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简明综述:多能干细胞来源的人心脏心肌细胞特定腔室分类标准

Concise Review: Criteria for Chamber-Specific Categorization of Human Cardiac Myocytes Derived from Pluripotent Stem Cells.

作者信息

Kane Christopher, Terracciano Cesare M N

机构信息

Imperial College London, National Heart and Lung Institute, Hammersmith Campus, BHF Centre for Regenerative Medicine, London, United Kingdom.

出版信息

Stem Cells. 2017 Aug;35(8):1881-1897. doi: 10.1002/stem.2649. Epub 2017 Jun 27.

DOI:10.1002/stem.2649
PMID:28577296
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5575566/
Abstract

Human pluripotent stem cell-derived cardiomyocytes (PSC-CMs) have great potential application in almost all areas of cardiovascular research. A current major goal of the field is to build on the past success of differentiation strategies to produce CMs with the properties of those originating from the different chambers of the adult human heart. With no anatomical origin or developmental pathway to draw on, the question of how to judge the success of such approaches and assess the chamber specificity of PSC-CMs has become increasingly important; commonly used methods have substantial limitations and are based on limited evidence to form such an assessment. In this article, we discuss the need for chamber-specific PSC-CMs in a number of areas as well as current approaches used to assess these cells on their likeness to those from different chambers of the heart. Furthermore, describing in detail the structural and functional features that distinguish the different chamber-specific human adult cardiac myocytes, we propose an evidence-based tool to aid investigators in the phenotypic characterization of differentiated PSC-CMs. Stem Cells 2017;35:1881-1897.

摘要

人多能干细胞衍生的心肌细胞(PSC-CMs)在心血管研究的几乎所有领域都具有巨大的潜在应用价值。该领域当前的一个主要目标是在过去分化策略成功的基础上,培育出具有源自成年人心脏不同腔室心肌细胞特性的心肌细胞。由于没有解剖学起源或发育途径可供借鉴,如何判断此类方法的成功以及评估PSC-CMs的腔室特异性问题变得越来越重要;常用方法存在重大局限性,且基于有限证据来形成此类评估。在本文中,我们讨论了在多个领域中对腔室特异性PSC-CMs的需求,以及用于评估这些细胞与来自心脏不同腔室细胞相似性的当前方法。此外,我们详细描述了区分不同腔室特异性成人心脏心肌细胞的结构和功能特征,提出了一种基于证据的工具,以帮助研究人员对分化的PSC-CMs进行表型特征分析。《干细胞》2017年;35:1881 - 1897。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de56/5575566/cdf090d03c17/STEM-35-1881-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de56/5575566/126310c5359f/STEM-35-1881-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de56/5575566/8e5572384611/STEM-35-1881-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de56/5575566/885e5f75bc1f/STEM-35-1881-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de56/5575566/33e6b9d42ce8/STEM-35-1881-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de56/5575566/cdf090d03c17/STEM-35-1881-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de56/5575566/126310c5359f/STEM-35-1881-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de56/5575566/8e5572384611/STEM-35-1881-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de56/5575566/885e5f75bc1f/STEM-35-1881-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de56/5575566/33e6b9d42ce8/STEM-35-1881-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de56/5575566/cdf090d03c17/STEM-35-1881-g005.jpg

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