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通过细胞重编程再生心血管系统:当前方法与未来展望

Regenerating the Cardiovascular System Through Cell Reprogramming; Current Approaches and a Look Into the Future.

作者信息

Tsifaki Marianna, Kelaini Sophia, Caines Rachel, Yang Chunbo, Margariti Andriana

机构信息

The Wellcome-Wolfson Building, Centre for Experimental Medicine, Queen's University Belfast, Belfast, United Kingdom.

出版信息

Front Cardiovasc Med. 2018 Aug 20;5:109. doi: 10.3389/fcvm.2018.00109. eCollection 2018.

Abstract

Cardiovascular disease (CVD), despite the advances of the medical field, remains one of the leading causes of mortality worldwide. Discovering novel treatments based on cell therapy or drugs is critical, and induced pluripotent stem cells (iPS Cells) technology has made it possible to design extensive disease-specific models. Elucidating the differentiation process challenged our previous knowledge of cell plasticity and capabilities and allows the concept of cell reprogramming technology to be established, which has inspired the creation of both and techniques. Patient-specific cell lines provide the opportunity of studying their pathophysiology , which can lead to novel drug development. At the same time, models have been designed where transdifferentiation of cell populations into cardiomyocytes or endothelial cells (ECs) give hope toward effective cell therapies. Unfortunately, the efficiency as well as the concerns about the safety of all these methods make it exceedingly difficult to pass to the clinical trial phase. It is our opinion that creating an model out of patient-specific cells will be one of the most important goals in the future to help surpass all these hindrances. Thus, in this review we aim to present the current state of research in reprogramming toward the cardiovascular system's regeneration, and showcase how the development and study of a multicellular 3D model will improve our fighting chances.

摘要

尽管医学领域不断进步,但心血管疾病(CVD)仍是全球主要死因之一。基于细胞疗法或药物发现新的治疗方法至关重要,而诱导多能干细胞(iPS细胞)技术使设计广泛的疾病特异性模型成为可能。阐明分化过程挑战了我们以前对细胞可塑性和能力的认识,并使细胞重编程技术的概念得以确立,这激发了细胞重编程和转分化技术的创造。患者特异性细胞系提供了研究其病理生理学的机会,这可能会带来新的药物开发。同时,已经设计出模型,其中细胞群体向心肌细胞或内皮细胞(ECs)的转分化为有效的细胞疗法带来了希望。不幸的是,所有这些方法的效率以及对安全性的担忧使得进入临床试验阶段极其困难。我们认为,利用患者特异性细胞创建一个体外模型将是未来帮助克服所有这些障碍的最重要目标之一。因此,在本综述中,我们旨在介绍心血管系统再生重编程的当前研究状态,并展示多细胞3D体外模型的开发和研究将如何提高我们成功的几率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aff/6109758/0fc00e76833f/fcvm-05-00109-g0001.jpg

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