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基于水相双相Pickering乳液的原代内皮细胞和Hep-G2细胞的血管化共培养类聚集体

Vascularized Co-Culture Clusteroids of Primary Endothelial and Hep-G2 Cells Based on Aqueous Two-Phase Pickering Emulsions.

作者信息

Wang Anheng, Madden Leigh A, Paunov Vesselin N

机构信息

Department of Chemistry, University of Hull, Hull HU6 7RX, UK.

Department of Biomedical Sciences, University of Hull, Hull HU6 7RX, UK.

出版信息

Bioengineering (Basel). 2022 Mar 21;9(3):126. doi: 10.3390/bioengineering9030126.

Abstract

Three-dimensional cell culture has been extensively involved in biomedical applications due to its high availability and relatively mature biochemical properties. However, single 3D cell culture models based on hydrogel or various scaffolds do not meet the more in-depth requirements of in vitro models. The necrotic core formation inhibits the utilization of the 3D cell culture ex vivo as oxygen permeation is impaired in the absence of blood vessels. We report a simple method to facilitate the formation of angiogenic HUVEC (human umbilical vein endothelial cells) and Hep-G2 (hepatocyte carcinoma model) co-culture 3D clusteroids in a water-in-water (/) Pickering emulsions template which can overcome this limitation. This method enabled us to manipulate the cells proportion in order to achieve the optimal condition for stimulating the production of various angiogenic protein markers in the co-cultured clusteroids. The HUVEC cells respond to the presence of Hep-G2 cells and their byproducts by forming endothelial cell sprouts in Matrigel without the exogenous addition of vascular endothelial growth factor (VEGF) or other angiogenesis inducers. This culture method can be easily replicated to produce other types of cell co-culture spheroids. The / Pickering emulsion template can facilitate the fabrication of 3D co-culture models to a great extent and be further utilized in drug testing and tissue engineering applications.

摘要

由于其高可用性和相对成熟的生化特性,三维细胞培养已广泛应用于生物医学领域。然而,基于水凝胶或各种支架的单一三维细胞培养模型无法满足体外模型更深入的要求。坏死核心的形成抑制了三维细胞培养在体外的应用,因为在没有血管的情况下,氧气渗透会受到损害。我们报告了一种简单的方法,可在水包水(/)Pickering乳液模板中促进血管生成的人脐静脉内皮细胞(HUVEC)和肝癌细胞模型(Hep-G2)共培养三维类聚集体的形成,该方法可以克服这一限制。此方法使我们能够控制细胞比例,以达到刺激共培养类聚集体中各种血管生成蛋白标志物产生的最佳条件。在不额外添加血管内皮生长因子(VEGF)或其他血管生成诱导剂的情况下,HUVEC细胞通过在基质胶中形成内皮细胞芽来响应Hep-G2细胞及其副产物的存在。这种培养方法可以很容易地复制以产生其他类型的细胞共培养球体。/ Pickering乳液模板可以在很大程度上促进三维共培养模型的构建,并进一步用于药物测试和组织工程应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/521f/8945860/3ef5c2686f61/bioengineering-09-00126-g001.jpg

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