p53 基因突变使巴雷特食管中的鳞柱交界祖细胞偏向于发育不良而非移行症

IF 23 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Gut Pub Date : 2024-10-01 DOI:10.1136/gutjnl-2024-332095
Guodong Lian, Ermanno Malagola, Chengguo Wei, Qiongyu Shi, Junfei Zhao, Masahiro Hata, Hiroki Kobayashi, Yosuke Ochiai, Biyun Zheng, Xiaofei Zhi, Feijing Wu, Ruhong Tu, Osmel Companioni Nápoles, Wenjing Su, Leping Li, Changqing Jing, Man Chen, Leah Zamechek, Richard Friedman, Karol Nowicki-Osuch, Michael Quante, Jianwen Que, Timothy C Wang
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Sorted metaplastic cells grew poorly with no progression to dysplasia, while mutant progenitors gave rise to dysplasia in orthotopic transplantation. Computational analyses indicated that p53 mutation inhibited stem cell differentiation through Notch activation. Conclusions p53 mutation contributes to BE progression by increasing expansion and fitness of undifferentiated cardia progenitors and preventing their differentiation towards metaplasia. Data are available on reasonable request. 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引用次数: 0

摘要

背景 虽然p53突变发生在巴雷特食管(BE)进展为食管腺癌(EAC)的早期,但它们在胃贲门干细胞中的作用仍不清楚。目的 本研究探讨了p53突变对贲门祖细胞在BE进展为EAC过程中的命运和功能的影响,尤其是在慢性损伤的胁迫下。设计 我们利用携带Trp53突变(R172H)的BE小鼠模型(L2-IL1β)研究p53对Cck2r+贲门祖细胞的影响。我们采用品系追踪、病理分析、类器官培养、单细胞RNA测序(scRNA-seq)和计算分析来研究祖细胞行为、分化模式和肿瘤进展的变化。此外,我们还对分选的变异和突变祖细胞进行了正位移植,以评估它们在体内的致瘤潜力。结果 p53突变是扩增祖细胞和抑制祖细胞向扁平化分化的开关,但仅在慢性损伤时起作用。在L2-IL1β小鼠中,p53突变增加了祖细胞的扩增和系谱追踪,并从扁平化转变为发育不良。scRNA-seq发现,发育不良细胞直接来自突变祖细胞,而不是通过扁平化发展而来。在体外,p53突变增强了BE祖细胞的器官形成效率、生长、DNA损伤抵抗力和非整倍体进展。分选的变性细胞生长不良,没有发展为发育不良,而突变祖细胞在正位移植中会出现发育不良。计算分析表明,p53突变通过激活Notch抑制干细胞分化。结论 p53突变通过增加未分化贲门祖细胞的扩增和适应性,阻止其向移行分化,从而促进BE的进展。如有合理要求,可提供相关数据。与研究相关的所有数据均包含在文章中或作为在线补充信息上传。
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p53 mutation biases squamocolumnar junction progenitor cells towards dysplasia rather than metaplasia in Barrett’s oesophagus
Background While p53 mutations occur early in Barrett’s oesophagus (BE) progression to oesophageal adenocarcinoma (EAC), their role in gastric cardia stem cells remains unclear. Objective This study investigates the impact of p53 mutation on the fate and function of cardia progenitor cells in BE to EAC progression, particularly under the duress of chronic injury. Design We used a BE mouse model (L2-IL1β) harbouring a Trp53 mutation (R172H) to study the effects of p53 on Cck2r+ cardia progenitor cells. We employed lineage tracing, pathological analysis, organoid cultures, single-cell RNA sequencing (scRNA-seq) and computational analyses to investigate changes in progenitor cell behaviour, differentiation patterns and tumour progression. Additionally, we performed orthotopic transplantation of sorted metaplastic and mutant progenitor cells to assess their tumourigenic potential in vivo. Results The p53 mutation acts as a switch to expand progenitor cells and inhibit their differentiation towards metaplasia, but only amidst chronic injury. In L2-IL1β mice, p53 mutation increased progenitors expansion and lineage-tracing with a shift from metaplasia to dysplasia. scRNA-seq revealed dysplastic cells arise directly from mutant progenitors rather than progressing through metaplasia. In vitro, p53 mutation enhanced BE progenitors’ organoid-forming efficiency, growth, DNA damage resistance and progression to aneuploidy. Sorted metaplastic cells grew poorly with no progression to dysplasia, while mutant progenitors gave rise to dysplasia in orthotopic transplantation. Computational analyses indicated that p53 mutation inhibited stem cell differentiation through Notch activation. Conclusions p53 mutation contributes to BE progression by increasing expansion and fitness of undifferentiated cardia progenitors and preventing their differentiation towards metaplasia. Data are available on reasonable request. All data relevant to the study are included in the article or uploaded as online supplemental information.
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来源期刊
Gut
Gut 医学-胃肠肝病学
CiteScore
45.70
自引率
2.40%
发文量
284
审稿时长
1.5 months
期刊介绍: Gut is a renowned international journal specializing in gastroenterology and hepatology, known for its high-quality clinical research covering the alimentary tract, liver, biliary tree, and pancreas. It offers authoritative and current coverage across all aspects of gastroenterology and hepatology, featuring articles on emerging disease mechanisms and innovative diagnostic and therapeutic approaches authored by leading experts. As the flagship journal of BMJ's gastroenterology portfolio, Gut is accompanied by two companion journals: Frontline Gastroenterology, focusing on education and practice-oriented papers, and BMJ Open Gastroenterology for open access original research.
期刊最新文献
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