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用于研究人类心脏组织生理学的多参数切片培养平台。

Multiparametric slice culture platform for the investigation of human cardiac tissue physiology.

机构信息

Department of Biomedical Engineering, The George Washington University, Washington DC, 20052, USA.

Department of Biomedical Engineering, The George Washington University, Washington DC, 20052, USA.

出版信息

Prog Biophys Mol Biol. 2019 Jul;144:139-150. doi: 10.1016/j.pbiomolbio.2018.06.001. Epub 2018 Jun 28.

Abstract

Human cardiac slices have emerged as a promising model of the human heart for scientific research and drug testing. Retaining the normal tissue architecture, a multi-cell type environment, and the native extracellular matrix, human cardiac slices faithfully replicate organ-level adult cardiac physiology. Previously, we demonstrated that human cardiac tissue slices cultured for 24 h maintained normal electrophysiology. In this project, we further optimized the organotypic culture condition to maintain normal electrophysiology of the human cardiac slices for 4 days. The prolonged culture of human cardiac tissue slices demonstrated here enables the study of chronic drug effects, gene therapies, and gene editing. To achieve greater control of the culture environment, we have also developed an automated, self-contained heart-on-a-chip system. The culture system supports media circulation, oxygenation, temperature control, electrical stimulation, and static mechanical loading. The culture parameters can be individually adjusted to establish the optimal culture condition to achieve long-term culture and to minimize tissue dedifferentiation. The development of the heart-on-a-chip technology presented here further encourages the use of organotypic human cardiac slices as a platform for pre-clinical drug testing and research in human cardiac physiology.

摘要

人心肌切片作为一种有前途的人类心脏模型,已经在科学研究和药物测试中得到了广泛应用。人心肌切片保留了正常的组织结构、多细胞类型的环境和天然的细胞外基质,可以真实地复制器官水平的成人心脏生理学。此前,我们已经证明,培养 24 小时的人心肌组织切片可以保持正常的电生理学特性。在本项目中,我们进一步优化了器官型培养条件,以维持人心肌切片的正常电生理学特性长达 4 天。这里展示的人心肌组织切片的长期培养使研究慢性药物作用、基因治疗和基因编辑成为可能。为了更好地控制培养环境,我们还开发了一种自动化、自给自足的芯片上心脏系统。该培养系统支持培养基循环、氧合、温度控制、电刺激和静态机械加载。可以单独调整培养参数,以建立最佳的培养条件,实现长期培养并最大限度地减少组织去分化。这里提出的芯片上心脏技术的发展进一步鼓励使用器官型人心肌切片作为临床前药物测试和人类心脏生理学研究的平台。

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