All-aqueous droplets-templated tailorable core-shell alginate microspheres for constructing vascularized intestinal mucosa in vitro models.

IF 3.9 3区 医学 Q2 ENGINEERING, BIOMEDICAL Biomedical materials Pub Date : 2024-04-04 DOI:10.1088/1748-605X/ad3abc
Xin Hao, Ting Du, Feng Yang, Yilan Wang, Huatao He, Menghan Yang, Meiying Hong, Guanxiong Wang, Deqing Huang, Yaolei Wang
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Abstract

Recently, in vitro 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 relevant in vitro models of intestinal mucosa is the creation of three-dimensional (3D) 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 (ECM) 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 (HUVECs) 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 generating in vitro models of vascularized intestinal mucosa with epithelial and vascularized stroma arranged in a spatially relevant manner and demonstrating near-physiological functionality.
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用于构建血管化肠粘膜体外模型的全水滴-可定制核壳藻酸盐微球。
最近,肠粘膜体外模型已成为药物筛选和研究肠道生理与病理的重要工具。通过这些模型,可以研究细胞在疾病状态下的行为或对微环境改变的反应,有可能成为动物模型的替代品。构建与生理相关的体外肠粘膜模型的主要挑战之一是创建三维(3D)微结构,以准确模拟肠上皮和血管基质的整合。在这里,我们生成了核壳藻酸盐(Alg)微球,以创建模拟肠粘膜上皮和血管基质所需的分区细胞外基质(ECM)微环境。我们证明,嵌入微球核心的 NIH-3T3 和人脐静脉内皮细胞(HUVEC)可以增殖并形成血管网络,而人结肠直肠腺癌细胞(Caco-2)可以在外壳中形成上皮单层。与包裹在外壳内的 Caco-2 单层细胞相比,血管基质的存在能增强它们的增殖和功能。因此,我们的核壳 Alg 微球为体外生成血管化肠粘膜模型提供了一种有价值的方法,这种模型的上皮和血管化基质以空间相关的方式排列,并显示出接近生理的功能。
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来源期刊
Biomedical materials
Biomedical materials 工程技术-材料科学:生物材料
CiteScore
6.70
自引率
7.50%
发文量
294
审稿时长
3 months
期刊介绍: The goal of the journal is to publish original research findings and critical reviews that contribute to our knowledge about the composition, properties, and performance of materials for all applications relevant to human healthcare. Typical areas of interest include (but are not limited to): -Synthesis/characterization of biomedical materials- Nature-inspired synthesis/biomineralization of biomedical materials- In vitro/in vivo performance of biomedical materials- Biofabrication technologies/applications: 3D bioprinting, bioink development, bioassembly & biopatterning- Microfluidic systems (including disease models): fabrication, testing & translational applications- Tissue engineering/regenerative medicine- Interaction of molecules/cells with materials- Effects of biomaterials on stem cell behaviour- Growth factors/genes/cells incorporated into biomedical materials- Biophysical cues/biocompatibility pathways in biomedical materials performance- Clinical applications of biomedical materials for cell therapies in disease (cancer etc)- Nanomedicine, nanotoxicology and nanopathology- Pharmacokinetic considerations in drug delivery systems- Risks of contrast media in imaging systems- Biosafety aspects of gene delivery agents- Preclinical and clinical performance of implantable biomedical materials- Translational and regulatory matters
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