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直接心脏重编程——将心脏成纤维细胞转化为心肌细胞。

Direct Cardiac Reprogramming - Converting Cardiac Fibroblasts to Cardiomyocytes.

作者信息

Sadahiro Taketaro

机构信息

Department of Cardiology, Faculty of Medicine, University of Tsukuba Tsukuba Japan.

出版信息

Circ Rep. 2019 Nov 12;1(12):564-567. doi: 10.1253/circrep.CR-19-0104.

DOI:10.1253/circrep.CR-19-0104
PMID:33693102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7897695/
Abstract

Cardiovascular disease is the leading cause of death and disability worldwide. Despite advances in cardiovascular therapy, mortality in heart disease still remains high. Direct cardiac reprogramming is a promising approach for cardiac tissue repair involving in situ generation of new cardiomyocytes from endogenous cardiac fibroblasts. Although, initially, the reprogramming efficiency was low, several developments in reprogramming methods have improved the in vitro cardiac reprogramming efficiency. Subsequently, in vivo cardiac reprogramming has demonstrated improvement in cardiac function and fibrosis after myocardial infarction. Here, we review recent progress in cardiac reprogramming as a new technology for cardiac regeneration.

摘要

心血管疾病是全球范围内导致死亡和残疾的主要原因。尽管心血管治疗取得了进展,但心脏病的死亡率仍然很高。直接心脏重编程是一种有前景的心脏组织修复方法,涉及从内源性心脏成纤维细胞原位生成新的心肌细胞。虽然最初重编程效率较低,但重编程方法的一些进展提高了体外心脏重编程效率。随后,体内心脏重编程已证明在心肌梗死后心脏功能和纤维化方面有所改善。在此,我们综述心脏重编程作为心脏再生新技术的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b96/7897695/beb1593e7532/circrep-1-564-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b96/7897695/beb1593e7532/circrep-1-564-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b96/7897695/beb1593e7532/circrep-1-564-g001.jpg

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本文引用的文献

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Context-Specific Transcription Factor Functions Regulate Epigenomic and Transcriptional Dynamics during Cardiac Reprogramming.语境特异性转录因子功能调控心脏重编程过程中的表观遗传和转录动力学。
Cell Stem Cell. 2019 Jul 3;25(1):87-102.e9. doi: 10.1016/j.stem.2019.06.012.
2
Single-Cell Transcriptomic Analyses of Cell Fate Transitions during Human Cardiac Reprogramming.单细胞转录组分析人类心脏重编程过程中的细胞命运转变。
Cell Stem Cell. 2019 Jul 3;25(1):149-164.e9. doi: 10.1016/j.stem.2019.05.020. Epub 2019 Jun 20.
3
Cardiac Reprogramming Factors Synergistically Activate Genome-wide Cardiogenic Stage-Specific Enhancers.
心脏重编程因子协同激活全基因组心脏发生阶段特异性增强子。
Cell Stem Cell. 2019 Jul 3;25(1):69-86.e5. doi: 10.1016/j.stem.2019.03.022. Epub 2019 May 9.
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Role of cyclooxygenase-2-mediated prostaglandin E2-prostaglandin E receptor 4 signaling in cardiac reprogramming.环氧化酶-2 介导的前列腺素 E2-前列腺素 E 受体 4 信号在心脏重编程中的作用。
Nat Commun. 2019 Feb 20;10(1):674. doi: 10.1038/s41467-019-08626-y.
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Specialized fibroblast differentiated states underlie scar formation in the infarcted mouse heart.特化的成纤维细胞分化状态是导致梗死小鼠心脏形成瘢痕的基础。
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Direct In Vivo Reprogramming with Sendai Virus Vectors Improves Cardiac Function after Myocardial Infarction.仙台病毒载体的直接体内重编程可改善心肌梗死后的心脏功能。
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Induced Pluripotent Stem Cells 10 Years Later: For Cardiac Applications.诱导多能干细胞 10 年后:心脏应用。
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Chemical Enhancement of In Vitro and In Vivo Direct Cardiac Reprogramming.体外和体内直接心脏重编程的化学增强作用
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