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3D 体外细胞和外植体在类液体固体中的培养平台。

3D In Vitro Platform for Cell and Explant Culture in Liquid-like Solids.

机构信息

Department of Mechanical and Aerospace Engineering, University of Florida, Gainesville, FL 32611, USA.

Division of Pulmonary, Critical Care, and Sleep Medicine, University of Florida, Gainesville, FL 32611, USA.

出版信息

Cells. 2022 Mar 11;11(6):967. doi: 10.3390/cells11060967.

Abstract

Existing 3D cell models and technologies have offered tools to elevate cell culture to a more physiologically relevant dimension. One mechanism to maintain cells cultured in 3D is by means of perfusion. However, existing perfusion technologies for cell culture require complex electronic components, intricate tubing networks, or specific laboratory protocols for each application. We have developed a cell culture platform that simply employs a pump-free suction device to enable controlled perfusion of cell culture media through a bed of granular microgels and removal of cell-secreted metabolic waste. We demonstrated the versatile application of the platform by culturing single cells and keeping tissue microexplants viable for an extended period. The human cardiomyocyte AC16 cell line cultured in our platform revealed rapid cellular spheroid formation after 48 h and ~90% viability by day 7. Notably, we were able to culture gut microexplants for more than 2 weeks as demonstrated by immunofluorescent viability assay and prolonged contractility.

摘要

现有的 3D 细胞模型和技术为提高细胞培养的生理相关性提供了工具。维持 3D 培养细胞的一种机制是通过灌流。然而,现有的细胞培养灌流技术需要复杂的电子元件、复杂的管道网络或针对每个应用的特定实验室方案。我们开发了一种细胞培养平台,它仅使用无泵抽吸装置来实现通过颗粒微凝胶床的受控细胞培养基灌流和细胞分泌的代谢废物的去除。我们通过培养单细胞和使组织微组织保持活力来证明该平台的多功能应用,延长了一段时间。在我们的平台中培养的人类心肌细胞 AC16 系在 48 小时后迅速形成细胞球体,第 7 天的活力约为 90%。值得注意的是,我们能够培养肠道微组织超过 2 周,通过免疫荧光活力测定和延长的收缩性来证明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b230/8946834/cdf69e152151/cells-11-00967-g001.jpg

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