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3D cardiac μtissues within a microfluidic device with real-time contractile stress readout.微流控装置内具有实时收缩应力读数的3D心脏微组织。
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Engineered heart tissues and induced pluripotent stem cells: Macro- and microstructures for disease modeling, drug screening, and translational studies.工程化心脏组织与诱导多能干细胞:用于疾病建模、药物筛选及转化研究的宏观与微观结构
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Human engineered heart tissue as a model system for drug testing.人工程心脏组织作为药物测试的模型系统。
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Mechanical Stress Promotes Maturation of Human Myocardium From Pluripotent Stem Cell-Derived Progenitors.机械应力促进多能干细胞衍生祖细胞来源的人心肌成熟。
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Human iPSC-based cardiac microphysiological system for drug screening applications.用于药物筛选应用的基于人诱导多能干细胞的心脏微生理系统。
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Mechanism of automaticity in cardiomyocytes derived from human induced pluripotent stem cells.人诱导多能干细胞来源的心肌细胞的自律性机制。
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Image-based evaluation of contraction-relaxation kinetics of human-induced pluripotent stem cell-derived cardiomyocytes: Correlation and complementarity with extracellular electrophysiology.基于图像的人诱导多能干细胞衍生心肌细胞收缩-松弛动力学评估:与细胞外电生理学的相关性和互补性。
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Generation of strip-format fibrin-based engineered heart tissue (EHT).带状纤维蛋白基工程心脏组织(EHT)的生成。
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利用磁传感对诱导多能干细胞来源的工程化人心脏组织进行实时力和频率分析。

Real-Time Force and Frequency Analysis of Engineered Human Heart Tissue Derived from Induced Pluripotent Stem Cells Using Magnetic Sensing.

作者信息

Bielawski Kevin S, Leonard Andrea, Bhandari Shiv, Murry Chuck E, Sniadecki Nathan J

机构信息

1 Department of Mechanical Engineering, University of Washington , Seattle, Washington.

2 Center for Cardiovascular Biology, University of Washington , Seattle, Washington.

出版信息

Tissue Eng Part C Methods. 2016 Oct;22(10):932-940. doi: 10.1089/ten.TEC.2016.0257. Epub 2016 Sep 28.

DOI:10.1089/ten.TEC.2016.0257
PMID:27600722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5079417/
Abstract

Engineered heart tissues made from human pluripotent stem cell-derived cardiomyocytes have been used for modeling cardiac pathologies, screening new therapeutics, and providing replacement cardiac tissue. Current methods measure the functional performance of engineered heart tissue by their twitch force and beating frequency, typically obtained by optical measurements. In this article, we describe a novel method for assessing twitch force and beating frequency of engineered heart tissue using magnetic field sensing, which enables multiple tissues to be measured simultaneously. The tissues are formed as thin structures suspended between two silicone posts, where one post is rigid and another is flexible and contains an embedded magnet. When the tissue contracts it causes the flexible post to bend in proportion to its twitch force. We measured the bending of the post using giant magnetoresistive (GMR) sensors located underneath a 24-well plate containing the tissues. We validated the accuracy of the readings from the GMR sensors against optical measurements. We demonstrated the utility and sensitivity of our approach by testing the effects of three concentrations of isoproterenol and verapamil on twitch force and beating frequency in real-time, parallel experiments. This system should be scalable beyond the 24-well format, enabling greater automation in assessing the contractile function of cardiomyocytes in a tissue-engineered environment.

摘要

由人类多能干细胞衍生的心肌细胞制成的工程心脏组织已被用于模拟心脏病理、筛选新疗法以及提供替代心脏组织。目前的方法通过工程心脏组织的抽搐力和跳动频率来衡量其功能性能,这些通常通过光学测量获得。在本文中,我们描述了一种使用磁场传感评估工程心脏组织抽搐力和跳动频率的新方法,该方法能够同时测量多个组织。组织形成为悬浮在两个硅胶柱之间的薄结构,其中一个柱是刚性的,另一个是柔性的且包含一个嵌入式磁体。当组织收缩时,它会使柔性柱根据其抽搐力成比例弯曲。我们使用位于装有组织的24孔板下方的巨磁阻(GMR)传感器测量柱的弯曲。我们对照光学测量验证了GMR传感器读数的准确性。我们通过在实时平行实验中测试三种浓度的异丙肾上腺素和维拉帕米对抽搐力和跳动频率的影响,证明了我们方法的实用性和灵敏度。该系统应该能够扩展到24孔板格式之外,在组织工程环境中评估心肌细胞收缩功能时实现更大的自动化。