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基于重力的流动高效灌注培养系统用于模拟肝脏炎症的球体

Gravity-Based Flow Efficient Perfusion Culture System for Spheroids Mimicking Liver Inflammation.

作者信息

Kim Young-Su, Asif Arun, Chethikkattuveli Salih Abdul Rahim, Lee Jae-Wook, Hyun Ki-Nam, Choi Kyung-Hyun

机构信息

BioSpero Inc., Jeju-si 63243, Jeju-do, Korea.

Advanced Micro Mechatronics Lab, Department of Mechatronics Engineering, Jeju National University, Jeju-si 63243, Jeju-do, Korea.

出版信息

Biomedicines. 2021 Oct 1;9(10):1369. doi: 10.3390/biomedicines9101369.

Abstract

The spheroid culture system provides an efficient method to emulate organ-specific pathophysiology, overcoming the traditional two-dimensional (2D) cell culture limitations. The intervention of microfluidics in the spheroid culture platform has the potential to enhance the capacity of in vitro microphysiological tissues for disease modeling. Conventionally, spheroid culture is carried out in static conditions, making the media nutrient-deficient around the spheroid periphery. The current approach tries to enhance the capacity of the spheroid culture platform by integrating the perfusion channel for dynamic culture conditions. A pro-inflammatory hepatic model was emulated using a coculture of HepG2 cell line, fibroblasts, and endothelial cells for validating the spheroid culture plate with a perfusable channel across the spheroid well. Enhanced proliferation and metabolic capacity of the microphysiological model were observed and further validated by metabolic assays. A comparative analysis of static and dynamic conditions validated the advantage of spheroid culture with dynamic media flow. Hepatic spheroids were found to have improved proliferation in dynamic flow conditions as compared to the static culture platform. The perfusable culture system for spheroids is more physiologically relevant as compared to the static spheroid culture system for disease and drug analysis.

摘要

球体培养系统提供了一种模拟器官特异性病理生理学的有效方法,克服了传统二维(2D)细胞培养的局限性。微流体技术介入球体培养平台,有可能增强体外微生理组织用于疾病建模的能力。传统上,球体培养是在静态条件下进行的,这使得球体周边的培养基营养不足。当前的方法试图通过整合灌注通道以实现动态培养条件,来提高球体培养平台的能力。使用HepG2细胞系、成纤维细胞和内皮细胞的共培养来模拟促炎性肝脏模型,以验证具有贯穿球体孔的可灌注通道的球体培养板。观察到微生理模型的增殖和代谢能力增强,并通过代谢测定进一步验证。对静态和动态条件的比较分析验证了动态培养基流动下球体培养的优势。与静态培养平台相比,发现肝脏球体在动态流动条件下增殖有所改善。与用于疾病和药物分析的静态球体培养系统相比,用于球体的可灌注培养系统在生理上更具相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2ad/8533112/fa15aabef29b/biomedicines-09-01369-g001.jpg

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