Lee Seung Bum, Han Sung-Hoon, Park Sunhoo
Laboratory of Radiation Exposure & Therapeutics, National Radiation Emergency Medical Center, Korea Institute of Radiological and Medical Science, Seoul, Republic of Korea.
Methods Mol Biol. 2018;1817:123-135. doi: 10.1007/978-1-4939-8600-2_13.
The in vitro long-term expansion of primary intestinal epithelial cells has been hampered by the inability to maintain an immature stem cell population. Recent technical advances have led to the development of a novel in vitro culture system that can sustain intestinal stem cells (ISCs) using growth factors that mimic the intestinal microenvironment in combination with a three-dimensional (3D) culture. The resulting intestinal organoids display a crypt-villus architecture that recapitulates the native intestinal epithelium. Here, we describe our method for the long-term culture of intestinal epithelial organoids via consistent passaging using a gentle cell dissociation reagent to easily break the organoid into smaller pieces. The long-term cryopreservation and defining characteristics of these intestinal organoids also make this work relevant for the advancement of epithelial organoid-based therapeutic technologies by allowing the production of large numbers of cells for use in clinical applications.
原代肠上皮细胞的体外长期扩增一直受到无法维持未成熟干细胞群体的阻碍。最近的技术进步促成了一种新型体外培养系统的开发,该系统可以使用模拟肠道微环境的生长因子结合三维(3D)培养来维持肠道干细胞(ISC)。由此产生的肠道类器官呈现出隐窝 - 绒毛结构,重现了天然肠上皮。在这里,我们描述了一种通过使用温和的细胞解离试剂进行连续传代来长期培养肠上皮类器官的方法,该试剂可轻松将类器官分解成更小的碎片。这些肠道类器官的长期冷冻保存及其明确特征也使得这项工作与基于上皮类器官的治疗技术的进步相关,因为它能够产生大量细胞用于临床应用。