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酸在胃修复和癌症中的细胞可塑性和重编程的基础。

Acid and the basis for cellular plasticity and reprogramming in gastric repair and cancer.

机构信息

Division of Gastroenterology, Department of Internal Medicine, Washington University School of Medicine, 660 S. Euclid Avenue, St. Louis, MO, 63110, USA.

Department of Developmental Biology, Washington University School of Medicine, 660 S. Euclid Avenue, St. Louis, MO, 63110, USA.

出版信息

Nat Rev Gastroenterol Hepatol. 2018 May;15(5):257-273. doi: 10.1038/nrgastro.2018.5. Epub 2018 Feb 21.

Abstract

Subjected to countless daily injuries, the stomach still functions as a remarkably efficient digestive organ and microbial filter. In this Review, we follow the lead of the earliest gastroenterologists who were fascinated by the antiseptic and digestive powers of gastric secretions. We propose that it is easiest to understand how the stomach responds to injury by stressing the central role of the most important gastric secretion, acid. The stomach follows two basic patterns of adaptation. The superficial response is a pattern whereby the surface epithelial cells migrate and rapidly proliferate to repair erosions induced by acid or other irritants. The stomach can also adapt through a glandular response when the source of acid is lost or compromised (that is, the process of oxyntic atrophy). We primarily review the mechanisms governing the glandular response, which is characterized by a metaplastic change in cellular differentiation known as spasmolytic polypeptide-expressing metaplasia (SPEM). We propose that the stomach, like other organs, exhibits marked cellular plasticity: the glandular response involves reprogramming mature cells to serve as auxiliary stem cells that replace lost cells. Unfortunately, such plasticity might mean that the gastric epithelium undergoes cycles of differentiation and de-differentiation that increase the risk of accumulating cancer-predisposing mutations.

摘要

胃每天都会受到无数损伤,但仍能作为一个高效的消化器官和微生物过滤器发挥功能。在这篇综述中,我们追随最早对胃分泌物的杀菌和消化能力感到着迷的胃肠病学家的脚步。我们提出,通过强调最重要的胃液——胃酸的核心作用,就能最容易地理解胃对损伤的反应。胃遵循两种基本适应模式。表面反应是一种模式,其中表面上皮细胞迁移并迅速增殖,以修复由酸或其他刺激物引起的侵蚀。当胃酸的来源丢失或受损(即,壁细胞萎缩过程)时,胃还可以通过腺体反应进行适应。我们主要综述了控制腺体反应的机制,腺体反应的特征是细胞分化的一种可塑性变化,称为松弛多肽表达化生(SPEM)。我们提出,胃和其他器官一样,表现出明显的细胞可塑性:腺体反应涉及重新编程成熟细胞,使其充当替代丢失细胞的辅助干细胞。不幸的是,这种可塑性可能意味着胃上皮经历分化和去分化的循环,从而增加积累致癌突变的风险。

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