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β-发夹水凝胶作为三维细胞培养中高通量药物发现的支架。

Beta-hairpin hydrogels as scaffolds for high-throughput drug discovery in three-dimensional cell culture.

作者信息

Worthington Peter, Drake Katherine M, Li Zhiqin, Napper Andrew D, Pochan Darrin J, Langhans Sigrid A

机构信息

Nemours Center for Childhood Cancer Research, Alfred I. duPont Hospital for Children, Wilmington, DE 19803, USA; Department of Biomedical Engineering, University of Delaware, Newark, DE 19716, USA.

Nemours Center for Childhood Cancer Research, Alfred I. duPont Hospital for Children, Wilmington, DE 19803, USA.

出版信息

Anal Biochem. 2017 Oct 15;535:25-34. doi: 10.1016/j.ab.2017.07.024. Epub 2017 Jul 27.

DOI:10.1016/j.ab.2017.07.024
PMID:28757092
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5576559/
Abstract

Automated cell-based high-throughput screening (HTS) is a powerful tool in drug discovery, and it is increasingly being recognized that three-dimensional (3D) models, which more closely mimic in vivo-like conditions, are desirable screening platforms. One limitation hampering the development of 3D HTS is the lack of suitable 3D culture scaffolds that can readily be incorporated into existing HTS infrastructure. We now show that β-hairpin peptide hydrogels can serve as a 3D cell culture platform that is compatible with HTS. MAX8 β-hairpin peptides can physically assemble into a hydrogel with defined porosity, permeability and mechanical stability with encapsulated cells. Most importantly, the hydrogels can then be injected under shear-flow and immediately reheal into a hydrogel with the same properties exhibited prior to injection. The post-injection hydrogels are cell culture compatible at physiological conditions. Using standard HTS equipment and medulloblastoma pediatric brain tumor cells as a model system, we show that automatic distribution of cell-peptide mixtures into 384-well assay plates results in evenly dispensed, viable MAX8-cell constructs suitable for commercially available cell viability assays. Since MAX8 peptides can be functionalized to mimic the microenvironment of cells from a variety of origins, MAX8 peptide gels should have broad applicability for 3D HTS drug discovery.

摘要

基于细胞的自动化高通量筛选(HTS)是药物发现中的一种强大工具,并且越来越多的人认识到,更接近体内样条件的三维(3D)模型是理想的筛选平台。阻碍3D HTS发展的一个限制因素是缺乏能够轻松整合到现有HTS基础设施中的合适3D培养支架。我们现在表明,β-发夹肽水凝胶可以作为一种与HTS兼容的3D细胞培养平台。MAX8 β-发夹肽可以物理组装成具有确定孔隙率、渗透率和机械稳定性的水凝胶,并包裹细胞。最重要的是,然后可以在剪切流下注射水凝胶,并且它会立即重新愈合为具有注射前相同性质的水凝胶。注射后的水凝胶在生理条件下与细胞培养兼容。使用标准的HTS设备并以小儿髓母细胞瘤脑肿瘤细胞作为模型系统,我们表明将细胞-肽混合物自动分配到384孔测定板中会产生均匀分布、适合商业可用细胞活力测定的有活力的MAX8-细胞构建体。由于MAX8肽可以被功能化以模拟来自各种来源的细胞的微环境,MAX8肽凝胶在3D HTS药物发现中应该具有广泛的适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1851/5576559/16675b161d4b/nihms897735f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1851/5576559/e1bd999872be/nihms897735f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1851/5576559/3635a5397fa2/nihms897735f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1851/5576559/0b8af35a0803/nihms897735f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1851/5576559/16675b161d4b/nihms897735f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1851/5576559/e1bd999872be/nihms897735f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1851/5576559/3635a5397fa2/nihms897735f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1851/5576559/0b8af35a0803/nihms897735f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1851/5576559/16675b161d4b/nihms897735f4.jpg

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本文引用的文献

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Sustained release of active chemotherapeutics from injectable-solid β-hairpin peptide hydrogel.活性化疗药物从可注射固体β-发夹肽水凝胶中的持续释放。
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