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用于肝脏组织工程的水凝胶整合式生物芯片

Cryogel-Integrated Biochip for Liver Tissue Engineering.

机构信息

Université de Technologie de Compiègne, UMR CNRS 7338 Biomécanique et Bioingénierie, Centre de Recherche de Royallieu, Compiègne 60203, France.

Department of Chemical Engineering, Northeastern University, Boston, Massachusetts 02115-5005, United States.

出版信息

ACS Appl Bio Mater. 2021 Jul 19;4(7):5617-5626. doi: 10.1021/acsabm.1c00425. Epub 2021 Jul 8.

Abstract

Microfluidic systems and polymer hydrogels have been widely developed for tissue engineering. Yet, only a few tools combining both approaches, especially for liver models, are being explored. In this study, an alginate-based cryogel-integrated biochip was engineered for dynamic hepatoma cell line culture in three dimensions (3D). The alginate cryogel was covalently cross-linked in the biochip at subzero temperatures ( < 0 °C) to create a scaffold with high mechanical stability and an interconnected macroporous network. By varying the alginate concentration and the cross-linker ratio, Young's modulus of the cryogel can be fine-tuned between 1.5 and 29 kPa, corresponding to the range of stiffness of the different physiological states of the liver. We demonstrated that HepG2/C3A cells can be cultured and maintained as viable under dynamic conditions in this device up to 6 days. Albumin synthesis and glucose consumption increased over the cell culture days. Moreover, a 3D cell structure was observed across the entire height of the biochip, which was preserved following alginate lyase treatment to remove the cryogel-based scaffold. In summary, these results represent a proof of concept of an interesting cell culture technology that should be further investigated to engineer healthy and cirrhotic liver models.

摘要

微流控系统和聚合物水凝胶已广泛应用于组织工程领域。然而,将这两种方法结合起来的工具,特别是用于肝模型的工具,仍在探索之中。在这项研究中,我们设计了一种基于海藻酸盐的冷冻凝胶集成生物芯片,用于肝癌细胞系在三维(3D)环境中的动态培养。海藻酸盐冷冻凝胶在生物芯片中于亚低温(<0°C)下进行共价交联,形成具有高机械稳定性和互连通大孔网络的支架。通过改变海藻酸盐浓度和交联剂比例,可以将冷冻凝胶的杨氏模量精细调节在 1.5 至 29 kPa 之间,这对应于肝脏不同生理状态的硬度范围。我们证明了 HepG2/C3A 细胞可以在该设备中动态培养并保持活力,培养时间长达 6 天。白蛋白合成和葡萄糖消耗在整个细胞培养过程中增加。此外,在整个生物芯片高度上观察到了 3D 细胞结构,在用海藻酸盐裂解酶处理以去除基于冷冻凝胶的支架后,该结构得以保留。总之,这些结果代表了一种有趣的细胞培养技术的概念验证,应该进一步研究以构建健康和肝硬化的肝模型。

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