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通过快速细胞间点击组装过程生成无支架三维肝组织。

Generation of a Scaffold-Free Three-Dimensional Liver Tissue via a Rapid Cell-to-Cell Click Assembly Process.

作者信息

Rogozhnikov Dmitry, Luo Wei, Elahipanah Sina, O'Brien Paul J, Yousaf Muhammad N

机构信息

Department of Chemistry and Biology, York University , Toronto, Ontario M3J 1P3, Canada.

OrganoLinX Inc. , Toronto, Ontario M3J 1P3, Canada.

出版信息

Bioconjug Chem. 2016 Sep 21;27(9):1991-8. doi: 10.1021/acs.bioconjchem.6b00187. Epub 2016 Aug 10.

Abstract

There has been tremendous interest in constructing in vitro liver organ models for a range of fundamental studies of cell signaling, metabolism, and infectious diseases, and as a commercial system to evaluate therapeutic drug discovery prioritization and toxicity. Although there has been progress toward studying two-dimensional hepatic function in vitro, there remain challenging obstacles to generate rapid and efficient scaffold-free three-dimensional multiple cell line coculture tissue models of liver. Herein, we develop and employ a strategy to induce specific and stable cell-cell contacts among multiple hepatic cell lines to generate 3D tissues through cell-surface engineering based on liposome delivery and fusion to display bio-orthogonal functional groups from cell membranes. We generate, for the first time, a three cell line coculture 3D liver tissue model by assembling hepatocytes, hepatic endothelial cells, and hepatic stellate cells via a rapid intercell click ligation process. We compare and analyze the function of the superior 3D liver tissue chips with 2D coculture monolayer by assessing mitochondrial metabolic activity and evaluating drug toxicity.

摘要

构建体外肝脏器官模型用于细胞信号传导、新陈代谢和传染病等一系列基础研究,并作为评估治疗药物发现优先级和毒性的商业系统,已引起了极大的关注。尽管在体外研究二维肝功能方面已取得进展,但要生成快速高效的无支架三维多细胞系共培养肝脏组织模型仍存在具有挑战性的障碍。在此,我们开发并采用了一种策略,通过基于脂质体递送和融合的细胞表面工程,在多个肝细胞系之间诱导特异性和稳定的细胞间接触,以展示细胞膜上的生物正交官能团,从而生成三维组织。我们首次通过快速的细胞间点击连接过程组装肝细胞、肝内皮细胞和肝星状细胞,生成了三细胞系共培养三维肝脏组织模型。我们通过评估线粒体代谢活性和评价药物毒性,比较并分析了优质三维肝脏组织芯片与二维共培养单层的功能。

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