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定义肠道中的干性等级:来自生物标志物和调控途径的证据。

Defining hierarchies of stemness in the intestine: evidence from biomarkers and regulatory pathways.

机构信息

Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; and.

Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; and Joint Department of Biomedical Engineering, University of North Carolina/North Carolina State University, Chapel Hill, North Carolina

出版信息

Am J Physiol Gastrointest Liver Physiol. 2014 Aug 1;307(3):G260-73. doi: 10.1152/ajpgi.00066.2014. Epub 2014 Jun 12.

Abstract

For decades, the rapid proliferation and well-defined cellular lineages of the small intestinal epithelium have driven an interest in the biology of the intestinal stem cells (ISCs) and progenitors that produce the functional cells of the epithelium. Recent and significant advances in ISC biomarker discovery have established the small intestinal epithelium as a powerful model system for studying general paradigms in somatic stem cell biology and facilitated elegant genetic and functional studies of stemness in the intestine. However, this newfound wealth of ISC biomarkers raises important questions of marker specificity. Furthermore, the ISC field must now begin to reconcile biomarker status with functional stemness, a challenge that is made more complex by emerging evidence that cellular hierarchies in the intestinal epithelium are more plastic than previously imagined, with some progenitor populations capable of dedifferentiating and functioning as ISCs following damage. In this review, we discuss the state of the ISC field in terms of biomarkers, tissue dynamics, and cellular hierarchies, and how these processes might be informed by earlier studies into signaling networks in the small intestine.

摘要

几十年来,小肠上皮细胞的快速增殖和明确的细胞谱系一直推动着人们对肠道干细胞 (ISCs) 和产生上皮功能细胞的祖细胞的生物学研究产生兴趣。最近在 ISC 生物标志物发现方面的重大进展确立了小肠上皮作为研究体干细胞生物学一般范例的强大模型系统,并促进了对肠道干性的精细遗传和功能研究。然而,这种新发现的 ISC 生物标志物提出了关于标记物特异性的重要问题。此外,ISC 领域现在必须开始将生物标志物状态与功能性干性联系起来,这一挑战变得更加复杂,因为有新的证据表明,肠道上皮细胞的细胞层次比以前想象的更具可塑性,一些祖细胞群在受到损伤后能够去分化并作为 ISC 发挥作用。在这篇综述中,我们讨论了 ISC 领域在生物标志物、组织动态和细胞层次方面的状况,以及这些过程如何通过早期对小肠信号网络的研究得到启发。

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