Department of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Department of Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.
J Pathol. 2019 Jun;248(2):179-190. doi: 10.1002/path.5244. Epub 2019 Feb 20.
In the mammalian stomach, the isthmus has been considered as a stem cell zone. However, various locations and proliferative activities of gastric stem cells have been reported. We focused here on the stem cell marker Bmi1, a polycomb group protein, aiming to elucidate the characteristics of Bmi1-expressing cells in the stomach and to examine their stem cell potential. We investigated the Bmi1-expressing cell lineage in Bmi1-CreERT; Rosa26-YFP, LacZ or Rosa26-Confetti mice. We examined the in vivo and ex vivo effects of Bmi1-expressing cell ablation by using Bmi1-CreERT; Rosa26-iDTR mice. The Bmi1 lineage was also traced during regeneration after high-dose tamoxifen-, irradiation- and acetic acid-induced mucosal injuries. In the lineage-tracing experiments using low-dose tamoxifen, Bmi1-expressing cells in the isthmus of the gastric antrum and corpus provided progeny bidirectionally, towards both the luminal and basal sides over 6 months. In gastric organoids, Bmi1-expressing cells also provided progeny. Ablation of Bmi1-expressing cells resulted in impaired gastric epithelium in both mouse stomach and organoids. After high-dose tamoxifen-induced gastric mucosal injury, Bmi1-expressing cell lineages expanded and fully occupied all gastric glands of the antrum and the corpus within 7 days after tamoxifen injection. After irradiation- and acetic acid-induced gastric mucosal injuries, Bmi1-expressing cells also contributed to regeneration. In conclusion, Bmi1 is a gastric stem cell marker expressed in the isthmus of the antrum and corpus. Bmi1-expressing cells have stem cell potentials, both under physiological conditions and during regeneration after gastric mucosal injuries. Copyright © 2019 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
在哺乳动物的胃中,峡部被认为是干细胞区。然而,已经报道了各种位置和胃干细胞的增殖活性。我们在这里重点关注多梳组蛋白 Bmi1 这一干细胞标志物,旨在阐明胃中 Bmi1 表达细胞的特征,并研究其干细胞潜能。我们在 Bmi1-CreERT;Rosa26-YFP、LacZ 或 Rosa26-Confetti 小鼠中研究了 Bmi1 表达细胞谱系。我们使用 Bmi1-CreERT;Rosa26-iDTR 小鼠研究了 Bmi1 表达细胞消融的体内和体外效应。在高剂量他莫昔芬、照射和乙酸诱导的黏膜损伤后的再生过程中,我们还追踪了 Bmi1 谱系。在使用低剂量他莫昔芬的谱系追踪实验中,胃窦和胃体峡部的 Bmi1 表达细胞在 6 个月内,双向地向腔侧和基底侧提供祖细胞。在胃类器官中,Bmi1 表达细胞也提供了祖细胞。Bmi1 表达细胞的消融导致小鼠胃和类器官中的胃上皮受损。在高剂量他莫昔芬诱导的胃黏膜损伤后,Bmi1 表达细胞谱系在他莫昔芬注射后 7 天内扩增并完全占据了胃窦和胃体的所有胃腺。在照射和乙酸诱导的胃黏膜损伤后,Bmi1 表达细胞也有助于再生。总之,Bmi1 是胃窦和胃体峡部的胃干细胞标志物。Bmi1 表达细胞具有干细胞潜能,无论是在生理条件下还是在胃黏膜损伤后的再生过程中。