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探索体内重编程在研究胚胎发育、组织再生和机体衰老方面的潜力。

Exploring the potential of in vivo reprogramming for studying embryonic development, tissue regeneration, and organismal aging.

机构信息

Department of Molecular Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo 113-0033, Japan.

出版信息

Curr Opin Genet Dev. 2023 Aug;81:102067. doi: 10.1016/j.gde.2023.102067. Epub 2023 Jun 23.

DOI:10.1016/j.gde.2023.102067
PMID:37356342
Abstract

Forced expression of a specific set of transcription factors can reprogram terminally differentiated cells and convert them into induced pluripotent stem cells that correspond to cells in the inner cell mass of the developing embryo. It is now recognized that the scope of the reprogramming factors extends far beyond the stem cell biology. Studies using mouse models demonstrated that the induction of the reprogramming factors promotes cellular reprogramming in vivo. Closer inspection of these mice has revealed that expression of the reprogramming factors results in unique consequences that are not seen when cells are reprogrammed ex vivo, and can provide insights into development, tissue regeneration, cancer, and aging.

摘要

特定转录因子的强制表达可以重编程终末分化细胞,并将其转化为诱导多能干细胞,这些细胞与发育胚胎的内细胞团中的细胞相对应。现在人们已经认识到,重编程因子的范围远远超出了干细胞生物学。使用小鼠模型的研究表明,重编程因子的诱导促进了体内细胞的重编程。对这些小鼠的更仔细检查表明,重编程因子的表达导致了独特的后果,而这些后果在体外细胞重编程时是不会出现的,并且可以为发育、组织再生、癌症和衰老提供新的见解。

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Exploring the potential of in vivo reprogramming for studying embryonic development, tissue regeneration, and organismal aging.探索体内重编程在研究胚胎发育、组织再生和机体衰老方面的潜力。
Curr Opin Genet Dev. 2023 Aug;81:102067. doi: 10.1016/j.gde.2023.102067. Epub 2023 Jun 23.
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Unveiling epigenetic regulation in cancer, aging, and rejuvenation with in vivo reprogramming technology.利用体内重编程技术揭示癌症、衰老和 rejuvenation 中的表观遗传调控。
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Reprogramming of 3' untranslated regions of mRNAs by alternative polyadenylation in generation of pluripotent stem cells from different cell types.多能干细胞的产生中通过可变多聚腺苷酸化重编程 mRNAs 的 3' 非翻译区。
PLoS One. 2009 Dec 23;4(12):e8419. doi: 10.1371/journal.pone.0008419.
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Robust Differentiation of mRNA-Reprogrammed Human Induced Pluripotent Stem Cells Toward a Retinal Lineage.mRNA重编程的人类诱导多能干细胞向视网膜谱系的稳健分化
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High throughput sequencing identifies an imprinted gene, Grb10, associated with the pluripotency state in nuclear transfer embryonic stem cells.高通量测序鉴定出一个与核移植胚胎干细胞多能性状态相关的印记基因Grb10。
Oncotarget. 2017 Jul 18;8(29):47344-47355. doi: 10.18632/oncotarget.17185.
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Genome-wide gene expression analyses reveal unique cellular characteristics related to the amenability of HPC/HSCs into high-quality induced pluripotent stem cells.全基因组基因表达分析揭示了与造血祖细胞/造血干细胞向高质量诱导多能干细胞转化的易感性相关的独特细胞特征。
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In vivo reprogramming for tissue regeneration and organismal rejuvenation.体内重编程用于组织再生和机体 rejuvenation。
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Concise review: Induced pluripotent stem cells versus embryonic stem cells: close enough or yet too far apart?简明综述:诱导多能干细胞与胚胎干细胞:足够接近还是相差甚远?
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Divergent reprogramming routes lead to alternative stem-cell states.不同的重编程途径导致不同的干细胞状态。
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Induced pluripotent reprogramming from promiscuous human stemness related factors.诱导多能重编程从杂乱无章的人类干性相关因子。
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