GenPhySE, Université de Toulouse, INRAE, ENVT, Castanet-Tolosan, 31326, France.
GABI, INRAE, AgroParisTech, Université Paris-Saclay, Jouy-en-Josas, 78350, France.
Vet Res. 2021 Feb 25;52(1):33. doi: 10.1186/s13567-021-00909-x.
In livestock species, the monolayer of epithelial cells covering the digestive mucosa plays an essential role for nutrition and gut barrier function. However, research on farm animal intestinal epithelium has been hampered by the lack of appropriate in vitro models. Over the past decade, methods to culture livestock intestinal organoids have been developed in pig, bovine, rabbit, horse, sheep and chicken. Gut organoids from farm animals are obtained by seeding tissue-derived intestinal epithelial stem cells in a 3-dimensional culture environment reproducing in vitro the stem cell niche. These organoids can be generated rapidly within days and are formed by a monolayer of polarized epithelial cells containing the diverse differentiated epithelial progeny, recapitulating the original structure and function of the native epithelium. The phenotype of intestinal organoids is stable in long-term culture and reflects characteristics of the digestive segment of origin. Farm animal intestinal organoids can be amplified in vitro, cryopreserved and used for multiple experiments, allowing an efficient reduction of the use of live animals for experimentation. Most of the studies using livestock intestinal organoids were used to investigate host-microbe interactions at the epithelial surface, mainly focused on enteric infections with viruses, bacteria or parasites. Numerous other applications of farm animal intestinal organoids include studies on nutrient absorption, genome editing and bioactive compounds screening relevant for agricultural, veterinary and biomedical sciences. Further improvements of the methods used to culture intestinal organoids from farm animals are required to replicate more closely the intestinal tissue complexity, including the presence of non-epithelial cell types and of the gut microbiota. Harmonization of the methods used to culture livestock intestinal organoids will also be required to increase the reproducibility of the results obtained in these models. In this review, we summarize the methods used to generate and cryopreserve intestinal organoids in farm animals, present their phenotypes and discuss current and future applications of this innovative culture system of the digestive epithelium.
在牲畜物种中,覆盖消化黏膜的单层上皮细胞对于营养和肠道屏障功能起着至关重要的作用。然而,由于缺乏适当的体外模型,对农场动物肠道上皮的研究受到了阻碍。在过去的十年中,已经开发了在猪、牛、兔、马、绵羊和鸡中培养家畜肠道类器官的方法。通过在 3 维培养环境中种植组织来源的肠道上皮干细胞,农场动物的肠道类器官可以在体外复制干细胞生态位,从而获得肠道类器官。这些类器官可以在几天内迅速产生,由单层极化的上皮细胞组成,其中包含各种分化的上皮祖细胞,重现了天然上皮的原始结构和功能。在长期培养中,肠道类器官的表型稳定,并反映了其起源的消化段的特征。农场动物的肠道类器官可以在体外扩增、冷冻保存并用于多次实验,从而有效地减少了活体动物实验的使用。使用家畜肠道类器官的大多数研究都用于研究上皮表面的宿主-微生物相互作用,主要集中在病毒、细菌或寄生虫引起的肠道感染上。农场动物肠道类器官的其他许多应用包括对营养吸收、基因组编辑和与农业、兽医和生物医学科学相关的生物活性化合物的筛选的研究。需要进一步改进用于培养农场动物肠道类器官的方法,以更紧密地复制肠道组织的复杂性,包括非上皮细胞类型和肠道微生物群的存在。还需要协调用于培养家畜肠道类器官的方法,以提高这些模型中获得的结果的可重复性。在这篇综述中,我们总结了用于生成和冷冻保存农场动物肠道类器官的方法,介绍了它们的表型,并讨论了这种创新的消化上皮培养系统的当前和未来应用。