• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

发育生物学。肠道干细胞的区域特性——一个基因统领全局。

Developmental biology. Regional identity of gut stem cells--one gene to rule them all.

机构信息

Division of Developmental Biology and Division of Endocrinology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229-3039, USA.

出版信息

Nat Rev Gastroenterol Hepatol. 2015 Mar;12(3):125-6. doi: 10.1038/nrgastro.2015.22. Epub 2015 Feb 3.

DOI:10.1038/nrgastro.2015.22
PMID:25645971
Abstract

The stem cells in the stomach and intestine are regulated by different signalling pathways and give rise to entirely different specialized lineages. A study by Simmini and colleagues suggests that the organ-specific identity of gastrointestinal stem cells is regulated by one transcription factor, Cdx2.

摘要

胃和肠道中的干细胞受不同信号通路的调控,并产生完全不同的特化谱系。Simmini 及其同事的一项研究表明,胃肠道干细胞的器官特异性由一个转录因子 Cdx2 调控。

相似文献

1
Developmental biology. Regional identity of gut stem cells--one gene to rule them all.发育生物学。肠道干细胞的区域特性——一个基因统领全局。
Nat Rev Gastroenterol Hepatol. 2015 Mar;12(3):125-6. doi: 10.1038/nrgastro.2015.22. Epub 2015 Feb 3.
2
Transformation of intestinal stem cells into gastric stem cells on loss of transcription factor Cdx2.转录因子Cdx2缺失时肠道干细胞向胃干细胞的转化
Nat Commun. 2014 Dec 11;5:5728. doi: 10.1038/ncomms6728.
3
CDX1 confers intestinal phenotype on gastric epithelial cells via induction of stemness-associated reprogramming factors SALL4 and KLF5.CDX1 通过诱导干性相关重编程因子 SALL4 和 KLF5 赋予胃上皮细胞肠表型。
Proc Natl Acad Sci U S A. 2012 Dec 11;109(50):20584-9. doi: 10.1073/pnas.1208651109. Epub 2012 Oct 29.
4
Expression of Claudin-2 in intestinal metaplastic mucosa of Cdx2-transgenic mouse stomach.Claudin-2在Cdx2转基因小鼠胃肠化生黏膜中的表达
Scand J Gastroenterol. 2010 Nov;45(11):1273-80. doi: 10.3109/00365521.2010.501522. Epub 2010 Jul 5.
5
The intestine-specific homeobox gene Cdx2 induces expression of the basic helix-loop-helix transcription factor Math1.肠道特异性同源盒基因Cdx2可诱导碱性螺旋-环-螺旋转录因子Math1的表达。
Differentiation. 2006 Jul;74(6):313-21. doi: 10.1111/j.1432-0436.2006.00074.x.
6
Cdx2 initiates histodifferentiation of the midgut endoderm.Cdx2启动中肠内胚层的组织分化。
FEBS Lett. 2008 Jul 23;582(17):2555-60. doi: 10.1016/j.febslet.2008.06.024. Epub 2008 Jun 23.
7
SOX2 redirects the developmental fate of the intestinal epithelium toward a premature gastric phenotype.SOX2 将肠上皮的发育命运重定向为早期胃表型。
J Mol Cell Biol. 2012 Dec;4(6):377-85. doi: 10.1093/jmcb/mjs030. Epub 2012 Jun 7.
8
Expression of Cdx1 and Cdx2 mRNAs and relevance of this expression to differentiation in human gastrointestinal mucosa--with special emphasis on participation in intestinal metaplasia of the human stomach.Cdx1和Cdx2 mRNA的表达及其与人类胃肠道黏膜分化的相关性——特别强调其在人胃肠化生中的作用
Gastric Cancer. 2001;4(4):185-91. doi: 10.1007/pl00011741.
9
Generation of Mouse and Human Organoid-Forming Intestinal Progenitor Cells by Direct Lineage Reprogramming.通过直接谱系重编程生成小鼠和人类类器官形成肠祖细胞。
Cell Stem Cell. 2017 Oct 5;21(4):456-471.e5. doi: 10.1016/j.stem.2017.08.020. Epub 2017 Sep 21.
10
Down-regulation of a gastric transcription factor, Sox2, and ectopic expression of intestinal homeobox genes, Cdx1 and Cdx2: inverse correlation during progression from gastric/intestinal-mixed to complete intestinal metaplasia.胃转录因子Sox2的下调以及肠同源盒基因Cdx1和Cdx2的异位表达:从胃/肠混合化生到完全肠化生进展过程中的负相关。
J Cancer Res Clin Oncol. 2004 Mar;130(3):135-45. doi: 10.1007/s00432-003-0519-6. Epub 2003 Dec 4.

引用本文的文献

1
Induced organoids derived from patients with ulcerative colitis recapitulate colitic reactivity.诱导的类器官源自溃疡性结肠炎患者,可重现结肠炎反应性。
Nat Commun. 2021 Jan 11;12(1):262. doi: 10.1038/s41467-020-20351-5.
2
Developmental History Provides a Roadmap for the Emergence of Tumor Plasticity.发育史为肿瘤可塑性的出现提供了路线图。
Dev Cell. 2018 Mar 26;44(6):679-693.e5. doi: 10.1016/j.devcel.2018.02.024.
3
Plasticity in the lung: making and breaking cell identity.肺的可塑性:细胞身份的塑造与重塑

本文引用的文献

1
Transformation of intestinal stem cells into gastric stem cells on loss of transcription factor Cdx2.转录因子Cdx2缺失时肠道干细胞向胃干细胞的转化
Nat Commun. 2014 Dec 11;5:5728. doi: 10.1038/ncomms6728.
2
CDX2 can be regulated through the signalling pathways activated by IL-6 in gastric cells.CDX2可通过胃细胞中由IL-6激活的信号通路进行调控。
Biochim Biophys Acta. 2014 Sep;1839(9):785-92. doi: 10.1016/j.bbagrm.2014.06.009. Epub 2014 Jun 19.
3
Adult stem cells in the small intestine are intrinsically programmed with their location-specific function.
Development. 2017 Mar 1;144(5):755-766. doi: 10.1242/dev.143784.
小肠中的成体干细胞在本质上被编程为具有其特定位置的功能。
Stem Cells. 2014 May;32(5):1083-91. doi: 10.1002/stem.1655.
4
Gastric intestinal metaplasia revisited: function and regulation of CDX2.胃肠上皮化生再探讨:CDX2 的功能与调控。
Trends Mol Med. 2012 Sep;18(9):555-63. doi: 10.1016/j.molmed.2012.07.006. Epub 2012 Aug 4.
5
SOX2 redirects the developmental fate of the intestinal epithelium toward a premature gastric phenotype.SOX2 将肠上皮的发育命运重定向为早期胃表型。
J Mol Cell Biol. 2012 Dec;4(6):377-85. doi: 10.1093/jmcb/mjs030. Epub 2012 Jun 7.
6
Cdx2 determines the fate of postnatal intestinal endoderm.Cdx2 决定了出生后肠道内胚层的命运。
Development. 2012 Feb;139(3):465-74. doi: 10.1242/dev.070722. Epub 2011 Dec 21.
7
Sox2(+) adult stem and progenitor cells are important for tissue regeneration and survival of mice.Sox2(+) 成年干细胞和祖细胞对小鼠的组织再生和存活很重要。
Cell Stem Cell. 2011 Oct 4;9(4):317-29. doi: 10.1016/j.stem.2011.09.001.
8
Establishment of intestinal identity and epithelial-mesenchymal signaling by Cdx2.通过Cdx2建立肠道特征及上皮-间充质信号传导。
Dev Cell. 2009 Apr;16(4):588-99. doi: 10.1016/j.devcel.2009.02.010.
9
The ParaHox gene cluster is an evolutionary sister of the Hox gene cluster.副同源盒基因簇是同源盒基因簇在进化上的姐妹。
Nature. 1998 Apr 30;392(6679):920-2. doi: 10.1038/31933.
10
Homeosis and intestinal tumours in Cdx2 mutant mice.Cdx2突变小鼠中的同源异型现象与肠道肿瘤
Nature. 1997 Mar 6;386(6620):84-7. doi: 10.1038/386084a0.