Fernando Elizabeth H, Dicay Michael, Stahl Martin, Gordon Marilyn H, Vegso Andrew, Baggio Cristiane, Alston Laurie, Lopes Fernando, Baker Kristi, Hirota Simon, McKay Derek M, Vallance Bruce, MacNaughton Wallace K
Department of Physiology and Pharmacology and Gastrointestinal Research Group, University of Calgary, Calgary, Alberta, Canada.
Department of Pediatrics, British Columbia Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada; and.
Am J Physiol Gastrointest Liver Physiol. 2017 Nov 1;313(5):G467-G475. doi: 10.1152/ajpgi.00152.2017. Epub 2017 Jul 27.
Cancer cell lines have been the mainstay of intestinal epithelial experimentation for decades, due primarily to their immortality and ease of culture. However, because of the inherent biological abnormalities of cancer cell lines, many cellular biologists are currently transitioning away from these models and toward more representative primary cells. This has been particularly challenging, but recent advances in the generation of intestinal organoids have brought the routine use of primary cells within reach of most epithelial biologists. Nevertheless, even with the proliferation of publications that use primary intestinal epithelial cells, there is still a considerable amount of trial and error required for laboratories to establish a consistent and reliable method to culture three-dimensional (3D) intestinal organoids and primary epithelial monolayers. We aim to minimize the time other laboratories spend troubleshooting the technique and present a standard method for culturing primary epithelial cells. Therefore, we have described our optimized, high-yield, cost-effective protocol to grow 3D murine colonoids for more than 20 passages and our detailed methods to culture these cells as confluent monolayers for at least 14 days, enabling a wide variety of potential future experiments. By supporting and expanding on the current literature of primary epithelial culture optimization and detailed use in experiments, we hope to help enable the widespread adoption of these innovative methods and allow consistency of results obtained across laboratories and institutions. Primary intestinal epithelial monolayers are notoriously difficult to maintain culture, even with the recent advances in the field. We describe, in detail, the protocols required to maintain three-dimensional cultures of murine colonoids and passage these primary epithelial cells to confluent monolayers in a standardized, high-yield and cost-effective manner.
几十年来,癌细胞系一直是肠道上皮实验的主要支柱,这主要归功于它们的永生性和易于培养的特性。然而,由于癌细胞系固有的生物学异常,许多细胞生物学家目前正从这些模型转向更具代表性的原代细胞。这一直是一项特别具有挑战性的任务,但肠道类器官生成方面的最新进展使大多数上皮生物学家能够常规使用原代细胞。尽管如此,即使使用原代肠道上皮细胞的出版物不断增加,实验室仍需要大量的反复试验,才能建立一种一致且可靠的方法来培养三维(3D)肠道类器官和原代上皮单层细胞。我们的目标是尽量减少其他实验室在该技术故障排除上花费的时间,并提出一种培养原代上皮细胞的标准方法。因此,我们描述了我们优化的、高产的、具有成本效益的方案,用于培养3D小鼠结肠类器官超过20代,以及我们将这些细胞培养成汇合单层细胞至少14天的详细方法,从而实现各种潜在的未来实验。通过支持和扩展当前关于原代上皮细胞培养优化及在实验中的详细应用的文献,我们希望有助于这些创新方法的广泛采用,并使不同实验室和机构获得的结果具有一致性。即使该领域最近取得了进展,原代肠道上皮单层细胞的培养仍然非常困难。我们详细描述了维持小鼠结肠类器官三维培养以及将这些原代上皮细胞传代至汇合单层细胞所需的标准化、高产且具有成本效益的方案。