开发用于离散性主动脉瓣下狭窄的新型 3D Spheroids。

IF 1.6 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Sunita Brimmer, Pengfei Ji, Ravi K Birla, Jeffrey S Heinle, Jane K Grande-Allen, Sundeep G Keswani
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引用次数: 0

摘要

在这项研究中,我们提出了一种生物打印三维球体的新方法,用于研究被称为离散性主动脉瓣下狭窄(DSS)的复杂先天性心脏病。通过生物打印机,我们可以操纵挤出压力来改变球体的大小,藻酸盐孔隙率会随着时间的推移而增大。球体由人脐静脉内皮细胞(HUVECs)组成,我们证明了生物打印过程中的压力和时间可以调节球体的直径。此外,我们还使用了 Pluronic 酸来保持球体的形状和位置。对球体内 HUVEC 的表征证实了它们的均匀分布,我们还证明了细胞存活率与时间的函数关系。与传统的二维细胞培养相比,三维球形模型能提供更贴切的生理环境,因此在药物测试和治疗应用方面很有价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of Novel 3D Spheroids for Discrete Subaortic Stenosis.

In this study, we propose a new method for bioprinting 3D Spheroids to study complex congenital heart disease known as discrete subaortic stenosis (DSS). The bioprinter allows us to manipulate the extrusion pressure to change the size of the spheroids, and the alginate porosity increases in size over time. The spheroids are composed of human umbilical vein endothelial cells (HUVECs), and we demonstrated that pressure and time during the bioprinting process can modulate the diameter of the spheroids. In addition, we used Pluronic acid to maintain the shape and position of the spheroids. Characterization of HUVECs in the spheroids confirmed their uniform distribution and we demonstrated cell viability as a function of time. Compared to traditional 2D cell cultures, the 3D spheroids model provides more relevant physiological environments, making it valuable for drug testing and therapeutic applications.

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来源期刊
Cardiovascular Engineering and Technology
Cardiovascular Engineering and Technology Engineering-Biomedical Engineering
CiteScore
4.00
自引率
0.00%
发文量
51
期刊介绍: Cardiovascular Engineering and Technology is a journal publishing the spectrum of basic to translational research in all aspects of cardiovascular physiology and medical treatment. It is the forum for academic and industrial investigators to disseminate research that utilizes engineering principles and methods to advance fundamental knowledge and technological solutions related to the cardiovascular system. Manuscripts spanning from subcellular to systems level topics are invited, including but not limited to implantable medical devices, hemodynamics and tissue biomechanics, functional imaging, surgical devices, electrophysiology, tissue engineering and regenerative medicine, diagnostic instruments, transport and delivery of biologics, and sensors. In addition to manuscripts describing the original publication of research, manuscripts reviewing developments in these topics or their state-of-art are also invited.
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