Purdue University, Department of Basic Medical Sciences, 625 Harrison Street, West Lafayette, IN 47907, USA; 3D Cell Culture Core (3D3C) Facility, Birck Nanotechnology Center, Purdue University Discovery Park, 1205 West State Street, West Lafayette, IN 47907, USA; Purdue University Center for Cancer Research, 201 S University Street, West Lafayette, IN 47907, USA.
3D Cell Culture Core (3D3C) Facility, Birck Nanotechnology Center, Purdue University Discovery Park, 1205 West State Street, West Lafayette, IN 47907, USA.
Toxicol In Vitro. 2017 Dec;45(Pt 3):287-295. doi: 10.1016/j.tiv.2017.03.012. Epub 2017 Mar 30.
Three-dimensional cell culture has the potential to revolutionize toxicology studies by allowing human-based reproduction of essential elements of organs. Beyond the study of toxicants on the most susceptible organs such as liver, kidney, skin, lung, gastrointestinal tract, testis, heart and brain, carcinogenesis research will also greatly benefit from 3D cell culture models representing any normal tissue. No tissue function can be suitably reproduced without the appropriate tissue architecture whether mimicking acini, ducts or tubes, sheets of cells or more complex cellular organizations like hepatic cords. In this review, we illustrate the fundamental characteristics of polarity that is an essential architectural feature of organs for which different 3D cell culture models are available for toxicology studies in vitro. The value of tissue polarity for the development of more accurate carcinogenesis studies is also exemplified, and the concept of using extracellular gradients of gaseous or chemical substances produced with microfluidics in 3D cell culture is discussed. Indeed such gradients-on-a-chip might bring unprecedented information to better determine permissible exposure levels. Finally, the impact of tissue architecture, established via cell-matrix interactions, on the cell nucleus is emphasized in light of the importance in toxicology of morphological and epigenetic alterations of this organelle.
三维细胞培养有可能通过允许基于人体的器官基本元素的再现来彻底改变毒理学研究。除了研究肝脏、肾脏、皮肤、肺、胃肠道、睾丸、心脏和大脑等最易受影响的器官上的毒物外,致癌研究也将极大地受益于代表任何正常组织的 3D 细胞培养模型。没有适当的组织架构,任何组织功能都无法得到适当的再现,无论是模拟腺泡、导管还是管、细胞片层还是更复杂的细胞组织,如肝索。在这篇综述中,我们说明了极性的基本特征,极性是器官的一个基本结构特征,为此,已经有不同的 3D 细胞培养模型可用于体外毒理学研究。还举例说明了组织极性对于发展更准确的致癌研究的价值,并讨论了使用微流控技术在 3D 细胞培养中产生的气态或化学物质的细胞外梯度的概念。事实上,这种芯片上的梯度可能会带来前所未有的信息,以更好地确定可允许的暴露水平。最后,鉴于细胞器形态和表观遗传改变在毒理学中的重要性,强调了细胞-基质相互作用建立的组织架构对细胞核的影响。