McGreevy Owen, Gilbert Timothy, Jessel Maria-Danae, Bosakhar Mohammed, Fenwick Stephen, Malik Hassan, Goldring Christopher, Randle Laura
University of Liverpool Department of Pharmacology and Therapeutics, Liverpool, England, UK.
Equal Contribution, Liverpool, UK.
F1000Res. 2025 Jun 10;14:571. doi: 10.12688/f1000research.162495.1. eCollection 2025.
Preclinical models vary in complexity and cost. Traditional 2D cell cultures that are high throughput and cost effective, but lack the complexity of multicellular interactions. Animal models and more complex, but are costly, raise ethical concerns and are not a human model to better understand human disease or response to novel treatments. Human precision cut tissue slice (hPCTS) models bridge this gap, maintaining the architecture and microenvironment of original tissues. This study examines the viability and functionality of hPCTS using different tissue culture formats. Previous studies have cultured hPCTS with gentle agitation, either on an insert or floating in tissue culture medium. More recently the use of a proprietary flow system for hPCTS culture has been explored, aiming to provide a more physiologically relevant environment. CELLBLOKS® provide a commercially available flow system platform designed for cell culture that we adapted to accommodate hPCTS. hPCTS were cultured for 15 days using an organotypic polytetrafluoroethylene Millicell insert, a CELLBLOKS® hydrophilic polyethylene terephthalate flow system plate or without an insert. Viability was assessed through MTS assays, while functionality was determined by measuring urea and albumin secretion across the 15 days in culture. The Millicell inserts maintained higher and more consistent viability and functionality over 15 days. Slices cultured with no inserts showed decreased viability and functionality after 7 days in culture. In contrast, CELLBLOKS® cultured hPCTS showed significantly decreased viability and function after 3 days in culture. This study suggests that while the CELLBLOKS® system shows promise for 2D cell line cultures, Millicell Biopore™ inserts offer a more reliable method for maintaining complex hPCTS cultures, preserving both viability and function. As a viable, human-specific alternative to animal models, hPCTS support the 3Rs and have the potential to reduced and potentially replace the use of animals in preclinical research, improving human disease modelling.
临床前模型在复杂性和成本方面各不相同。传统的二维细胞培养具有高通量且成本效益高,但缺乏多细胞相互作用的复杂性。动物模型更复杂,但成本高昂,引发伦理问题,且不是用于更好理解人类疾病或对新疗法反应的人类模型。人类精确切割组织切片(hPCTS)模型弥补了这一差距,保留了原始组织的结构和微环境。本研究使用不同的组织培养形式检查了hPCTS的活力和功能。先前的研究通过轻柔搅拌培养hPCTS,要么在插入物上,要么漂浮在组织培养基中。最近,人们探索了使用专有的流动系统进行hPCTS培养,旨在提供更具生理相关性的环境。CELLBLOKS®提供了一个专为细胞培养设计的商用流动系统平台,我们对其进行了改造以适应hPCTS。使用器官型聚四氟乙烯Millicell插入物、CELLBLOKS®亲水性聚对苯二甲酸乙二酯流动系统板或不使用插入物培养hPCTS 15天。通过MTS分析评估活力,同时通过测量培养15天期间的尿素和白蛋白分泌来确定功能。Millicell插入物在15天内保持了更高且更一致的活力和功能。无插入物培养的切片在培养7天后活力和功能下降。相比之下,CELLBLOKS®培养的hPCTS在培养3天后活力和功能显著下降。本研究表明,虽然CELLBLOKS®系统在二维细胞系培养方面显示出前景,但Millicell Biopore™插入物为维持复杂的hPCTS培养提供了一种更可靠的方法,既能保持活力又能保持功能。作为动物模型可行的、人类特异性的替代物,hPCTS支持3R原则,有潜力减少并可能取代临床前研究中动物的使用,改善人类疾病建模。