Department of Biomedical Engineering, Columbia University, 622 West 168th Street, VC12-234, New York, New York 10032, United States.
Department of Medicine, Columbia University, 622 West 168th Street, VC12-234, New York, New York 10032, United States.
ACS Biomater Sci Eng. 2021 Nov 8;7(11):5215-5229. doi: 10.1021/acsbiomaterials.1c01006. Epub 2021 Oct 20.
Engineered cardiac tissues derived from human induced pluripotent stem cells (iPSCs) are increasingly used for drug discovery, pharmacology and in models of development and disease. While there are numerous platforms to engineer cardiac tissues, they often require expensive and nonconventional equipment and utilize complex video-processing algorithms. As a result, only specialized academic laboratories have been able to harness this technology. In addition, methodologies and tissue features have been challenging to reproduce between different groups and models. Here, we describe a facile technology (milliPillar) that covers the entire pipeline required for studies of engineered cardiac tissues. We include methodologies for (i) platform fabrication, (ii) cardiac tissue generation, (iii) electrical stimulation, (iv) automated real-time data acquisition, and (v) advanced video analyses. We validate these methodologies and demonstrate the versatility of the platform by showcasing the fabrication of tissues in different hydrogel materials and using cardiomyocytes derived from different iPSC lines in combination with different types of stromal cells. We also validate the long-term culture of tissues within the platform and provide protocols for automated analysis of force generation and calcium flux using both brightfield and fluorescence imaging. Lastly, we demonstrate the compatibility of the milliPillar platform with electromechanical stimulation to enhance cardiac tissue function. We expect that this resource will provide a valuable and user-friendly tool for the generation and real-time assessment of engineered human cardiac tissues for basic and translational studies.
由人诱导多能干细胞(iPSC)衍生的工程化心脏组织越来越多地用于药物发现、药理学以及发育和疾病模型中。虽然有许多用于构建心脏组织的平台,但它们通常需要昂贵且非常规的设备,并使用复杂的视频处理算法。因此,只有专门的学术实验室才能够利用这项技术。此外,不同组和模型之间的方法和组织特征难以重现。在这里,我们描述了一种简便的技术(毫柱),该技术涵盖了用于工程化心脏组织研究的整个流程。我们包括用于(i)平台制造、(ii)心脏组织生成、(iii)电刺激、(iv)自动实时数据采集和(v)高级视频分析的方法。我们验证了这些方法,并通过展示在不同水凝胶材料中制造组织以及将源自不同 iPSC 系的心肌细胞与不同类型的基质细胞结合使用来展示平台的多功能性。我们还验证了平台内组织的长期培养,并提供了使用明场和荧光成像进行力生成和钙通量自动分析的方案。最后,我们证明了毫柱平台与机电刺激的兼容性,以增强心脏组织功能。我们希望这个资源将为基础和转化研究中生成和实时评估工程化人类心脏组织提供一个有价值且易于使用的工具。