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全水相液滴模板化可定制的海藻酸钠核壳微球用于构建血管化的肠道黏膜模型。

All-aqueous droplets-templated tailorable core-shell alginate microspheres for constructing vascularized intestinal mucosamodels.

机构信息

School of Life Sciences and Engineering, Southwest Jiaotong University, Chengdu, Sichuan 610031, People's Republic of China.

School of Electrical Engineering, Southwest Jiaotong University, Chengdu 610031, People's Republic of China.

出版信息

Biomed Mater. 2024 Apr 26;19(3). doi: 10.1088/1748-605X/ad3abc.

DOI:10.1088/1748-605X/ad3abc
PMID:38574669
Abstract

Recently,models of intestinal mucosa have become important tools for drug screening and studying the physiology and pathology of the intestine. These models enable the examination of cellular behavior in diseased states or in reaction to alterations in the microenvironment, potentially serving as alternatives to animal models. One of the major challenges in constructing physiologically relevantmodels of intestinal mucosa is the creation of three-dimensional microstructures that accurately mimic the integration of intestinal epithelium and vascularized stroma. Here, core-shell alginate (Alg) microspheres were generated to create the compartmentalized extracellular matrix microenvironment needed to simulate the epithelial and vascularized stromal compartments of the intestinal mucosa. We demonstrated that NIH-3T3 and human umbilical vein endothelial cells embedded in the core of the microspheres can proliferate and develop a vascular network, while human colorectal adenocarcinoma cells (Caco-2) can form an epithelial monolayer in the shell. Compared to Caco-2 monolayer encapsulated within the shell, the presence of the vascularized stroma enhances their proliferation and functionality. As such, our core-shell Alg microspheres provide a valuable method for generatingmodels of vascularized intestinal mucosa with epithelial and vascularized stroma arranged in a spatially relevant manner and demonstrating near-physiological functionality.

摘要

最近,肠道黏膜模型已成为药物筛选和研究肠道生理学和病理学的重要工具。这些模型能够检查疾病状态或微环境改变下的细胞行为,可能成为动物模型的替代品。构建具有生理相关性的肠道黏膜模型的主要挑战之一是创建准确模拟肠道上皮和血管化基质整合的三维微结构。在这里,我们生成了核壳海藻酸钠(Alg)微球,以创建分隔的细胞外基质微环境,模拟肠道黏膜的上皮和血管化基质隔室。我们证明,包埋在微球核心内的 NIH-3T3 和人脐静脉内皮细胞可以增殖并形成血管网络,而人结直肠腺癌细胞(Caco-2)可以在壳层中形成上皮单层。与壳层内包被的 Caco-2 单层相比,血管化基质的存在增强了它们的增殖和功能。因此,我们的核壳 Alg 微球为生成具有以空间相关方式排列的上皮和血管化基质的血管化肠道黏膜模型提供了一种有价值的方法,并展示了接近生理的功能。

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