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本文引用的文献

1
MicroRNA therapy stimulates uncontrolled cardiac repair after myocardial infarction in pigs.microRNA 疗法刺激猪心肌梗死后不受控制的心脏修复。
Nature. 2019 May;569(7756):418-422. doi: 10.1038/s41586-019-1191-6. Epub 2019 May 8.
2
Transient Introduction of miR-294 in the Heart Promotes Cardiomyocyte Cell Cycle Reentry After Injury.短暂引入 miR-294 可促进损伤后心肌细胞周期再进入。
Circ Res. 2019 Jun 21;125(1):14-25. doi: 10.1161/CIRCRESAHA.118.314223. Epub 2019 Apr 9.
3
The Role of Thyroid Hormones in Heart Failure.甲状腺激素在心力衰竭中的作用。
Cardiovasc Drugs Ther. 2019 Apr;33(2):179-188. doi: 10.1007/s10557-019-06870-4.
4
Evidence for hormonal control of heart regenerative capacity during endothermy acquisition.证据表明,在恒温动物获得过程中,激素控制着心脏再生能力。
Science. 2019 Apr 12;364(6436):184-188. doi: 10.1126/science.aar2038. Epub 2019 Mar 7.
5
Immune cells as targets for cardioprotection: new players and novel therapeutic opportunities.免疫细胞作为心脏保护的靶点:新的参与者和新的治疗机会。
Cardiovasc Res. 2019 Jun 1;115(7):1117-1130. doi: 10.1093/cvr/cvz050.
6
Heart Disease and Stroke Statistics-2019 Update: A Report From the American Heart Association.《2019年心脏病和中风统计数据更新:美国心脏协会报告》
Circulation. 2019 Mar 5;139(10):e56-e528. doi: 10.1161/CIR.0000000000000659.
7
Hippo Deficiency Leads to Cardiac Dysfunction Accompanied by Cardiomyocyte Dedifferentiation During Pressure Overload.Hippo 信号缺失导致压力超负荷时心肌细胞去分化伴随的心脏功能障碍。
Circ Res. 2019 Jan 18;124(2):292-305. doi: 10.1161/CIRCRESAHA.118.314048.
8
IL-13 promotes in vivo neonatal cardiomyocyte cell cycle activity and heart regeneration.IL-13 促进体内新生大鼠心肌细胞的细胞周期活性和心脏再生。
Am J Physiol Heart Circ Physiol. 2019 Jan 1;316(1):H24-H34. doi: 10.1152/ajpheart.00521.2018. Epub 2018 Oct 19.
9
A conserved HH-Gli1-Mycn network regulates heart regeneration from newt to human.保守的 HH-Gli1-Mycn 网络调控蝾螈到人类的心脏再生。
Nat Commun. 2018 Oct 12;9(1):4237. doi: 10.1038/s41467-018-06617-z.
10
Concise Review: Heart-Derived Cell Therapy 2.0: Paracrine Strategies to Increase Therapeutic Repair of Injured Myocardium.简明综述:心脏源细胞治疗 2.0:旁分泌策略增加受损心肌的治疗修复。
Stem Cells. 2018 Dec;36(12):1794-1803. doi: 10.1002/stem.2910. Epub 2018 Oct 15.

心脏再生的分子机制。

Molecular mechanisms of heart regeneration.

机构信息

Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, 02138, USA.

Department of Stem Cell and Regenerative Biology and the Harvard Stem Cell Institute, Harvard University, Cambridge, MA, 02138, USA; Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 02115, USA.

出版信息

Semin Cell Dev Biol. 2020 Apr;100:20-28. doi: 10.1016/j.semcdb.2019.09.003. Epub 2019 Oct 4.

DOI:10.1016/j.semcdb.2019.09.003
PMID:31587963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7071978/
Abstract

The adult mammalian heart is incapable of clinically relevant regeneration. The regenerative deficit in adult mammalian heart contrasts with the fetal and neonatal heart, which demonstrate substantial regenerative capacity after injury. This deficiency in adult mammals is attributable to the lack of resident stem cells after birth, combined with an inability of pre-existing cardiomyocytes to complete cytokinesis. Studies of neonatal heart regeneration in mammals suggest that latent regenerative potential can be re-activated. Dissecting the cellular and molecular mechanisms that promote cardiomyocyte proliferation is key to stimulating true regeneration in adult humans. Here, we review recent advances in our understanding of cardiomyocyte proliferation that suggest molecular approaches to heart regeneration.

摘要

成年哺乳动物的心脏无法进行临床上有意义的再生。成年哺乳动物的心脏在再生方面存在缺陷,而胎儿和新生儿的心脏在受到损伤后具有很强的再生能力。哺乳动物成年后缺乏驻留干细胞,加上原有心肌细胞无法完成胞质分裂,这是造成成年哺乳动物心脏再生能力缺陷的原因。对哺乳动物新生儿心脏再生的研究表明,潜在的再生能力可以被重新激活。解析促进心肌细胞增殖的细胞和分子机制是刺激成年人类真正再生的关键。在这里,我们回顾了最近在理解心肌细胞增殖方面的进展,这些进展为心脏再生提供了分子方法。