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人类心脏疾病的三维微工程模型

Three-dimensional microengineered models of human cardiac diseases.

作者信息

Veldhuizen Jaimeson, Migrino Raymond Q, Nikkhah Mehdi

机构信息

1School of Biological and Health Systems Engineering (SBHSE), Arizona State University, 501 E Tyler Mall Building ECG, Suite 334, Tempe, AZ 85287-9709 USA.

Phoenix Veterans Affairs Health Care System, Phoenix, AZ 85012 USA.

出版信息

J Biol Eng. 2019 Apr 3;13:29. doi: 10.1186/s13036-019-0155-6. eCollection 2019.

DOI:10.1186/s13036-019-0155-6
PMID:30988697
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6448321/
Abstract

In vitro three-dimensional (3D) microengineered tissue models have been the recent focus of pathophysiological studies, particularly in the field of cardiovascular research. These models, as classified by 3D biomimetic tissues within micrometer-scale platforms, enable precise environmental control on the molecular- and cellular-levels to elucidate biological mechanisms of disease progression and enhance efficacy of therapeutic research. Microengineered models also incorporate directed stem cell differentiation and genome modification techniques that warrant derivation of patient-specific and genetically-edited human cardiac cells for precise recapitulation of diseased tissues. Additionally, integration of added functionalities and/or structures into these models serves to enhance the capability to further extract disease-specific phenotypic, genotypic, and electrophysiological information. This review highlights the recent progress in the development of in vitro 3D microengineered models for study of cardiac-related diseases (denoted as CDs). We will primarily provide a brief overview on currently available 2D assays and animal models for studying of CDs. We will further expand our discussion towards currently available 3D microengineered cardiac tissue models and their implementation for study of specific disease conditions.

摘要

体外三维(3D)微工程组织模型已成为近期病理生理学研究的焦点,尤其是在心血管研究领域。这些模型,按照微米级平台内的3D仿生组织分类,能够在分子和细胞水平上进行精确的环境控制,以阐明疾病进展的生物学机制,并提高治疗研究的效果。微工程模型还纳入了定向干细胞分化和基因组编辑技术,这保证了能够衍生出患者特异性和基因编辑的人类心脏细胞,以精确再现患病组织。此外,将附加功能和/或结构整合到这些模型中,有助于增强进一步提取疾病特异性表型、基因型和电生理信息的能力。本综述重点介绍了用于研究心脏相关疾病(简称为CDs)的体外3D微工程模型开发的最新进展。我们将主要简要概述目前用于研究CDs的二维检测方法和动物模型。我们还将进一步扩展讨论,涉及目前可用的3D微工程心脏组织模型及其在特定疾病状况研究中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fa/6448321/285a410d9769/13036_2019_155_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fa/6448321/909258cbd006/13036_2019_155_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fa/6448321/a1d835719dfc/13036_2019_155_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fa/6448321/285a410d9769/13036_2019_155_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fa/6448321/909258cbd006/13036_2019_155_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fa/6448321/a1d835719dfc/13036_2019_155_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fa/6448321/285a410d9769/13036_2019_155_Fig3_HTML.jpg

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