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使用新型无自由基微流控系统在柔软各向异性聚乙二醇微凝胶中进行细胞包封。

Cell Encapsulation in Soft, Anisometric Poly(ethylene) Glycol Microgels Using a Novel Radical-Free Microfluidic System.

机构信息

DWI-Leibniz Institute for Interactive Materials, Forckenbeckstrasse 50, 52074, Aachen, Germany.

AVT.CVT, Forckenbeckstrasse 51, 52074, Aachen, Germany.

出版信息

Small. 2019 May;15(20):e1900692. doi: 10.1002/smll.201900692. Epub 2019 Apr 16.

Abstract

Complex 3D artificial tissue constructs are extensively investigated for tissue regeneration. Frequently, materials and cells are delivered separately without benefitting from the synergistic effect of combined administration. Cell delivery inside a material construct provides the cells with a supportive environment by presenting biochemical, mechanical, and structural signals to direct cell behavior. Conversely, the cell/material interaction is poorly understood at the micron scale and new systems are required to investigate the effect of micron-scale features on cell functionality. Consequently, cells are encapsulated in microgels to avoid diffusion limitations of nutrients and waste and facilitate analysis techniques of single or collective cells. However, up to now, the production of soft cell-loaded microgels by microfluidics is limited to spherical microgels. Here, a novel method is presented to produce monodisperse, anisometric poly(ethylene) glycol microgels to study cells inside an anisometric architecture. These microgels can potentially direct cell growth and can be injected as rod-shaped mini-tissues that further assemble into organized macroscopic and macroporous structures post-injection. Their aspect ratios are adjusted with flow parameters, while mechanical and biochemical properties are altered by modifying the precursors. Encapsulated primary fibroblasts are viable and spread and migrate across the 3D microgel structure.

摘要

复杂的 3D 人工组织构建体被广泛研究用于组织再生。通常,材料和细胞是分开递送的,而没有受益于联合给药的协同效应。将细胞递送到材料构建体内部通过向细胞提供生物化学、机械和结构信号来为细胞提供支持环境,以指导细胞行为。相反,细胞/材料相互作用在微米尺度上的理解很差,需要新的系统来研究微米尺度特征对细胞功能的影响。因此,细胞被包封在微凝胶中以避免营养物质和废物的扩散限制,并促进单细胞或细胞群体的分析技术。然而,到目前为止,通过微流控技术生产软细胞负载的微凝胶仅限于球形微凝胶。在这里,提出了一种新的方法来生产单分散的各向异性聚乙二醇微凝胶,以研究各向异性结构中的细胞。这些微凝胶可以潜在地指导细胞生长,并可以作为棒状的迷你组织注入,进一步在注入后组装成有组织的宏观和大孔结构。它们的纵横比可以通过流动参数来调节,而机械和生化性质可以通过改变前体来改变。包封的原代成纤维细胞是存活的,并在 3D 微凝胶结构中扩散和迁移。

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