AvantiCell Science Ltd, GibbsYard Building, Auchincruive, KA6 5HW Ayr, Scotland, UK.
AvantiCell Science Ltd, GibbsYard Building, Auchincruive, KA6 5HW Ayr, Scotland, UK.
Toxicol In Vitro. 2019 Dec;61:104606. doi: 10.1016/j.tiv.2019.104606. Epub 2019 Jul 22.
Three-dimensional (3D) colon organoids, termed "colonoids", derived from adult stem cells represent a powerful tool in in vitro pharmaceutical and toxicological research. Murine and human colonoid models exist. Here we describe the establishment of bovine colonoids for agri-biotechnological applications, and extend the repertoire of colonoid culture options through proof-of-principle for bioprinting and novel in-plate cryopreservation technology. As a first step, we differentiated established long-term bovine colonoid cultures into mature colonoids. Tissue-specific differentiation was demonstrated by gene expression. Second, we investigated cryopreservation of colonoids in situ within an extracellular matrix in multi-well plates. Upon controlled thawing, cryopreserved 3D cultures grew at similar rates to unfrozen colonoids. Cytotoxic sensitivity to staurosporine was not significantly different between in situ freeze-thawed and unfrozen control cultures. Third, scalability of colonoid culture assembly by extrusion bioprinting into multi-well plates using GelMA bioink was assessed. With optimised bioprinting and crosslinking parameters, colonoids in GelMA were printed into 96 well culture plates and remained viable and proliferative post-print. For tissue-relevant in vitro studies we furthermore established differentiated colonoid-derived monolayer cultures on permeable membranes. Taken together, we outline novel in vitro approaches to study the ruminant colonic epithelium and introduce in-plate cryopreservation as convenient alternative to conventional in-vial cryopreservation.
三维(3D)结肠类器官,称为“类器官”,来源于成体干细胞,是体外药物和毒理学研究的有力工具。存在鼠和人类的类器官模型。在这里,我们描述了牛类器官的建立,用于农业生物技术应用,并通过生物打印和新型板内冷冻保存技术的原理验证扩展了类器官培养方案的范围。作为第一步,我们将已建立的长期牛类器官培养物分化为成熟的类器官。通过基因表达证明了组织特异性分化。其次,我们研究了在多孔板中的细胞外基质中对类器官进行原位冷冻保存。在受控解冻后,冷冻保存的 3D 培养物以与未冷冻类器官相似的速度生长。与未冷冻对照培养物相比,原位冷冻解冻的类器官对 staurosporine 的细胞毒性敏感性没有显着差异。第三,通过使用 GelMA 生物墨水在多孔板中挤出生物打印来评估类器官培养物组装的可扩展性。通过优化的生物打印和交联参数,可以将 GelMA 中的类器官打印到 96 孔培养板中,并且在打印后仍保持存活和增殖。对于与组织相关的体外研究,我们还在可渗透膜上建立了分化的类器官衍生的单层培养物。总之,我们概述了研究反刍动物结肠上皮的新型体外方法,并介绍了板内冷冻保存作为传统管内冷冻保存的便捷替代方法。