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本文引用的文献

1
The pan-ErbB negative regulator Lrig1 is an intestinal stem cell marker that functions as a tumor suppressor.pan-ErbB 阴性调节剂 Lrig1 是一种肠道干细胞标志物,具有肿瘤抑制作用。
Cell. 2012 Mar 30;149(1):146-58. doi: 10.1016/j.cell.2012.02.042.
2
Lrig1 controls intestinal stem-cell homeostasis by negative regulation of ErbB signalling.Lrig1 通过负向调控 ErbB 信号来控制肠道干细胞的自我更新。
Nat Cell Biol. 2012 Mar 4;14(4):401-8. doi: 10.1038/ncb2464.
3
Activation of two distinct Sox9-EGFP-expressing intestinal stem cell populations during crypt regeneration after irradiation.在辐射后隐窝再生过程中,两个不同的 Sox9-EGFP 表达肠干细胞群体被激活。
Am J Physiol Gastrointest Liver Physiol. 2012 May 15;302(10):G1111-32. doi: 10.1152/ajpgi.00519.2011. Epub 2012 Feb 23.
4
Identification of a cKit(+) colonic crypt base secretory cell that supports Lgr5(+) stem cells in mice.鉴定出一种 cKit(+) 结肠隐窝基底部分泌细胞,其在小鼠中支持 Lgr5(+) 干细胞。
Gastroenterology. 2012 May;142(5):1195-1205.e6. doi: 10.1053/j.gastro.2012.02.006. Epub 2012 Feb 11.
5
A basal gradient of Wnt and stem-cell number influences regional tumour distribution in human and mouse intestinal tracts.Wnt 和干细胞数量的基础梯度会影响人类和小鼠肠道的区域肿瘤分布。
Gut. 2013 Jan;62(1):83-93. doi: 10.1136/gutjnl-2011-301601. Epub 2012 Jan 27.
6
Tales from the crypt: the expanding role of slow cycling intestinal stem cells.从 crypt 中传出的故事:慢循环肠道干细胞作用的扩展。
Cell Stem Cell. 2012 Jan 6;10(1):2-4. doi: 10.1016/j.stem.2011.12.012.
7
MicroRNA-449a overexpression, reduced NOTCH1 signals and scarce goblet cells characterize the small intestine of celiac patients.miRNA-449a 的过表达、NOTCH1 信号的减少和杯状细胞的稀少是乳糜泻患者小肠的特征。
PLoS One. 2011;6(12):e29094. doi: 10.1371/journal.pone.0029094. Epub 2011 Dec 15.
8
Notch signaling modulates proliferation and differentiation of intestinal crypt base columnar stem cells.Notch 信号通路调节肠道隐窝基底部柱状干细胞的增殖和分化。
Development. 2012 Feb;139(3):488-97. doi: 10.1242/dev.070763. Epub 2011 Dec 21.
9
The intestinal stem cell markers Bmi1 and Lgr5 identify two functionally distinct populations.肠干细胞标志物 Bmi1 和 Lgr5 可识别出两个具有不同功能的群体。
Proc Natl Acad Sci U S A. 2012 Jan 10;109(2):466-71. doi: 10.1073/pnas.1118857109. Epub 2011 Dec 21.
10
Controlled gene expression in primary Lgr5 organoid cultures.在原代 Lgr5 类器官培养物中进行基因表达的控制。
Nat Methods. 2011 Dec 4;9(1):81-3. doi: 10.1038/nmeth.1802.

肠道干细胞中的主要信号通路。

Major signaling pathways in intestinal stem cells.

作者信息

Vanuytsel Tim, Senger Stefania, Fasano Alessio, Shea-Donohue Terez

机构信息

Mucosal Biology Research Center, University of Maryland School of Medicine, Baltimore, MD, USA.

出版信息

Biochim Biophys Acta. 2013 Feb;1830(2):2410-26. doi: 10.1016/j.bbagen.2012.08.006. Epub 2012 Aug 16.

DOI:10.1016/j.bbagen.2012.08.006
PMID:22922290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4408610/
Abstract

BACKGROUND

The discovery of markers to identify the intestinal stem cell population and the generation of powerful transgenic mouse models to study stem cell physiology have led to seminal discoveries in stem cell biology.

SCOPE OF REVIEW

In this review we give an overview of the current knowledge in the field of intestinal stem cells (ISCs) highlighting the most recent progress on markers defining the ISC population and pathways governing intestinal stem cell maintenance and differentiation. Furthermore we review their interaction with other stem cell related pathways. Finally we give an overview of alteration of these pathways in human inflammatory gastrointestinal diseases.

MAJOR CONCLUSIONS

We highlight the complex network of interactions occurring among different pathways and put in perspective the many layers of regulation that occur in maintaining the intestinal homeostasis.

GENERAL SIGNIFICANCE

Understanding the involvement of ISCs in inflammatory diseases can potentially lead to new therapeutic approaches to treat inflammatory GI pathologies such as IBD and celiac disease and could reveal the molecular mechanisms leading to the pathogenesis of dysplasia and cancer in inflammatory chronic conditions. This article is part of a Special Issue entitled Biochemistry of Stem Cells.

摘要

背景

用于鉴定肠道干细胞群体的标志物的发现以及用于研究干细胞生理学的强大转基因小鼠模型的建立,促成了干细胞生物学领域的重大发现。

综述范围

在本综述中,我们概述了肠道干细胞(ISC)领域的当前知识,重点介绍了定义ISC群体的标志物以及控制肠道干细胞维持和分化的途径方面的最新进展。此外,我们还综述了它们与其他干细胞相关途径的相互作用。最后,我们概述了这些途径在人类炎症性胃肠疾病中的改变。

主要结论

我们强调了不同途径之间发生的复杂相互作用网络,并阐述了维持肠道内环境稳定过程中发生的多层调控。

普遍意义

了解ISC在炎症性疾病中的作用可能会带来治疗炎症性胃肠疾病(如炎症性肠病和乳糜泻)的新治疗方法,并可能揭示导致炎症性慢性病发育异常和癌症发病机制的分子机制。本文是名为“干细胞生物化学”的特刊的一部分。