Spain.

出版信息

Nature. 2009 Dec 3;462(7273):587-94. doi: 10.1038/nature08533.

DOI:10.1038/nature08533
PMID:19956253
Abstract

The ability to produce stem cells by induced pluripotency (iPS reprogramming) has rekindled an interest in earlier studies showing that transcription factors can directly convert specialized cells from one lineage to another. Lineage reprogramming has become a powerful tool to study cell fate choice during differentiation, akin to inducing mutations for the discovery of gene functions. The lessons learnt provide a rubric for how cells may be manipulated for therapeutic purposes.

摘要

通过诱导多能性产生干细胞的能力(iPS重编程)重新唤起了人们对早期研究的兴趣,这些研究表明转录因子可以直接将一种谱系的特化细胞转化为另一种谱系的细胞。谱系重编程已成为研究分化过程中细胞命运选择的有力工具,类似于为发现基因功能而诱导突变。所学到的经验教训为如何出于治疗目的操纵细胞提供了一个准则。

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Pax3:Foxc2 reciprocal repression in the somite modulates muscular versus vascular cell fate choice in multipotent progenitors.Pax3:Foxc2 相互抑制在体节中调节多能祖细胞中的肌肉与血管细胞命运选择。
Dev Cell. 2009 Dec;17(6):892-9. doi: 10.1016/j.devcel.2009.10.021.
2
MafB restricts M-CSF-dependent myeloid commitment divisions of hematopoietic stem cells.MafB限制造血干细胞中依赖巨噬细胞集落刺激因子(M-CSF)的髓系定向分化分裂。
Cell. 2009 Jul 23;138(2):300-13. doi: 10.1016/j.cell.2009.04.057.
3
Hematopoietic cytokines can instruct lineage choice.
组蛋白变体:细胞去分化和转分化过程中炎症的关键调节因子。
Front Immunol. 2025 Jun 27;16:1619100. doi: 10.3389/fimmu.2025.1619100. eCollection 2025.
4
Excitation-inhibition balance abnormally shapes structure-function coupling of gray matter in Parkinson's disease.兴奋-抑制平衡异常塑造了帕金森病中灰质的结构-功能耦合。
NPJ Parkinsons Dis. 2025 Jun 13;11(1):168. doi: 10.1038/s41531-025-01028-6.
5
Optimizing single cell RNA sequencing of stem cells. A streamlined workflow for enhanced sensitivity and reproducibility in hematopoietic studies. The use of human umbilical cord blood-derived hematopoietic stem and progenitor cells.优化干细胞的单细胞RNA测序。一种用于提高造血研究中灵敏度和可重复性的简化工作流程。人脐带血来源的造血干细胞和祖细胞的应用。
Front Cell Dev Biol. 2025 May 15;13:1590889. doi: 10.3389/fcell.2025.1590889. eCollection 2025.
6
Mutant CEBPA promotes tolerance to inflammatory stress through deficient AP-1 activation.突变型CEBPA通过AP-1激活缺陷促进对炎症应激的耐受性。
Nat Commun. 2025 Apr 12;16(1):3492. doi: 10.1038/s41467-025-58712-7.
7
TFcomb identifies transcription factor combinations for cellular reprogramming based on single-cell multiomics data.TFcomb基于单细胞多组学数据识别用于细胞重编程的转录因子组合。
Genome Res. 2025 Jun 2;35(6):1429-1439. doi: 10.1101/gr.279955.124.
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Two- and Three-Dimensional In Vitro Models of Parkinson's and Alzheimer's Diseases: State-of-the-Art and Applications.帕金森病和阿尔茨海默病的二维和三维体外模型:现状与应用
Int J Mol Sci. 2025 Jan 13;26(2):620. doi: 10.3390/ijms26020620.
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Front Cell Dev Biol. 2025 Jan 3;12:1463807. doi: 10.3389/fcell.2024.1463807. eCollection 2024.
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造血细胞因子可指导谱系选择。
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4
Cells keep a memory of their tissue origin during axolotl limb regeneration.在蝾螈肢体再生过程中,细胞保留着它们组织起源的记忆。
Nature. 2009 Jul 2;460(7251):60-5. doi: 10.1038/nature08152.
5
Elite and stochastic models for induced pluripotent stem cell generation.诱导多能干细胞生成的精英模型和随机模型。
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