直接心脏重编程用于心血管再生和分化。

IF 1.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL KEIO JOURNAL OF MEDICINE Pub Date : 2020-09-25 Epub Date: 2020-01-09 DOI:10.2302/kjm.2019-0008-OA
Taketaro Sadahiro, Masaki Ieda
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引用次数: 4

摘要

心血管疾病是世界范围内导致死亡的主要原因。心肌细胞的再生能力有限;因此,对再生疗法的需求很大。目前有几种潜在的心脏再生策略,其中一种方法涉及从内源性细胞来源原位生成新的心肌细胞。直接心脏重编程已经成为一种新的治疗方法,通过直接将内源性心脏成纤维细胞转化为心肌细胞样细胞来再生受损的心脏。在我们的第一份直接心脏重编程报告之后,重大进展已经阐明了与心脏重编程相关的分子机制。这些进步也通过直接在体内进行心脏重编程提高了心脏重编程效率。此外,人类成纤维细胞的心脏重编程也取得了进展。尽管基础研究支持了该领域的实质性进展,但在临床应用方面仍存在许多挑战。在这里,我们回顾了心脏重编程作为一种理解和治疗心血管疾病的新技术的现状。
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Direct Cardiac Reprogramming for Cardiovascular Regeneration and Differentiation.

Cardiovascular disease is the leading cause of death worldwide. Cardiomyocytes have limited regenerative capacity; consequently, regenerative therapies are in high demand. There are currently several potential strategies for heart regeneration, with one approach involving in situ generation of new cardiomyocytes from endogenous cell sources. Direct cardiac reprogramming has emerged as a novel therapeutic approach to regenerating the damaged heart by directly converting endogenous cardiac fibroblasts into cardiomyocyte-like cells. Following our first report of direct cardiac reprogramming, significant advances have elucidated the molecular mechanisms associated with cardiac reprogramming. These advances have also improved cardiac-reprogramming efficiency by enabling direct in vivo cardiac reprogramming. Moreover, progress has been made in cardiac reprogramming of human fibroblasts. Although basic research has supported substantial progress in this field, numerous challenges remain in terms of clinical application. Here, we review the current state of cardiac reprogramming as a new technology for understanding and treating cardiovascular diseases.

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来源期刊
KEIO JOURNAL OF MEDICINE
KEIO JOURNAL OF MEDICINE MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.10
自引率
0.00%
发文量
23
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