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代谢调节剂 ERRγ 调控胃干细胞向分泌胃酸的壁细胞分化。

Metabolic regulator ERRγ governs gastric stem cell differentiation into acid-secreting parietal cells.

机构信息

Section of Gastroenterology, Department of Medicine, Baylor College of Medicine, Houston, TX 77030, USA; Division of Biomedical and Biological Sciences, Washington University, St. Louis, MO 63130, USA; Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.

Section of Gastroenterology, Department of Medicine, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Cell Stem Cell. 2024 Jun 6;31(6):886-903.e8. doi: 10.1016/j.stem.2024.04.016. Epub 2024 May 10.

DOI:10.1016/j.stem.2024.04.016
PMID:38733994
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11162331/
Abstract

Parietal cells (PCs) produce gastric acid to kill pathogens and aid digestion. Dysregulated PC census is common in disease, yet how PCs differentiate is unclear. Here, we identify the PC progenitors arising from isthmal stem cells, using mouse models and human gastric cells, and show that they preferentially express cell-metabolism regulator and orphan nuclear receptor Estrogen-related receptor gamma (Esrrg, encoding ERRγ). Esrrg expression facilitated the tracking of stepwise molecular, cellular, and ultrastructural stages of PC differentiation. Esrrg lineage tracing revealed that Esrrg expression commits progenitors to differentiate into mature PCs. scRNA-seq indicated the earliest Esrrg+ PC progenitors preferentially express SMAD4 and SP1 transcriptional targets and the GTPases regulating acid-secretion signal transduction. As progenitors matured, ERRγ-dependent metabolic transcripts predominated. Organoid and mouse studies validated the requirement of ERRγ for PC differentiation. Our work chronicles stem cell differentiation along a single lineage in vivo and suggests ERRγ as a therapeutic target for PC-related disorders.

摘要

壁细胞(PCs)产生胃酸以杀死病原体并帮助消化。PC 计数失调在疾病中很常见,但 PC 如何分化尚不清楚。在这里,我们使用小鼠模型和人类胃细胞鉴定了起源于峡部干细胞的 PC 祖细胞,并表明它们优先表达细胞代谢调节剂和孤儿核受体雌激素相关受体γ(Esrrg,编码 ERRγ)。Esrrg 的表达促进了对 PC 分化的逐步分子、细胞和超微结构阶段的跟踪。Esrrg 谱系示踪显示,Esrrg 表达使祖细胞分化为成熟的 PCs。scRNA-seq 表明,最早的 Esrrg+ PC 祖细胞优先表达 SMAD4 和 SP1 转录靶点以及调节胃酸分泌信号转导的 GTPases。随着祖细胞的成熟,依赖 ERRγ 的代谢转录本占主导地位。类器官和小鼠研究验证了 ERRγ 对 PC 分化的要求。我们的工作描述了体内沿单一谱系的干细胞分化,并提出 ERRγ 作为与 PC 相关疾病的治疗靶点。

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