通过直接重编程实现心脏再生。

IF 5 3区 医学 Q2 IMMUNOLOGY
Hiroyuki Yamakawa, Masaki Ieda
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引用次数: 15

摘要

由于生活方式西化和人口老龄化,日本的心脏病发病率不断上升。在传统干预不合适的情况下,再生医学提供了一个有希望的治疗选择。然而,干细胞的使用有局限性,因此,“直接心脏重编程”正在成为一种替代治疗方法。心肌再生将心肌成纤维细胞原位转分化为心肌细胞。三种心源性转录因子:Gata4, Mef2c和Tbx5 (GMT)可以在小鼠中诱导成纤维细胞直接重编程为诱导心肌细胞(iCMs)。然而,在人类中,需要额外的因子,如Mesp1和心肌。炎症和免疫反应阻碍了小鼠的重编程过程,而TET1等表观遗传修饰因子参与了人类心脏的直接重编程。提高重编程效率的三个主要途径是:(1)改善直接心脏重编程因子,(2)改善细胞培养条件,(3)调节表观遗传因子。miR-133是第一种方法的潜在候选者。对于第二种方法,TGF-β和Wnt信号抑制剂、Akt1过表达、Notch信号通路抑制剂,如DAPT ((S)-叔丁基2-((S)-2-(2-(3,5-二氟苯基)乙酰氨基)丙胺)-2-苯乙酸)、成纤维细胞生长因子(FGF)-2、FGF-10和血管内皮生长因子(VEGF: FFV)可以影响重编程。第三种方法是降低Bmi1的表达,Bmi1调节组蛋白H2A的单泛素化,改变组蛋白修饰,进而改变重编程效率。此外,非甾体抗炎药双氯芬酸和Mef2c高水平过表达可改善心脏直接重编程。如果要将直接心脏重编程用于人类,则需要改进,而且涉及的分子机制在很大程度上仍然难以捉摸。心脏重编程研究的进一步进展需要使我们更接近心脏再生治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cardiac regeneration by direct reprogramming in this decade and beyond.

Cardiac regeneration by direct reprogramming in this decade and beyond.

Cardiac regeneration by direct reprogramming in this decade and beyond.

Cardiac regeneration by direct reprogramming in this decade and beyond.

Japan faces an increasing incidence of heart disease, owing to a shift towards a westernized lifestyle and an aging demographic. In cases where conventional interventions are not appropriate, regenerative medicine offers a promising therapeutic option. However, the use of stem cells has limitations, and therefore, "direct cardiac reprogramming" is emerging as an alternative treatment. Myocardial regeneration transdifferentiates cardiac fibroblasts into cardiomyocytes in situ.Three cardiogenic transcription factors: Gata4, Mef2c, and Tbx5 (GMT) can induce direct reprogramming of fibroblasts into induced cardiomyocytes (iCMs), in mice. However, in humans, additional factors, such as Mesp1 and Myocd, are required. Inflammation and immune responses hinder the reprogramming process in mice, and epigenetic modifiers such as TET1 are involved in direct cardiac reprogramming in humans. The three main approaches to improving reprogramming efficiency are (1) improving direct cardiac reprogramming factors, (2) improving cell culture conditions, and (3) regulating epigenetic factors. miR-133 is a potential candidate for the first approach. For the second approach, inhibitors of TGF-β and Wnt signals, Akt1 overexpression, Notch signaling pathway inhibitors, such as DAPT ((S)-tert-butyl 2-((S)-2-(2-(3,5-difluorophenyl) acetamido) propanamido)-2-phenylacetate), fibroblast growth factor (FGF)-2, FGF-10, and vascular endothelial growth factor (VEGF: FFV) can influence reprogramming. Reducing the expression of Bmi1, which regulates the mono-ubiquitination of histone H2A, alters histone modification, and subsequently the reprogramming efficiency, in the third approach. In addition, diclofenac, a non-steroidal anti-inflammatory drug, and high level of Mef2c overexpression could improve direct cardiac reprogramming.Direct cardiac reprogramming needs improvement if it is to be used in humans, and the molecular mechanisms involved remain largely elusive. Further advances in cardiac reprogramming research are needed to bring us closer to cardiac regenerative therapy.

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来源期刊
CiteScore
11.10
自引率
1.20%
发文量
45
审稿时长
11 weeks
期刊介绍: Inflammation and Regeneration is the official journal of the Japanese Society of Inflammation and Regeneration (JSIR). This journal provides an open access forum which covers a wide range of scientific topics in the basic and clinical researches on inflammation and regenerative medicine. It also covers investigations of infectious diseases, including COVID-19 and other emerging infectious diseases, which involve the inflammatory responses. Inflammation and Regeneration publishes papers in the following categories: research article, note, rapid communication, case report, review and clinical drug evaluation.
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