Department of Internal Medicine, Division of Gastroenterology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Center for Cell Plasticity and Organ Design, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Development. 2022 Oct 15;149(20). doi: 10.1242/dev.200614. Epub 2022 Oct 24.
Many esophageal diseases can arise during development or throughout life. Therefore, well-characterized in vitro models and detailed methods are essential for studying human esophageal development, homeostasis and disease. Here, we (1) create an atlas of the cell types observed in the normal adult human esophagus; (2) establish an ancestrally diverse biobank of in vitro esophagus tissue to interrogate homeostasis and injury; and (3) benchmark in vitro models using the adult human esophagus atlas. We created a single-cell RNA sequencing reference atlas using fresh adult esophagus biopsies and a continuously expanding biobank of patient-derived in vitro cultures (n=55 lines). We identify and validate several transcriptionally distinct cell classes in the native human adult esophagus, with four populations belonging to the epithelial layer, including basal, epibasal, early differentiating and terminally differentiated luminal cells. Benchmarking in vitro esophagus cultures to the in vivo reference using single-cell RNA sequencing shows that the basal stem cells are robustly maintained in vitro, and the diversity of epithelial cell types in culture is dependent on cell density. We also demonstrate that cultures can be grown in 2D or as 3D organoids, and these methods can be employed for modeling the complete epithelial layers, thereby enabling in vitro modeling of the human adult esophagus.
许多食管疾病可能在发育过程中或一生中出现。因此,研究人类食管发育、稳态和疾病需要具有良好特征的体外模型和详细的方法。在这里,我们:(1) 绘制了正常成人食管中观察到的细胞类型图谱;(2) 建立了一个具有多种祖先的体外食管组织生物库,以研究稳态和损伤;(3) 使用成人食管图谱来评估体外模型。我们使用新鲜的成人食管活检和不断扩大的患者衍生的体外培养物生物库(n=55 株)创建了一个单细胞 RNA 测序参考图谱。我们在天然人成年食管中鉴定并验证了几个转录上不同的细胞类群,其中四个群体属于上皮层,包括基底、上皮基底、早期分化和终末分化的腔细胞。使用单细胞 RNA 测序将体外食管培养物与体内参考进行基准测试表明,体外培养物中基底干细胞得到了很好的维持,并且培养物中上皮细胞类型的多样性取决于细胞密度。我们还证明,培养物可以在 2D 或 3D 类器官中生长,这些方法可用于模拟完整的上皮层,从而实现人类成年食管的体外建模。