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体内重编程作为心脏再生治疗的一种新方法。

In vivo reprogramming as a new approach to cardiac regenerative therapy.

机构信息

Department of Cardiology, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba City, Ibaraki 305-8575, Japan.

Department of Cardiology, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba City, Ibaraki 305-8575, Japan.

出版信息

Semin Cell Dev Biol. 2022 Feb;122:21-27. doi: 10.1016/j.semcdb.2021.06.019. Epub 2021 Jun 29.

Abstract

Cardiovascular diseases are a common cause of death worldwide. Adult cardiomyocytes have limited regenerative capacity after injury, and there is growing interest in cardiac regeneration as a new therapeutic strategy. There are several limitations of induced pluripotent stem cell-based transplantation therapy with respect to efficiency and risks of tumorigenesis. Direct reprogramming enables the conversion of terminally differentiated cells into target cell types using defined factors. In most cardiac diseases, activated fibroblasts proliferate in the damaged heart and contribute to the progression of heart failure. In vivo cardiac reprogramming, in which resident cardiac fibroblasts are converted into cardiomyocytes in situ, is expected to become a new cardiac regenerative therapy. Indeed, we and other groups have demonstrated that in vivo reprogramming improves cardiac function and reduces fibrosis after myocardial infarction. In this review, we summarize recent discoveries and developments related to in vivo reprogramming. In addition, issues that need to be resolved for clinical application are described.

摘要

心血管疾病是全球范围内常见的死亡原因。成体心肌细胞在损伤后再生能力有限,因此人们越来越关注心脏再生作为一种新的治疗策略。基于诱导多能干细胞的移植治疗在效率和致瘤风险方面存在一些局限性。直接重编程可利用定义好的因子将终末分化细胞转化为目标细胞类型。在大多数心脏疾病中,激活的成纤维细胞在受损心脏中增殖,并促进心力衰竭的进展。体内心脏重编程,即将驻留的心肌成纤维细胞原位转化为心肌细胞,有望成为一种新的心脏再生治疗方法。事实上,我们和其他研究小组已经证明,体内重编程可改善心肌梗死后的心脏功能并减少纤维化。在这篇综述中,我们总结了与体内重编程相关的最新发现和进展。此外,还描述了临床应用中需要解决的问题。

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