Schumacher Michael A, Aihara Eitaro, Feng Rui, Engevik Amy, Shroyer Noah F, Ottemann Karen M, Worrell Roger T, Montrose Marshall H, Shivdasani Ramesh A, Zavros Yana
Department of Molecular and Cellular Physiology, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
J Physiol. 2015 Apr 15;593(8):1809-27. doi: 10.1113/jphysiol.2014.283028. Epub 2015 Feb 19.
An in vitro approach to study gastric development is primary mouse-derived epithelium cultured as three-dimensional spheroids known as organoids. We have devised two unique gastric fundic-derived organoid cultures: model 1 for the expansion of gastric fundic stem cells, and model 2 for the maintenance of mature cell lineages. Organoids maintained in co-culture with immortalized stomach mesenchymal cells express robust numbers of surface pit, mucous neck, chief, endocrine and parietal cells. Histamine induced a significant decrease in intraluminal pH that was reversed by omeprazole in fundic organoids and indicated functional activity and regulation of parietal cells. Localized photodamage resulted in rapid cell exfoliation coincident with migration of neighbouring cells to the damaged area, sustaining epithelial continuity. We report the use of these models for studies of epithelial cell biology and cell damage and repair.
Studies of gastric function and disease have been limited by the lack of extended primary cultures of the epithelium. An in vitro approach to study gastric development is primary mouse-derived antral epithelium cultured as three-dimensional spheroids known as organoids. There have been no reports on the use of organoids for gastric function. We have devised two unique gastric fundic-derived organoid cultures: model 1 for the expansion of gastric fundic stem cells, and model 2 for the maintenance of mature cell lineages. Both models were generated from single glands dissociated from whole fundic tissue and grown in basement membrane matrix (Matrigel) and organoid growth medium. Model 1 enriches for a stem cell-like niche via simple passage of the organoids. Maintained in Matrigel and growth medium, proliferating organoids expressed high levels of stem cell markers CD44 and Lgr5. Model 2 is a system of gastric organoids co-cultured with immortalized stomach mesenchymal cells (ISMCs). Organoids maintained in co-culture with ISMCs express robust numbers of surface pit, mucous neck, chief, endocrine and parietal cells. Histamine induced a significant decrease in intraluminal pH that was reversed by omeprazole in fundic organoids and indicated functional activity and regulation of parietal cells. Localized photodamage resulted in rapid cell exfoliation coincident with migration of neighbouring cells to the damaged area, sustaining epithelial continuity. Thus, we report the use of these models for studies of epithelial cell biology and cell damage and repair.
一种研究胃发育的体外方法是将源自小鼠的原代上皮培养成称为类器官的三维球体。我们设计了两种独特的源自胃底的类器官培养物:模型1用于胃底干细胞的扩增,模型2用于维持成熟细胞谱系。与永生化胃间充质细胞共培养的类器官表达大量的表面小凹、黏液颈、主细胞、内分泌细胞和壁细胞。组胺导致管腔内pH值显著降低,奥美拉唑可使其在胃底类器官中恢复,这表明壁细胞具有功能活性和调节作用。局部光损伤导致细胞迅速脱落,同时相邻细胞迁移至受损区域,维持上皮连续性。我们报告了使用这些模型来研究上皮细胞生物学以及细胞损伤和修复。
胃功能和疾病的研究一直受到上皮细胞原代培养无法长期维持的限制。一种研究胃发育的体外方法是将源自小鼠的胃窦上皮培养成称为类器官的三维球体。目前尚无关于类器官用于胃功能研究的报道。我们设计了两种独特的源自胃底的类器官培养物:模型1用于胃底干细胞的扩增,模型2用于维持成熟细胞谱系。这两种模型均由从整个胃底组织中分离出的单个腺体在基底膜基质(基质胶)和类器官生长培养基中培养而成。模型1通过简单传代类器官来富集类似干细胞的微环境。在基质胶和生长培养基中培养的增殖类器官表达高水平的干细胞标志物CD44和Lgr5。模型2是一个与永生化胃间充质细胞(ISMCs)共培养的胃类器官系统。与ISMCs共培养的类器官表达大量的表面小凹、黏液颈、主细胞、内分泌细胞和壁细胞。组胺导致管腔内pH值显著降低,奥美拉唑可使其在胃底类器官中恢复,这表明壁细胞具有功能活性和调节作用。局部光损伤导致细胞迅速脱落,同时相邻细胞迁移至受损区域,维持上皮连续性。因此,我们报告了使用这些模型来研究上皮细胞生物学以及细胞损伤和修复。